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Nucleophilic-Aromatic-Substitutions

Last updated July 1, 2022

nucleophilic-substitutions

NAS

https://www.masterorganicchemistry.com/2018/08/20/nucleophilic-aromatic-substitution-nas/

Ex

Ex

https://en.wikipedia.org/wiki/Nucleophilic_aromatic_substitution

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Alkane-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Iodine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Alkoxide-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrite-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Chlorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Fluorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Sulfonate-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Para-X-Alkoxide-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Para-X-Iodine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Phosphonate-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Alkane-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Chlorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Fluorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrite-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Chlorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Iodine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Phosphonate-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Chlorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Phosphonate-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R10 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrite-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrite-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Bromine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Iodine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Alkane-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Bromine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Vicarious-Nucleophilic-Substitution-Para-X-Bromine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Alkane-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Bromine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carbonyl-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Alkane-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Iodine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Phosphonate-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

Condition to enforce:

R4 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Phosphonate-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Iodine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carboxyl-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Chlorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Chlorine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Chlorine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Phosphonate-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Alkoxide-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Nitrite-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carboxyl-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Sulfonate-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrile-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Iodine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Alkane-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrile-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrite-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Chlorine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Alkane-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrile-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Nitric-Acid-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Fluorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Sulfonate-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carboxyl-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Thiolate-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

Condition to enforce:

R4 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Vicarious-Nucleophilic-Substitution-Para-X-Sulfonate-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Thiolate-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Bromine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Chihibabin-Reaction

References:
โ€ƒ[0]โ€‚ Chichibabin reaction - Wikipedia

Condition to enforce:

R1 = L-A, A-Aromatic-Carbon
R2 = L-A, A-Aromatic-Carbon
R3 = L-A, A-Aromatic-Carbon
R4 = L-A, A-Aromatic-Carbon

image

# Vicarious-Nucleophilic-Substitution-Para-X-Thiolate-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrile-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Alkane-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Bromine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Bromine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Alkane-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Alkoxide-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Pyridine-N-Oxide-Chlorination-Ortho

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Phosphonate-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R10 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Pyridine-N-Oxide-Chlorination-Para

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Iodine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Vicarious-Nucleophilic-Substitution-Para-X-Iodine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrite-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Alkane-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Alkane-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Iodine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrile-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrite-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Carboxyl-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Nitrite-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carbonyl-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Thiolate-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Bromine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Bromine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrile-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Alkane-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrite-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Alkoxide-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Carboxyl-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Phosphonate-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Carboxyl-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrite-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Phosphonate-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Bromine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Fluorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Chlorine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Nitrite-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Vicarious-Nucleophilic-Substitution-Para-X-Sulfonate-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Iodine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Nitric-Acid-Lg-Fluorine

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Chlorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Vicarious-Nucleophilic-Substitution-Para-X-Bromine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Alkane-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrile-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Alkane-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Iodine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Phosphonate-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R10 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Alkane-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrile-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrile-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrite-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

Condition to enforce:

R4 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Vicarious-Nucleophilic-Substitution-Para-X-Iodine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Sulfonate-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Nitric-Acid-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Vicarious-Nucleophilic-Substitution-Para-X-Thiolate-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carboxyl-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Sulfonate-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Alkane-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Phosphonate-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Alkane-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Thiolate-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Fluorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Chlorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Phosphonate-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Alkoxide-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Phosphonate-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Alkane-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Bromine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Fluorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrile-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Iodine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Alkane-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Phosphonate-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Alkoxide-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Alkoxide-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Nitrite-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Phosphonate-and-EWG2-Phosphonate-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R10 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Bromine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Fluorine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Iodine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrile-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Phosphonate-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Phosphonate-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R9 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Alkane-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Nitrite-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Iodine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carbonyl-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Phosphonate-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Nitrite-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Chlorine-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Sulfonate-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Vicarious-Nucleophilic-Substitution-Para-X-Chlorine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Nitrile-Lg-Iodine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Para-X-Chlorine-and-EWG-Nitrile

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A

image

# Nucleophilic-Aromatic-Substitution-Lg-Fluorine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Fluorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Chlorine-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image

# Substituted-Pyridine-Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ Weickgenannt_Jun_12.pdf

Condition to enforce:

R4 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrite-and-EWG2-Phosphonate-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Bromine-and-EWG-Carboxyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Vicarious-Nucleophilic-Substitution-Para-X-Thiolate-and-EWG-Carbonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Iodine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Bromine-and-Nu-Hydroxyl

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Para-Lg-Chlorine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carboxyl-and-EWG2-Carboxyl-Lg-Sulfonate

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Chlorine-and-Nu-Alkoxide

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Carbonyl-and-EWG2-Carbonyl-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group
R8 = H, A-Aromatic-Carbon, A-Aliphatic-Carbon, Vinyl-Group

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Nitric-Acid-Lg-Bromine

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Lg-Bromine-and-Nu-Thiolate

References:
โ€ƒ[0]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[1]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[2]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[3]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne
โ€ƒ[4]โ€‚ Explain why the trifluoromethyl (CF_3) group is meta directing in electrophilic aromatic substitution. What would you expect CF_3 to be activating or deactivating? Why? Can some one PLEASE help me!!!!! Thanks? | Socratic

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Alpha-Acid-EWG1-Nitrile-and-EWG2-Phosphonate-Lg-Chlorine

References:
โ€ƒ[0]โ€‚ Acetoacetic-Ester Synthesis
โ€ƒ[1]โ€‚ Substituted carbonyl compound synthesis by alkylation or condensation
โ€ƒ[2]โ€‚ Malonic Ester Synthesis
โ€ƒ[3]โ€‚ Carbonyl alpha-substitution reactions - Wikipedia

Condition to enforce:

R1 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R3 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R5 = L-A, A-Aliphatic-Carbon, H, Nitrite, Nitrile, Chlorine, Bromine, Iodine, Fluorine, Halocarbon
R6 = H, A-Aliphatic-Carbon
R7 = A-Aliphatic-Carbon, A-Aromatic-Carbon
R8 = A-Aliphatic-Carbon, A-Aromatic-Carbon

At least one logic:

Molecule conditions:
list_of_labels = R1, R3, R5
list_of_matching = (NO2L, Nitrite), (C#N[L], Nitrile), (ClL, Chlorine), (BrL, Bromine), (IL, Iodine), (FL, Fluorine), (CX3L, Halocarbon)

image

# Nucleophilic-Aromatic-Substitution-Pyridine-Ortho-Lg-Bromine-and-Nu-Amino

References:
โ€ƒ[0]โ€‚ organic chemistry - Why does nucleophilic aromatic substitution occur at C-2 and C-4 of pyridine? - Chemistry Stack Exchange
โ€ƒ[1]โ€‚ Nucleophilic Aromatic Substitution: Introduction and Mechanism
โ€ƒ[2]โ€‚ 16.7: Nucleophilic Aromatic Substitution - Chemistry LibreTexts
โ€ƒ[3]โ€‚ Nucleophilic Aromatic Substitution - Chemistry Steps
โ€ƒ[4]โ€‚ Organic chemistry 29: Aromaticity - nucleophilic aromatic substitution, benzyne

Condition to enforce:

R5 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon, Vinyl-Group-No-Oxygen, A-Alkoxide, Hydroxyl, A-Aliphatic-Nitrogen

image

# Vicarious-Nucleophilic-Substitution-Ortho-X-Thiolate-and-EWG-Sulfonyl

References:
โ€ƒ[0]โ€‚ Vicarious nucleophilic substitution - Wikipedia
โ€ƒ[1]โ€‚ Just a moment…

Condition to enforce:

R1 = L-A
R2 = L-A
R3 = L-A
R4 = L-A
R5 = L-A
R6 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon
R7 = H, A-Aliphatic-Carbon, A-Aromatic-Carbon

image


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