Uploaded March 2021 | Updated September 2026, 1 week ago
The mechanism for the oxidation of an alcohol to a ketone using chromic acid. In order for a ketone to be produced, the starting alcohol must be a secondary alcohol. Notice that multiple water molecules are used in the mechanism, however it is only shown that one water molecule is produced from protonation with the chromic acid. It is likely though that the chromic acid as well as acid catalyst are in enough excess that multiple water molecules will be produced that can be used within the mechanism.
Music by Ryan Little - Arena - thmatc.co/?l=34C2596E
The mechanism for the oxidation of an alcohol to a ketone using chromic acid. In order for a ketone to be produced, the starting alcohol must be a secondary alcohol. Notice that multiple water molecules are used in the mechanism, however it is only shown that one water molecule is produced from protonation with the chromic acid. It is likely though that the chromic acid as well as acid catalyst are in enough excess that multiple water molecules will be produced that can be used within the mechanism.
Music by Ryan Little - Arena - thmatc.co/?l=34C2596E










