Elimination approach: Benzoic acid would need oxidation of a side chain, which isn't happening here. Plain benzene would mean losing the hydroxyl group entirely, which this reaction doesn't do. Anisole would require methylation, but there's no methylating agent present. What actually happens is the phenoxide ion attacking carbon dioxide next to the oxygen, the Kolbe-Schmitt carboxylation, and acidifying the resulting salt frees salicylic acid, option (B).