A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed. Concept introduction: In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

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Answer 1

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Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

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Answer 2

Question

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

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Answer 3

Question

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

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Answer 4

Question

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

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Answer 5

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

Answer 6

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

Answer 7

Chapter 22.14, Problem 22.41P

Interpretation Introduction

Interpretation:

A mechanism for the crossed Claisen condensation between ethyl acetate and ethyl benzoate is to be proposed.

Concept introduction:

In crossed claisen condensation, an ester without the alpha hydrogen adds to a solution of the alkoxide base. The reaction of ester with alpha hydrogens to this solution is slow. In this reaction, the electrophilic component is ester without alpha hydrogens.

Answer 8

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Answer 11

Ch. 22.2A - Prob. 22.2P Ch. 22.4 - Without looking back, propose a mechanism for the...Ch. 22.4 - Prob. 22.8P Ch. 22.4 - Prob. 22.9P Ch. 22.5A - Prob. 22.10P Ch. 22.5A - Prob. 22.11P Ch. 22.5B - Prob. 22.12P Ch. 22.5B - Predict the products of the following reactions....Ch. 22.5B - Which compounds will give positive iodoform tests?...Ch. 22.5C - Propose a mechanism for the acid-catalyzed...

Solution Summary: The author explains the mechanism for the crossed claisen condensation between ethyl acetate and

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