The reason as to why phenyl tert- butyl sulfide canot be prepared by reaction of tert- butyl bromide with potassium benzenethiolate is to be stated. Concept introduction: Alkyl halides undergo elimination reaction in the presence of a base to form alkenes . The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Question

Want to see the full answer?

Answer 1

Question

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

ΗΝ, Draw Final Product C cyclohexanone pH 4-5 Edit Enamine H3O+ CH3CH2Br THF, reflux H Edit Iminium Ion

How many hydrogen atoms are connected to the indicated carbon atom?

Identify the compound with the longest carbon - nitrogen bond. O CH3CH2CH=NH O CH3CH2NH2 CH3CH2C=N CH3CH=NCH 3 The length of all the carbon-nitrogen bonds are the same

Answer 2

Question

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Answer 6

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Answer 7

Chapter 18, Problem 18.56AP

Interpretation Introduction

Interpretation:

The reason as to why phenyl tert-butyl sulfide canot be prepared by reaction of tert-butyl bromide with potassium benzenethiolate is to be stated.

Concept introduction:

Alkyl halides undergo elimination reaction in the presence of a base to form alkenes. The mechanism of the reaction depends on the base used. The most substituted alkene is formed as the major product according to Zaitsev rule.

Answer 8

Expert Solution & Answer

Answer 9

Expert Solution & Answer

Answer 10

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 11

Ch. 18 - Prob. 18.1P Ch. 18 - Prob. 18.2P Ch. 18 - Prob. 18.3P Ch. 18 - Prob. 18.4P Ch. 18 - Prob. 18.5P Ch. 18 - Prob. 18.6P Ch. 18 - Prob. 18.7P Ch. 18 - Prob. 18.8P Ch. 18 - Prob. 18.9P Ch. 18 - Prob. 18.10P

Solution Summary: The author explains that tert-butyl bromide and potassium benzenethiolate undergo elimination reactions to form alkenes.

Want to see the full answer?

Chapter 18 Solutions