The reaction involves ozonolysis of a cyclic alkene followed by reductive workup. The starting material appears to be a bicyclic compound with a double bond. Ozonolysis cleaves the double bond and forms carbonyl groups. The product A shown in option (B) is consistent with ozonolysis of a tetralin-like structure, forming an aldehyde on the ring. The correct answer is (B).
JEE Main · 2021 · 26 Feb 2021 · Shift 2 · Single correct option