From the electrostatic potential map of (trifluoromethyl) benzene, C 6 H 5 CF 3 , whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained. Concept introduction: In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green. In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene. To state and explain: From the electrostatic potential map of (trifluoromethyl) benzene, C 6 H 5 CF 3 , whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

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Answer 1

Question

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

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Provide the missing information. *see image

Answer 2

Question

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

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Answer 3

Question

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

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Answer 4

Question

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

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Answer 5

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

Answer 6

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

Answer 7

Chapter 16.4, Problem 11P

Interpretation Introduction

Interpretation:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution is to be stated and explained.

Concept introduction:

In the electrostatic potential map the electron rich regions are indicated in red and electron poor regions are indicated in green.

In aromatic electrophilic substitution reactions of the monosubstituted benzenes, if the group already present is electron releasing it will activate the ring and hence the monosubstituted benzene will be more reactive than benzene. If it is electron withdrawing it will deactivate the ring and hence the monosubstituted benzene will be less reactive than benzene.

To state and explain:

From the electrostatic potential map of (trifluoromethyl) benzene, C₆H₅CF₃, whether it will be more reactive or less reactive than toluene towards electrophilic substitution.

Answer 8

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Answer 19

Ch. 16.1 - Prob. 1P Ch. 16.2 - Propose a mechanism for the electrophilic...Ch. 16.2 - How many products might be formed on chlorination...Ch. 16.2 - When benzene is treated with D2SÅª4. deuterium...Ch. 16.3 - Prob. 5P Ch. 16.3 - What is the major monosubstitution product from...Ch. 16.3 - Identify the carboxylic acid chloride that might...Ch. 16.4 - Rank the compounds in each of the following groups...Ch. 16.4 - Predict the major products of the following...Ch. 16.4 - Prob. 10P

Solution Summary: The author analyzes the electrostatic potential map of (trifluoromethyl) benzene, C 6 H 5 CF 3.

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