Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. 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 1 (Carbonyl compounds I) Explain how the class I carbonyl compound reacts? What will be the product when ethylamine and propyl amine reacts with acetyl chloride? Why only one amide obtained after the reaction of acetyl chloride with a mixture of ethylamine and trimethylamine? Excess amine is required in the reaction of acetyl chloride with amine whereas excess alcohol is not required in the reaction of acetyl chloride and alcohol. Why? List the following ester in order of decreasing reactivities towards hydrolysis with reason: Methyl benzoate, p-nitro methyl benzoate and p-methoxy methyl benzoate The reaction of an ester with an amine is not as slow as the reaction of an ester with water or an alcohol. Explain with reason. Explain why the rate of aminolysis of an ester cannot be increased by H+, OH- or OR-. How can you activate the carboxylic acid? Is acid catalyzed hydrolysis of acetamide a reversible or an irreversible reaction. Explain. Chapter 2 (Carbonyl compounds II)…
Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. c) m-bromoaniline

Chapter 19 Solutions

Organic Chemistry (9th Edition)

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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