Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
9th Edition
ISBN: 9780135213728
Author: Leroy Wade, Jan Simek
Publisher: PEARSON+
Question
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Chapter 19.20C, Problem 19.31P

(a)

Interpretation Introduction

To show: The preparation of aniline by aromatic nitration, followed by reduction.

Interpretation: The preparation of aniline by aromatic nitration, followed by reduction is to be shown.

Concept introduction: Aniline is an aromatic compound with the formula C6H5NH2. Aromatic nitration process involves the introduction of nitro group in the aromatic ring. In the process of nitration a mixture of concentrated sulphuric acid and nitric acid involves. This mixture gives nitronium ion which is an active species for the process of nitration.

(b)

Interpretation Introduction

To show: The preparation of p-bromoaniline by aromatic nitration, followed by reduction.

Interpretation: The preparation of p-bromoaniline by aromatic nitration, followed by reduction is to be shown.

Concept introduction: Para-bromoaniline is an aromatic compound with the formula C6H4NH2Br. Aromatic nitration process involves the introduction of nitro group in the aromatic ring. In the process of nitration a mixture of concentrated sulphuric acid and nitric acid involves. This mixture gives nitronium ion which is an active species for the process of nitration.

(c)

Interpretation Introduction

To show: The preparation of m-bromoaniline by aromatic nitration, followed by reduction.

Interpretation: The preparation of m-bromoaniline by aromatic nitration, followed by reduction is to be shown.

Concept introduction: Mata-bromoaniline is an aromatic compound with the formula C6H4NH2Br. Aromatic nitration process involves the introduction of nitro group in the aromatic ring. In the process of nitration a mixture of concentrated sulphuric acid and nitric acid involves. This mixture gives nitronium ion which is an active species for the process of nitration.

(d)

Interpretation Introduction

To show: The preparation of m-aminobenzoic acid by aromatic nitration, followed by reduction.

Interpretation: The preparation of m-aminobenzoic acid by aromatic nitration, followed by reduction is to be shown.

Concept introduction: m-aminobenzoic is an aromatic compound with the formula C6H4NH2COOH. Aromatic nitration process involves the introduction of nitro group in the aromatic ring. In the process of nitration a mixture of concentrated sulphuric acid and nitric acid involves. This mixture gives nitronium ion which is an active species for the process of nitration.

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Chapter 19 Solutions

Pearson eText Organic Chemistry -- Instant Access (Pearson+)

Ch. 19.10B - Propose a mechanism for nitration of pyridine at...Ch. 19.10B - Prob. 19.12PCh. 19.10C - Prob. 19.13PCh. 19.10C - Prob. 19.14PCh. 19.11 - Propose a mechanism to show the individual...Ch. 19.11 - Prob. 19.16PCh. 19.12 - Give the products expected from the following...Ch. 19.13 - Prob. 19.18PCh. 19.13 - Prob. 19.19PCh. 19.14 - Prob. 19.20PCh. 19.15 - Prob. 19.21PCh. 19.15 - Prob. 19.22PCh. 19.16 - Prob. 19.23PCh. 19.17 - Prob. 19.24PCh. 19.17 - Prob. 19.25PCh. 19.18 - Prob. 19.26PCh. 19.19 - Prob. 19.27PCh. 19.20A - Addition of one equivalent of ammonia to...Ch. 19.20A - Prob. 19.29PCh. 19.20B - Show how you would accomplish the following...Ch. 19.20C - Prob. 19.31PCh. 19 - For each compound, 1. classify the...Ch. 19 - Prob. 19.33SPCh. 19 - Within each structure, rank the indicated...Ch. 19 - In each pair of compounds, select the stronger...Ch. 19 - Which of the following compounds are capable of...Ch. 19 - Complete the following proposed acid-base...Ch. 19 - Predict the products of the following reactions:...Ch. 19 - Prob. 19.39SPCh. 19 - Show how m-toluidine can be converted to the...Ch. 19 - The mass spectrum of tert-butylamine follows shows...Ch. 19 - Prob. 19.42SPCh. 19 - The following drugs are synthesized using the...Ch. 19 - Prob. 19.44SPCh. 19 - Synthesize from benzene. (Hint: All of these...Ch. 19 - Propose mechanisms for the following reactions.Ch. 19 - Prob. 19.47SPCh. 19 - Prob. 19.48SPCh. 19 - Prob. 19.49SPCh. 19 - Show how you can synthesize the following...Ch. 19 - Prob. 19.51SPCh. 19 - The alkaloid coniine has been isolated from...Ch. 19 - A chemist is summoned to an abandoned...Ch. 19 - Pyrrole undergoes electrophilic aromatic...Ch. 19 - Prob. 19.55SPCh. 19 - Prob. 19.56SPCh. 19 - An unknown compound shows a weak molecular ion at...Ch. 19 - A compound of formula C11H16N2 gives the IR,...Ch. 19 - (A true story.) A drug user responded to an ad...Ch. 19 - Prob. 19.60SPCh. 19 - Prob. 19.61SPCh. 19 - Prob. 19.62SPCh. 19 - Prob. 19.63SPCh. 19 - Prob. 19.64SPCh. 19 - Prob. 19.65SP
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