ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Question
Chapter 5, Problem 56P
(a)
Interpretation Introduction
Interpretation: The structure of the enantiomer of the arabinose needs to be drawn.
Concept Introduction: Enantiomer has an opposite configuration about the chiral atom.
(b)
Interpretation Introduction
Interpretation: The other enantiomer needs to be drawn.
Concept Introduction: Enantiomer has just opposite configuration about the chiral atom.
(c)
Interpretation Introduction
Interpretation: The structure of diastereomer of arabinose needs to be determined.
Concept Introduction:Diastereomer has the same configuration but opposite configuration about chiral atom.
(d)
Interpretation Introduction
Interpretation: The number of other diastereomer needs to be determined.
Concept Introduction:Diastereomer has just opposite configuration about chiral atom, rest configuration will be same.
(e)
Interpretation Introduction
Interpretation:The rotation of the structure needs to be determined.
Concept Introduction:Rotation is defined as an angle how much the group is rotated about chiral atom of the molecule.
(f)
Interpretation Introduction
Interpretation: The rotation of diastereomer needs to be determined.
Concept Introduction:Diastereomer has rotation about chiral atom only.
(g)
Interpretation Introduction
Interpretation: The optically inactive diastereomer needs to be explained.
Concept Introduction:If a diastereomer has a plane of mirror then it is optically inactive.
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Students have asked these similar questions
Indicate the substitutes in one place, if they are a diazonio room.
Indicate the product formed in each reaction. If the
product exhibits tautomerism, draw the tautomeric
structure.
a) о
+ CH3-NH-NH2
CO2C2H5
b)
+ CoH5-NH-NH2
OC2H5
Indicate the formula of the compound, that is the result of the N-
alquilación (nucleofílic substitution), in which an additional lateral
chain was formed (NH-CH2-COOMe).
F3C.
CF3
NH
NH2
Br о
OMe
K2CO3, DABCO, DMF
Chapter 5 Solutions
ORGANIC CHEMISTRY (LL)-PACKAGE
Ch. 5.1 - Prob. 5.3ECh. 5.1 - Prob. 5.4ECh. 5.1 - Prob. 5.5ECh. 5.2 - Prob. 5.6ECh. 5.2 - Prob. 5.8TIYCh. 5.3 - Prob. 5.9ECh. 5.3 - Prob. 5.11TIYCh. 5.3 - Prob. 5.12ECh. 5.4 - Prob. 5.13ECh. 5.4 - Prob. 5.14E
Ch. 5.4 - Prob. 5.16TIYCh. 5.4 - Prob. 5.17ECh. 5.5 - Prob. 5.18ECh. 5.5 - Prob. 5.19ECh. 5.5 - Prob. 5.20ECh. 5.6 - Prob. 5.21ECh. 5.6 - Prob. 5.22ECh. 5.6 - Prob. 5.23ECh. 5.7 - Prob. 5.24ECh. 5.7 - Prob. 5.26TIYCh. 5.7 - Prob. 5.27ECh. 5 - Prob. 5.1ECh. 5 - Prob. 5.2ECh. 5 - Prob. 30PCh. 5 - Prob. 31PCh. 5 - Prob. 32PCh. 5 - Prob. 33PCh. 5 - Prob. 34PCh. 5 - Prob. 35PCh. 5 - Prob. 36PCh. 5 - Prob. 37PCh. 5 - Prob. 38PCh. 5 - Prob. 39PCh. 5 - Prob. 40PCh. 5 - Prob. 41PCh. 5 - Prob. 42PCh. 5 - Prob. 43PCh. 5 - Prob. 44PCh. 5 - Prob. 45PCh. 5 - Prob. 46PCh. 5 - Prob. 47PCh. 5 - Prob. 48PCh. 5 - Prob. 49PCh. 5 - Prob. 50PCh. 5 - Prob. 51PCh. 5 - Prob. 52PCh. 5 - Prob. 53PCh. 5 - Prob. 54PCh. 5 - Prob. 55PCh. 5 - Prob. 56PCh. 5 - Prob. 57PCh. 5 - Prob. 58PCh. 5 - Prob. 59PCh. 5 - Prob. 60PCh. 5 - Prob. 61PCh. 5 - Prob. 62PCh. 5 - Prob. 63PCh. 5 - Prob. 64PCh. 5 - Prob. 65PCh. 5 - Prob. 66PCh. 5 - Prob. 67PCh. 5 - Prob. 68PCh. 5 - Prob. 69PCh. 5 - Prob. 70PCh. 5 - Prob. 71P
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