The complete, detailed mechanism for the given reaction is to be predicted. Concept introduction: It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH 3 ) 3 COK ; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

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Answer 1

Question

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

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Answer 2

Question

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

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Answer 3

Question

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

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Answer 4

Question

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

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Answer 5

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

Answer 6

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

Answer 7

Chapter 20, Problem 20.60P

Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be predicted.

Concept introduction:

It is a nucleophilic addition-elimination reaction. The reaction is carried out under basic condition (CH3)3COK; hence no strong base appeared in the reaction. The carbonyl compound contains an alkyl group with a chlorine group treated with nitromethane in the presence of strong base t-butoxide. Here the nitromethane acts as a nucleophile. The mechanism involved two steps, nucleophilic addition followed by nucleophilic elimination.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 20 - Prob. 20.1P Ch. 20 - Prob. 20.2P Ch. 20 - Prob. 20.3P Ch. 20 - Prob. 20.4P Ch. 20 - Prob. 20.5P Ch. 20 - Prob. 20.6P Ch. 20 - Prob. 20.7P Ch. 20 - Prob. 20.8P Ch. 20 - Prob. 20.9P Ch. 20 - Prob. 20.10P

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