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Acetaldehyde $(CH_3CHO)$ reacts with:

An aromatic compound $A$ (Molecular formula $C_{8}H_{8}O$) gives a positive $2,4-DNP$ test. It gives a yellow precipitate of compound $B$ on treatment with iodine and sodium hydroxide solution. Compound $A$ does not give Tollen's or Fehling's test. On drastic oxidation with potassium permanganate,it forms a carboxylic acid $C$ (Molecular formula $C_{7}H_{6}O_{2}$),which is also formed along with the yellow compound in the above reaction. Identify $A, B$ and $C$ and write all the reactions involved.

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Acetone and acetaldehyde can be distinguished by

Which of the following aldehydes is less reactive towards nucleophilic addition reaction?

Identify the products of the following reaction:
$HCHO + C_6H_5CHO \xrightarrow[ii. \ H_3O^+]{i. \ conc. \ NaOH} ?$

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