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ORGANIC CHEMISTRY-ETEXT REG ACCESS
12th Edition
ISBN: 9781119308362
Author: Solomons
Publisher: WILEY
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Chapter H, Problem 2PP
Interpretation Introduction
Interpretation:
The chirality centre in hyoscyamine involved in the racemization and the three dimensional structure of hyoscyamine is to be written.
Concept introduction:
▸ The chemical formula of atropine is
▸ On hydrolysis of atropine, tropine and tropic acid are formed, which indicates that it is an ester.
▸ It is optically inactive. Atropine is a racemate form of hyoscyamine. It is insoluble in ether but easily soluble in chloroform and alcohol and also sparingly soluble in water.
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Students have asked these similar questions
3) Stereoisomers differ from each other in what respect?
A) composition
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C) configuration
D) steric hindrance
E) none of the above
3) Which of the following molecules are enantiomers
Он
OH
OH
"NH2
'NH2
H2N
ČI
(a)
(b)
(c)
CI
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Following are four Newman projection formulas for tartaric add.
(a) Which represent the same compound?
(b) Which represent enantiomers?
(c) Which represent a meso compund?
(d) What are diastereomers?
Chapter H Solutions
ORGANIC CHEMISTRY-ETEXT REG ACCESS
Ch. H - Prob. 1PPCh. H - Prob. 2PPCh. H - Prob. 3PPCh. H - Practice Problem H.4
In 1891 G. Merling...Ch. H - Practice Problem H.5
Many alkaloids appear to be...Ch. H - Practice Problem H.6 Papaverine has been...Ch. H - Practice Problem H.7
One of the important steps in...Ch. H - Prob. 8PPCh. H - Practice Problem H.9 Gramine has been synthesized...
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