For the given compounds, the most stable compound should be identified. Concept introduction: The compounds having two C = C π bonds are called dienes . Based on the proximity of C = C bonds in dienes, they are classified into three. Cumulated dienes: the C = C bonds are located adjacent carbons. Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond. Isolated dienes: the C = C bonds are separated by two or more σ-bonds. The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

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Answer 1

Question

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

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Answer 2

Question

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

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Answer 3

Question

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

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Answer 4

Question

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

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Answer 5

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

Answer 6

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

Answer 7

Chapter 17.2, Problem 5CC

Interpretation Introduction

Interpretation:

For the given compounds, the most stable compound should be identified.

Concept introduction:

The compounds having two C = C π bonds are called dienes.

Based on the proximity of C = C bonds in dienes, they are classified into three.

Cumulated dienes: the C = C bonds are located adjacent carbons.

Conjugated dienes: the C = C bonds or C = C and C = O are separated by one σ-bond.

Isolated dienes: the C = C bonds are separated by two or more σ-bonds.

The conjugated dienes are more stable as compare to isolated dienes because the delocalization of π bonds is taking place, so this forms some stabilization energy in conjugated system.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 17.1 - Prob. 1CC Ch. 17.2 - Prob. 2CC Ch. 17.2 - Prob. 3CC Ch. 17.2 - Prob. 4CC Ch. 17.2 - Prob. 5CC Ch. 17.3 - Prob. 6CC Ch. 17.4 - Prob. 1LTS Ch. 17.4 - Prob. 7PTS Ch. 17.4 - Prob. 8ATS Ch. 17.4 - Prob. 9ATS

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