s -cis conformation of the given diene is to be drawn. Concept introduction: The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s -cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s -cis conformation.

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Answer 1

Question

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

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Answer 2

Question

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

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Answer 3

Question

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

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Answer 4

Question

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

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Answer 5

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

Answer 6

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

Answer 7

Chapter 24, Problem 24.5YT

Interpretation Introduction

Interpretation:

s-cis conformation of the given diene is to be drawn.

Concept introduction:

The Diels–Alder reaction is a single step concerted reaction. The concerted nature of the Diels–Alder reaction means that both of the new carbon-carbon σ bonds form simultaneously. Thus, both ends of the diene must be relatively close to the dienophile in the transition state. The appropriate distances are achieved only if the diene attains a geometry in which the two ends of the π system are pointing in nearly the same direction, that is, s-cis conformation. The s indicates that the cis designation describes the orientation of groups about a single bond, rather than a double bond or the plane of a ring. Thus, for a Diels–Alder reaction to take place, the diene must be in the s-cis conformation.

Answer 8

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Answer 11

Ch. 24 - Prob. 24.1P Ch. 24 - Prob. 24.2P Ch. 24 - Prob. 24.3P Ch. 24 - Prob. 24.4P Ch. 24 - Prob. 24.5P Ch. 24 - Prob. 24.6P Ch. 24 - Prob. 24.7P Ch. 24 - Prob. 24.8P Ch. 24 - Prob. 24.9P Ch. 24 - Prob. 24.10P

Solution Summary: The author explains that the Diels–Alder reaction is a single step concerted reaction, where both of the new carbon-carbon bonds form simultaneously.

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Chapter 24 Solutions