The product with detailed mechanism for the given reaction is to be drawn. Concept introduction: Like aldehydes or ketones , primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via S N 2 mechanism.

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Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

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Answer 2

Question

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

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Answer 3

Question

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

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Answer 4

Question

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

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Answer 5

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

Answer 6

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

Answer 7

Chapter 10, Problem 10.40P

Interpretation Introduction

Interpretation:

The product with detailed mechanism for the given reaction is to be drawn.

Concept introduction:

Like aldehydes or ketones, primary or secondary amides can also act as good nucleophiles. In an amide, the deprotonation of amide nitrogen forms an anion where the negative charge is on the nitrogen atom. This negatively charged nitrogen atom is strongly nucleophilic and can undergo alkylation reaction with primary alkyl halide via SN2 mechanism.

Answer 8

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Answer 10

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Answer 11

Ch. 10 - Prob. 10.1P Ch. 10 - Prob. 10.2P Ch. 10 - Prob. 10.3P Ch. 10 - Prob. 10.4P Ch. 10 - Prob. 10.5P Ch. 10 - Prob. 10.6P Ch. 10 - Prob. 10.7P Ch. 10 - Prob. 10.8P Ch. 10 - Prob. 10.9P Ch. 10 - Prob. 10.10P

Solution Summary: The author explains that primary or secondary amides act as good nucleophiles. The first reagent is the strong base NaH, suggesting the proton transfer reaction.

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Chapter 10 Solutions