Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated. Concept introduction: In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

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Answer 1

Question

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

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Answer 2

Question

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

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Answer 3

Question

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

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Answer 4

Question

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

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Answer 5

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

Answer 6

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

Answer 7

Chapter 22.7A, Problem 22.18P

Interpretation Introduction

Interpretation:

Mechanism for the aldol condensation of cyclohexanone is to be proposed. Whether the equiulibrium favor the reactant or the product is to be stated.

Concept introduction:

In base-catalysed aldol condensation, nucleophilic addition of an enolate ion takes place on a carbonyl group. In first step, an alpha proton is removed to produce enolate ion. It adds to the carbonyl group. In the next step, protonation of alkoxide gives the aldol product.

Answer 8

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Answer 10

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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 aldol condensation of cyclohexanone.

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