Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Question
Chapter 17, Problem 54P
Interpretation Introduction
Interpretation:
The structures of the compounds A-D in the given reaction for the synthesis of ibuprofen is to be supplied.
Concept introduction:
Ibuprofen is an anti-inflammatory agent. The formation of ibuprofen is based on only the (S) isomer.
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C) a nitrile
D) an amine nitrite salt
DIRECTIONS: Each of the following questions
or incomplete statements below is followed by four
suggested answers lettered A - D. Select or
choose the letters of the best answer to the
question or incomplete statement.
7. An organic nitrogen compound, X, gives
ammonia on warming with dilute aqueous
sodium hydroxide, X could be
A) ethanamide B) ethylamine
C) phenylamine D) amino ethanoic acid
Which one of the following reagents reacts
1.
in a similar fashion with both phenylamine
(C H,NH,) and ethylamine.
A) Br,(aq)
C) conc. HNO, D) cold HNO (aq)
2. Phenylamine (aniline) can be prepared by
reducing nitrobenzene with tin and
concerntrated hydrochloric acid followed by
the addition of alkali and finally steam
distillation. The alkali is added to;
A) prevent oxidation of phenylamine.
B) liberate free phenylamine from solution
C) dissolve excess nitro benzene
D) dissolve the phenylamine
8. Arrange the following molecules in their
increasing order of base…
Nn.11.
Subject:- Chemistry
A postgraduate student wanted to synthesized two carbonyl compounds known as compounds M and N using oxidation of alcohol. However, these carbonyl compounds should have more than 6 carbon atoms
Draw two (2) possible structural formulae for compounds M and N.
How would you distinguish between M and N?
Chapter 17 Solutions
Organic Chemistry
Ch. 17 - Practice Problem 17.1 Give an IUPAC systematic...Ch. 17 - Prob. 2PPCh. 17 - Practice Problem 17.3 Write structural formulas...Ch. 17 - Practice Problem 17.4
Show how each of the...Ch. 17 - Practice Problem 17.5
Show how you could prepare...Ch. 17 - Practice Problem 17.6
(a) Which of the carboxylic...Ch. 17 - Prob. 7PPCh. 17 - Prob. 8PPCh. 17 - Practice Problem 17.9
Esters can also be...Ch. 17 - Prob. 10PP
Ch. 17 - Prob. 11PPCh. 17 - Practice Problem 17.12
What products would you...Ch. 17 - Practice Problem 17.13 (a) Provide the reagents...Ch. 17 - Prob. 14PPCh. 17 - Practice Problem 17.15 Using decarboxylation...Ch. 17 - Practice Problem 17.16 Diacyl peroxides, ,...Ch. 17 - Prob. 17PCh. 17 - Give an IUPAC systematic or common name for each...Ch. 17 - Prob. 19PCh. 17 - Prob. 20PCh. 17 - 17.21 What major organic product would you expect...Ch. 17 - Prob. 22PCh. 17 - Prob. 23PCh. 17 - Prob. 24PCh. 17 - Prob. 25PCh. 17 - 17.26 What products would you expect to obtain...Ch. 17 - Write structural formulas for the major organic...Ch. 17 - 17.28 Indicate reagents that would accomplish each...Ch. 17 - Write structural formulas for the major organic...Ch. 17 - Prob. 30PCh. 17 - Prob. 31PCh. 17 - Prob. 32PCh. 17 - 17.33 On heating,...Ch. 17 - Prob. 34PCh. 17 - Prob. 35PCh. 17 - 17.36 Show how pentanoic acid can be prepared from...Ch. 17 - 17.37 The active ingredient of the insect...Ch. 17 - Prob. 38PCh. 17 - Prob. 39PCh. 17 - Give stereochemical formulas for compounds AQ:...Ch. 17 - 17.41 -Glyceraldehyde can be transformed into...Ch. 17 - Prob. 42PCh. 17 - Prob. 43PCh. 17 - 17.44 Given here are the NMR spectra and carbonyl...Ch. 17 - 17.45 Compound Y dissolves slowly when warmed...Ch. 17 - Prob. 46PCh. 17 - Prob. 47PCh. 17 - Prob. 48PCh. 17 - Prob. 49PCh. 17 - Prob. 50PCh. 17 - Prob. 51PCh. 17 - 17.52 Starting with 1-naphthol, suggest an...Ch. 17 - Suggest a synthesis of ibuprofen (Section 5.11)...Ch. 17 - Prob. 54PCh. 17 - Prob. 55PCh. 17 - Prob. 1LGPCh. 17 - Prob. 2LGPCh. 17 - Prob. 3LGPCh. 17 - Prob. 4LGP
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