The stepwise mechanism for the given reaction is to be drawn. Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β -ketoester.

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Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

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Answer 2

Question

Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

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Answer 3

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Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

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Answer 4

Question

Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

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Answer 5

Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

Answer 6

Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

Answer 7

Chapter 22, Problem 54P

Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

Answer 8

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Answer 11

Ch. 22.1 - Prob. 1P Ch. 22.1 - Prob. 2P Ch. 22.1 - Problem 24.3 What unsaturated carbonyl compound is...Ch. 22.1 - Prob. 4P Ch. 22.1 - Prob. 5P Ch. 22.2 - Prob. 6P Ch. 22.2 - Problem 24.7 Draw the products formed in each...Ch. 22.4 - Prob. 15P Ch. 22.4 - Prob. 16P Ch. 22.5 - Problem 24.16 What ester is formed when each...

Solution Summary: The author explains that the stepwise mechanism for the given reaction is shown in Figure 1, Figure 2, and Figure 3.

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Chapter 22 Solutions