A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed. Concept introduction: Grignard reagent is used to generate R − , carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 1

Question

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 2

Question

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 3

Question

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Expert Solution & Answer

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Answer 4

Question

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

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Answer 5

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 6

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 7

Chapter 21.9, Problem 21.27P

Interpretation Introduction

Interpretation:

A mechanism for the reaction of propanoyl chloride with 2 moles of phenylmagnesium bromide is to be proposed.

Concept introduction:

Grignard reagent is used to generate R−, carbanion which attack on electron deficient centre. Carbonyl group that has good leaving group gives substituted product. This reagent is used to convert carbonyl group into alcohol.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 21.2F - Name the following carboxylic acid derivatives,...Ch. 21.4A - Prob. 21.2P Ch. 21.4A - Prob. 21.3P Ch. 21.4A - Prob. 21.4P Ch. 21.5C - Prob. 21.7P Ch. 21.6 - When ethyl 4-hydroxybutyrate is heated in the...Ch. 21.6 - Propose a mechanism for the following ring-opening...Ch. 21.6 - Prob. 21.15P Ch. 21.7B - Prob. 21.16P Ch. 21.7C - Prob. 21.19P

Solution Summary: The author proposes a mechanism for the reaction of propanoyl chloride with 2 moles of phenylaminium bromide.

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Chapter 21 Solutions