2. Provide the major product(s) for the reactions below. Clearly indicate the stereochemistry in your structureswhere appropriate. Where more than one stereoisomer is formed you only need to draw one of thestereoisomeric products. Other stereoisomers should be indicated by writing, "+enantiomer" or"+diastereomer", as appropriate. Check the boxes on the right to indicate whether the reaction product solutionwould be optically active ([a]o #0) or not optically active ([a] = 0). Under the checkboxes give your rationale forthe selection using one of the following: achiral, racemic, meso, single enantiomer, mixture of diastereomers.c)d)CICIBrCH3OHNaCNDMSOKBrDMFCH CH2OH[a]D#0 [a]D=0[a] #0 [a] = 0[a] #0 [a]D=0[a]D#0 [a]D=0

Substitution reactions are reactions in which the leaving group is replaced by a nucleophile. These…

Answered: a) b) c) CI Br CH₂OH NaCN DMSO KBr DMF

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a) b) c) CI Br CH₂OH NaCN DMSO KBr DMF

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

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Question

2. Provide the major product(s) for the reactions below. Clearly indicate the stereochemistry in your structures
where appropriate. Where more than one stereoisomer is formed you only need to draw one of the
stereoisomeric products. Other stereoisomers should be indicated by writing, "+enantiomer" or
"+diastereomer", as appropriate. Check the boxes on the right to indicate whether the reaction product solution
would be optically active ([a]o #0) or not optically active ([a] = 0). Under the checkboxes give your rationale for
the selection using one of the following: achiral, racemic, meso, single enantiomer, mixture of diastereomers.
c)
d)
CI
CI
Br
CH3OH
NaCN
DMSO
KBr
DMF
CH CH2OH
[a]D#0 [a]D=0
[a] #0 [a] = 0
[a] #0 [a]D=0
[a]D#0 [a]D=0

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