The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained. Concept introduction: Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction . In β-Elimination reaction, elimination of one proton and one halo group is taking place. The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes . To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

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Answer 1

Question

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

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Answer 2

Question

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

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Answer 3

Question

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

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Answer 4

Question

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

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Answer 5

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

Answer 6

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

Answer 7

Chapter 8, Problem 60PP

Interpretation Introduction

Interpretation:

The product formed after treating 3-bromo-2, 4-dimethylpentane with sodium hydroxide has to be drawn and the reason for only one regiochemical outcome of the given reaction is to be explained.

Concept introduction:

Alkenes are formed when alkyl halides are treated with bases via β-elimination reaction. In β-Elimination reaction, elimination of one proton and one halo group is taking place.

The product of the elimination reaction is depends upon the two 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 this type of reaction is called regioselective and the products are called as regiochemical outcomes.

To draw: the products of the given reaction and explain the reason for only one regiochemical outcome for this reaction.

Answer 8

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Answer 9

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Answer 10

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Answer 11

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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