An organic compound (A) with molecular formula C$_3$H$_5$N on reaction with C$_6$H$_5$MgBr 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 C$_7$H$_6$O$_2$. Identify the compounds (A), (B) and (C). Write the reactions of compound (A) with C$_6$H$_5$MgBr followed by hydrolysis to give compound (B).