(a) Interpretation: The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated. Concept introduction: The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

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Answer 1

Question

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

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11:43 Q1. (a) (c) (d) (b) Two stereoisomers of but-2-ene are formed when 2-bromobutane reacts with ethanolic potassium hydroxide. (i) Explain what is meant by the term stereoisomers. Library Name and outline a mechanism for the reaction of 2-bromo-2-methylpropane with ethanolic potassium hydroxide to form the alkene 2-methylpropene, (CH3)2C=CH₂ Name of mechanism Mechanism (ii) Draw the structures and give the names of the two stereoisomers of but-2-ene. Stereoisomer 1 Name (iii) Name this type of stereoisomerism. Select Name Stereoisomer 2 When 2-bromo-2-methylpropane reacts with aqueous potassium hydroxide, 2-methylpropan-2-ol is formed as shown by the following equation. CH3 H₂C-C-CH3 + KOH Br Page 2 of 14 CH3 H3C-C-CH3 + KBr ОН State the role of the hydroxide ions in this reaction. Write an equation for the reaction that occurs when CH3CH₂CH₂CH₂Br reacts with an excess of ammonia. Name the organic product of this reaction. Equation Name of product 9,284 Photos, 1,166 Videos For You…

Answer 2

Question

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

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Answer 3

Question

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

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Answer 4

Question

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

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Answer 5

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Answer 6

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Answer 7

Chapter 11, Problem 11.7P

Interpretation Introduction

(a)

Interpretation:

The synthesis of dicyclohexyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The synthesis of tert-butyl-isobutyl ether using alkoxymercuration-reduction is to be stated.

Concept introduction:

The ethers are synthesized by the reaction of alkene with alcohol in presence of mercuric acetate. In the alkoxy mercuration reduction reaction, the alcohol acts as a nucleophile and reacts with mercurium ion intermediate.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 11 - Prob. 11.1P Ch. 11 - Prob. 11.2P Ch. 11 - Prob. 11.3P Ch. 11 - Prob. 11.4P Ch. 11 - Prob. 11.5P Ch. 11 - Prob. 11.6P Ch. 11 - Prob. 11.7P Ch. 11 - Prob. 11.8P Ch. 11 - Prob. 11.9P Ch. 11 - Prob. 11.10P

Solution Summary: The author explains the synthesis of dicyclohexyl ether using alkoxymercuration-reduction.

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