The mechanism for the preparation of 1-phenylcyclohexene from the reaction of benzene and cyclohexene is to be explained. Concept introduction: The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction. The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds . The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation. The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Question

Want to see the full answer?

Answer 1

Question

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Illustrate reaction mechanisms of alkenes with water in the presence of H2SO4, detailing each step of the process. Please show steps of processing. Please do both, I will thumb up for sure #1 #3

Draw the following molecule: (Z)-1-chloro-1-butene

Identify the molecule as having a(n) E, Z, cis, or trans configuration. CH3 H₁₂C ○ E ○ z ○ cis trans

Answer 2

Question

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Answer 6

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

Answer 7

Chapter 13.6, Problem 9P

Interpretation Introduction

Interpretation:

The mechanism for the preparation of 1-phenylcyclohexene from the reaction of

benzene and cyclohexene is to be explained.

Concept introduction:

The reaction that involves the substitution of aromatic ring by alkyl group is called alkylation reaction.

The alkyl halide or the compound that forms stable carbocation can also be used for the alkylation of aromatic compounds.

The π electrons of benzene attack the carbocation and cause it to undergo substitution followed by deprotonation of cyclohexadienyl cation.

The double bond at benzylic position can be introduced by the benzylic bromination with N-bromosuccinimide (NBS) followed by dehydrohalogenation.

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. 13.2 - Based on Hammonds postulate which holds that the...Ch. 13.3 - Prob. 2P Ch. 13.3 - Using : O =N+= O : as the electrophile, write a...Ch. 13.4 - Prob. 4P Ch. 13.5 - Prob. 5P Ch. 13.6 - Prob. 6P Ch. 13.6 - Write a reasonable mechanism for the formation of...Ch. 13.6 - tert-Butylbenzene can be prepared by alkylation of...Ch. 13.6 - Prob. 9P Ch. 13.7 - The reaction shown gives a single product in 88...

Solution Summary: The author explains the mechanism for the preparation of 1-phenylcyclohexene from the reaction of benzen

Want to see the full answer?

Chapter 13 Solutions