An aromatic hydrocarbons A reacts with propene in the presence of anhydrous AlCl_(3) to give a compound B with a molecular formula C_(9)H_(12). Further compound B undergoes oxidation in the, presence of air to give hydrogenperoxide C. Compound C decomposes in HCl acid solutions to give compound D and acetone. Identify A,B, C and D. Explain the reactions.

An aromatic hydrocarbons A reacts with propene in the presence of anhy

1.	An aromatic hydrocarbons A reacts with propene in the presence of anhydrous AlCl_(3) to give a compound B with a molecular formula C_(9)H_(12). Further compound B undergoes oxidation in the, presence of air to give hydrogenperoxide C. Compound C decomposes in HCl acid solutions to give compound D and acetone. Identify A,B, C and D. Explain the reactions.
Answer» Solution :(i) An aromatic hydrocarbon A reacts with propene in the presence of anhydrous `AlCl_(3)` to give COMPOUND B. (II) Compound B undergoes OXIDATION in the presence of air and hydrogenperoxide to give C. (iii) Compound C decomposes in HCl ACID solution to give compound D and acetone. Identify A, B, C and D. Explain the reactions.