A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained. Concept introduction: In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants. In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

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Answer 1

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Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

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Answer 2

Question

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

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Answer 3

Question

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

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Answer 4

Question

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

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Answer 5

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

Answer 6

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

Answer 7

Chapter 21, Problem 21.63P

Interpretation Introduction

Interpretation:

A crossed Claisen reaction between methyl propionate and methyl acetate produces a mixture of products and so is not synthetically useful. The reason of the reaction between methyl 2-propionate and methyl acetate, is synthetically useful, is to be explained.

Concept introduction:

In a Claisen condensation reaction, an ester with at least two α protons is treated with a strong base, followed by acid workup, to produce β- keto ester. In these reactions, the base deprotonates the α carbon of one ester to produce an ester enolate anion, which acts as a nucleophile and attacks the carbonyl carbon of the second ester. The nucleophilic addition-elimination equilibrium favors reactants.

In a crossed Claisen condensation reaction, the enolate anion that acts as the nucleophile derives from an ester that is different from the ester it attacks.

Answer 8

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Answer 11

Ch. 21 - Prob. 21.1P Ch. 21 - Prob. 21.2P Ch. 21 - Prob. 21.3P Ch. 21 - Prob. 21.4P Ch. 21 - Prob. 21.5P Ch. 21 - Prob. 21.6P Ch. 21 - Prob. 21.7P Ch. 21 - Prob. 21.8P Ch. 21 - Prob. 21.9P Ch. 21 - Prob. 21.10P

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