Question

An organic compound with molecular formula c9 h10 forms 2 4 dnp derivative reducing tollens reagent in under undergo cannizzaro reaction on vigorous oxidation it gives 12 benzene dye carbon to carboxylic acid identify the compound

Answer 1

Answer:

(CH3CO)'2

Explanation:

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Answer 2

$\huge\textcolor{orange}{\texttt{Answer :-}}$

The given compound forms 2,4-DNP derivative. Therefore, it is an aldehyde or ketone. Since it reduces Tollen's reagent, it must be an aldehyde. The compound undergoes Cannizzaro's reaction, so it does not contain $\alpha-$hydrogen.

On vigorous oxidation, it gives 1,2-benzendicarboxylic acid, it means that it must be containing an alkyl group at 2-position with respect to —CHO group on the benzene ring.