For the each given descriptions the used compound are needed to be drawn. Concept introduction: In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons. The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical . If the β-positions are different and the products formed are also different . This means the double bond can form in two different regions, so it will give different alkene products. If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible. To draw: the alkyl halide fitted for given descriptions.

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Answer 1

Question

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

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Answer 2

Question

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

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Answer 3

Question

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

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Answer 4

Question

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

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Check out a sample textbook solution

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Answer 5

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 6

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 7

Chapter 8, Problem 65PP

(a)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 8

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 9

(b)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 10

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 11

(c)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 12

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 13

(d)

Interpretation Introduction

Interpretation:

For the each given descriptions the used compound are needed to be drawn.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one β-proton and one α-halo group of the alkyl halide. The double bond is located between α,β-carbons.

The product of the elimination reaction is depends upon the β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions, so it will give different alkene products.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity, cis,tran-sisomers are possible.

To draw: the alkyl halide fitted for given descriptions.

Answer 14

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Answer 15

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Answer 16

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Answer 17

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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