The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained. Concept introduction: E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism. E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step. Example, Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- − OTs group of the alkyl tosylates. Curved arrows are used for drawing the mechanism of reaction. To draw: the product of the given elimination reaction.

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Answer 1

Question

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

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Answer 2

Question

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

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Answer 3

Question

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

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Answer 4

Question

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

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Answer 5

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

Answer 6

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

Answer 7

Chapter 8.6, Problem 11ATS

Interpretation Introduction

Interpretation:

The alkene compound produced by the given reaction is needed to be drawn and whether the mechanism for this reaction is concerted or stepwise should be explained.

Concept introduction:

E1 reaction is a unimolecular elimination reaction to produce alkene compounds in which carbocation is formed as an intermediate and it has stepwise mechanism.

E2 reaction is a concerted bimolecular elimination reaction in which alkene compound is formed in a single step.

Example,

Alkenes are formed when alkyl tosylates are treated with strong base via eliminating one β-proton and α- −OTs group of the alkyl tosylates.

Curved arrows are used for drawing the mechanism of reaction.

To draw: the product of the given elimination reaction.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 8.3 - Prob. 1LTS Ch. 8.3 - Prob. 1PTS Ch. 8.3 - Prob. 2ATS Ch. 8.3 - Prob. 3ATS Ch. 8.3 - Prob. 4CC Ch. 8.4 - Prob. 2LTS Ch. 8.4 - Prob. 5PTS Ch. 8.4 - Prob. 6ATS Ch. 8.5 - Prob. 3LTS Ch. 8.5 - Prob. 7PTS

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Chapter 8 Solutions