(a) Interpretation: For the given substrate, when NaOH is used as the base, the major E2 product is to be drawn. Concept introduction: In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene . The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

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Answer 1

Question

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

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Answer 2

Question

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

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Answer 3

Question

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

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Answer 4

Question

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

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Answer 5

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 6

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Answer 7

Chapter 9, Problem 9.68P

Interpretation Introduction

(a)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms.

Answer 8

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 9

Interpretation Introduction

(b)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 10

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 11

Interpretation Introduction

(c)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 12

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 13

Interpretation Introduction

(d)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 14

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 15

Interpretation Introduction

(e)

Interpretation:

For the given substrate, when $NaOH$ is used as the base, the major E2 product is to be drawn.

Concept introduction:

In an E2 reaction, the base pulls off the proton from the substrate, thus forcing the leaving group to leave. Elimination usually takes place so as to produce the most stable, meaning highly alkyl substituted, alkene. The major elimination product is the one produced by deprotonating the carbon atom initially attached to the fewest hydrogen atoms. In a ring with limited rotation, the leaving group has to be trans to the proton.

Answer 16

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Answer 17

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Answer 18

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Answer 19

Ch. 9 - Prob. 9.1P Ch. 9 - Prob. 9.2P Ch. 9 - Prob. 9.3P Ch. 9 - Prob. 9.4P Ch. 9 - Prob. 9.5P Ch. 9 - Prob. 9.6P Ch. 9 - Prob. 9.7P Ch. 9 - Prob. 9.8P Ch. 9 - Prob. 9.9P Ch. 9 - Prob. 9.10P

Solution Summary: The author explains the structure of the major E2 product for the given substrate. Elimination takes place so as to produce the most stable, meaning highly alkyl substituted, alkene.

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Chapter 9 Solutions