The detailed mechanism for the specified reaction is to be drawn. Concept introduction: The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

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Answer 1

Question

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

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Answer 2

Question

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

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Answer 3

Question

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

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Answer 4

Question

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

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Answer 5

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

Answer 6

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

Answer 7

Chapter 21, Problem 21.6P

Interpretation Introduction

Interpretation:

The detailed mechanism for the specified reaction is to be drawn.

Concept introduction:

The acid anhydride reacts with the nucleophilic amine produces an amide. The amine acts as the nucleophile in the nucleophilic addition step. Two equivalent of amine is required in the reaction, the first equivalent is used as a nucleophile and the second equivalent is used as a base. The carboxylate anion is the leaving group in the nucleophilic elimination step.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 21 - Prob. 21.1P Ch. 21 - Prob. 21.2P Ch. 21 - Prob. 21.3P Ch. 21 - Prob. 21.4P Ch. 21 - Prob. 21.5P Ch. 21 - Prob. 21.6P Ch. 21 - Prob. 21.7P Ch. 21 - Prob. 21.8P Ch. 21 - Prob. 21.9P Ch. 21 - Prob. 21.10P

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Chapter 21 Solutions