Can you show the mechanism and do you any rules that will allow you to determine the answer without the mechanism? And any other information. How to do it? Can you explain it?

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
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Can you show the mechanism and do you any rules that will allow you to determine the answer without the mechanism? And any other information. How to do it? Can you explain it?

 

Chromic acid oxidation of primary alcohols to aldehydes which
then easily oxidize to carboxylic acids.
R-CH₂OH +
1° alcohol
H
R-C=0 + HCrO3
Aldehyde Chromium IV
H3O+
H
R-COH
ОН
protonated
aldehyde
O
0
+6
Cr
5=0
H₂O
then -H
HCrO3 + H3O+
Chromium IV
E-2 elimination
H₂O:
(a base)
+
+
-R-CH₂O
H
R-C-OH
OH
:
0: O-I
H-C
R-O
Н
-I
O
HO
A geminal diol
H₂O:
Cr
+6/
5=0
0=0=0
R-CO
Carboxylic acid
Cr
proton transfer
A chromate ester
intermediate
DO
O Cr-OH
0=0=0
O
OH
R-COC OH
H
0=0=0
Cr
Transcribed Image Text:Chromic acid oxidation of primary alcohols to aldehydes which then easily oxidize to carboxylic acids. R-CH₂OH + 1° alcohol H R-C=0 + HCrO3 Aldehyde Chromium IV H3O+ H R-COH ОН protonated aldehyde O 0 +6 Cr 5=0 H₂O then -H HCrO3 + H3O+ Chromium IV E-2 elimination H₂O: (a base) + + -R-CH₂O H R-C-OH OH : 0: O-I H-C R-O Н -I O HO A geminal diol H₂O: Cr +6/ 5=0 0=0=0 R-CO Carboxylic acid Cr proton transfer A chromate ester intermediate DO O Cr-OH 0=0=0 O OH R-COC OH H 0=0=0 Cr
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