The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained. Concept introduction: In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons , the halogen atoms are attached to C-1 and C-4 carbon atoms respectively. In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

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Answer 1

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Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

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Answer 2

Question

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

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Answer 3

Question

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

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Answer 4

Question

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

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Answer 5

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

Answer 6

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

Answer 7

Chapter 12, Problem 46P

Interpretation Introduction

Interpretation:

The molecular structure of the product is to be drawn and with the help of resonating structure, the reason for the statement that addition is preferred to the central ring is to be explained.

Concept introduction:

In 1,4-addition halogenation reaction of polycyclic aromatic hydrocarbons, the halogen atoms are attached to C-1 and C-4 carbon atoms respectively.

In polycyclic aromatic hydrocarbons, the most stable resonance contributor is the one with the greatest number of rings that correspond to Kekule formulation of benzene.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 12.2 - Write structural formulas for toluene (C6H5CH3)...Ch. 12.3 - Prob. 2P Ch. 12.5 - Prob. 3P Ch. 12.5 - Prob. 4P Ch. 12.6 - Prob. 5P Ch. 12.6 - Chrysene is an aromatic hydrocarbon found in coal...Ch. 12.8 - Prob. 7P Ch. 12.9 - As measured by their first-order rate constants,...Ch. 12.9 - Give the structure of the principal organic...Ch. 12.9 - Prob. 10P

Solution Summary: The author explains the molecular structure of the product that would be formed if bromine adds to the central ring of anthracene.

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Chapter 12 Solutions