EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
6th Edition
ISBN: 8220103151757
Author: LOUDON
Publisher: MAC HIGHER
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Chapter 16, Problem 16.62AP
Interpretation Introduction

(a)

Interpretation:

Whether 1-methoxynapthalene nitrates more rapidly or more slowly than naphthalene at carbon -4 is to be stated. The reason for this is to be explained.

Concept introduction:

Nitration is a process in which an aromatic compound is nitrated by electrophilic substitution mechanism in presence of concentrated sulfuric acid and concentrated nitric acid. Electron donating groups substituted on the aromatic ring are those which donates electron to the aromatic ring. Electron donating groups are ortho and para-directing.

Interpretation Introduction

(b)

Interpretation:

Whether 1-methoxynapthalene nitrates more rapidly or more slowly than naphthalene at carbon -5 is to be stated. The reason for this is to be explained.

Concept introduction:

Nitration is a process in which an aromatic compound is nitrated by electrophilic substitution mechanism in presence of concentrated sulfuric acid and concentrated nitric acid. Electron donating groups substituted on the aromatic ring are those which donates electron to the aromatic ring. Electron donating groups are ortho and para-directing.

Interpretation Introduction

(c)

Interpretation:

Whether 1-methoxynapthalene nitrates more rapidly or more slowly than naphthalene at carbon -6 is to be stated. The reason for this is to be explained.

Concept introduction:

Nitration is a process in which an aromatic compound is nitrated by electrophilic substitution mechanism in presence of concentrated sulfuric acid and concentrated nitric acid. Electron donating groups substituted on the aromatic ring are those which donates electron to the aromatic ring. Electron donating groups are ortho and para-directing.

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Chapter 16 Solutions

EBK ORGANIC CHEMISTRY

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