In an experimental setup, a novel organic compound, L, with a molecular formula C7H8O2, is synthesized. This compound exhibits unique reactivity patterns: it forms a pink complex with FeCl3 solution, suggesting phenolic OH groups, and it gives a positive iodoform test, indicative of a methyl ketone group. Additionally, L does not decolorize bromine water, implying it does not have carbon-carbon double bonds. Based on these observations and the principles of organic chemistry, what is the most likely structure for compound L? Options: a) 4-hydroxyacetophenone b) 2-hydroxybenzoic acid (salicylic acid) c) 3-hydroxybenzaldehyde d) 1,4-dihydroxy-2-butanone