Below is a reaction scheme for the transformation of 2-phenylethan-1-ol to the corresponding aldehyde. 요 S. H3C CH3 DMSO Oxalyl chloride PHCH,CH2OH DMSO = PHCH, `H EtzN Oxalyl chloride = .CI CI Draw a complete mechanism for the formation of the aldehyde from 2-phenylethan-1-ol using the reagents DMSO, oxalyl chloride and triethylamine. Ensure you show the formation of intermediate А. H3CCH3 А
Below is a reaction scheme for the transformation of 2-phenylethan-1-ol to the corresponding aldehyde. 요 S. H3C CH3 DMSO Oxalyl chloride PHCH,CH2OH DMSO = PHCH, `H EtzN Oxalyl chloride = .CI CI Draw a complete mechanism for the formation of the aldehyde from 2-phenylethan-1-ol using the reagents DMSO, oxalyl chloride and triethylamine. Ensure you show the formation of intermediate А. H3CCH3 А
Chemistry
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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
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:Below is a reaction scheme for the transformation of 2-phenylethan-1-ol to the corresponding
aldehyde.
DMSO
.S
Oxalyl chloride
H3C
CH3
PHCH,CH,OH
DMSO =
PHCH2
EtzN
Охаlyl chloride %3
CI
.CI
Draw a complete mechanism for the formation of the aldehyde from 2-phenylethan-1-ol using the
reagents DMSO, oxalyl chloride and triethylamine. Ensure you show the formation of intermediate
А.
H3C
CH3
A
0=
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