An organic compound (A) with molecular formula $\mathrm{C_3H_5N}$ on reaction with $\mathrm{C_6H_5MgBr}$ followed by hydrolysis, gives a compound (B). Compound (B) forms an orange-red precipitate with 2,4-DNP reagent and does not give iodoform test. It neither reduces Tollens' or Fehling's reagent nor does it decolourise bromine water. On drastic oxidation with chromic acid it gives a carboxylic acid (C) having molecular formula $\mathrm{C_7H_6O_2}$. Identify the compounds (A), (B) and (C). Write the reactions of compound (A) with $\mathrm{C_6H_5MgBr}$ followed by hydrolysis to give compound (B).