To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH 3 ) 2 CCH 2 + Concept introduction: Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

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Answer 1

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Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

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Answer 2

Question

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

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Answer 3

Question

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

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Answer 4

Question

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

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Answer 5

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

Answer 6

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

Answer 7

Chapter D, Problem D.1YT

Interpretation Introduction

Interpretation:

To draw the diagram to show hyperconjugation in 2, 2-dimethylpropyl cation (CH₃)₂CCH₂⁺

Concept introduction:

Stability of carbocations can be explained on the basis of inductive effect and hyperconjugation. Hyperconjugation has a major contribution. Constructive interference produces an orbital more stable than the sigma bonding orbital while destructive interference results in a less stable orbital.

Answer 8

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Answer 11

Ch. D - Prob. D.1P Ch. D - Prob. D.2P Ch. D - Prob. D.3P Ch. D - Prob. D.4P Ch. D - Prob. D.5P Ch. D - Prob. D.6P Ch. D - Prob. D.7P Ch. D - Prob. D.8P Ch. D - Prob. D.9P Ch. D - Prob. D.10P

Solution Summary: The author explains that hyperconjugation enhances the stability of (CH 3 ) 2 CCH 2 +

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