(a) Interpretation: The curved-arrow mechanism for the given reaction is to be predicted. Concept introduction: Amines ( RNH 2 ) or ammonia react with carbonyl compounds such as aldehyde ( RHC = O ) and ketone ( R 2 C = O ) to form imine bond ( − C = N − ) . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

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Answer 1

Question

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

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Answer 2

Question

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

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Answer 3

Question

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

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Answer 4

Question

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

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Answer 5

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

Answer 6

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 7

Chapter 27, Problem 27.77AP

Interpretation Introduction

(a)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The curved-arrow mechanism for the given reaction is to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

Amines $(RNH2)$ or ammonia react with carbonyl compounds such as aldehyde $(RHC=O)$ and ketone $(R2C=O)$ to form imine bond $(−C=N−)$ . The imine derivative is also termed as Schiff base. A water molecule is eliminated in this reaction.

Answer 12

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

Answer 13

Interpretation Introduction

(d)

Interpretation:

The curved-arrow mechanism for the given reaction has to be predicted.

Concept introduction:

The rearrangement in which acyl azides $(RCO−N3)$ undergoes a reaction to form the amines is known as Curtius rearrangement. The acyls azide is heated in benzene or toluene, inert solvent, which results in a loss of nitrogen to form isocyanate $(R−N=C=O)$ . The acid or base hydrolysis converts the isocyanate products into amines.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. 27 - Prob. 27.1P Ch. 27 - Prob. 27.2P Ch. 27 - Prob. 27.3P Ch. 27 - Prob. 27.4P Ch. 27 - Prob. 27.5P Ch. 27 - Prob. 27.6P Ch. 27 - Prob. 27.8P Ch. 27 - Prob. 27.9P Ch. 27 - Prob. 27.10P Ch. 27 - Prob. 27.11P

Solution Summary: The author explains that the curved-arrow mechanism for the given reaction is to be predicted.

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Chapter 27 Solutions