[Solution from source] With FeCl₃ (Lewis acid) chlorine substitutes the ring at the o- and p-positions activated by CH₃, giving o- and p-chlorotoluene (X). In light, free-radical substitution occurs on the side chain; with excess Cl₂ this goes to C₆H₅CCl₃, trichloromethylbenzene (Y). Benzyl chloride is a side-chain product, so it cannot be X. Answer (4).