ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
9th Edition
ISBN: 9780137249442
Author: Wade
Publisher: INTER PEAR
Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
These are in the wrong boxes.  Why does the one on the left have a lower molar mass than the one on the right?
SYNTHESIS REACTIONS. For the following reactions, synthesize the given products from the given reactants. Multiple reactions/steps will be needed. For the one of the steps (ie reactions) in each synthesis, write out the mechanism for that reaction and draw an energy diagram showing the correct number of hills and valleys for that step's mechanism. CI b. a. Use acetylene (ethyne) and any alkyl halide as your starting materials Br C. d. "OH OH III. OH
Calculate the pH and the pOH of each of the following solutions at 25 °C for which the substances ionize completely: (a) 0.200 M HCl

Chapter 19 Solutions

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS

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
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning