1.

Is it possible to oxidise t-butyl alcohol using acidified dichromate to form a carbonyl compound.

Answer»

SOLUTION :`3^(@)`-alcohols do not undergo oxidation reaction under normal condition, but at elevated temperature, under strong oxidising agent CLEAVAGE of C - C bond takes place to give a mixture of carboxylic acid.
Yes, it is possible. `t` - butyl alcohol is readily oxidising in ACIDIC solution `(K_(2)Cr_(2)O_(7)//H_(2)SO_(4))` to a mixture of a KETONE and an acid each containing lesser number of carbon atoms than the original alcohol. The oxidation presumably occur via alkenes formed through dehydration of alcohols uder acidic conditions.


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