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Organic Chemistry structural elucidation question.

When aqueous bromine is added to an organic dyestuff P, C10H14O, bromine is decolourised
and compound Q, C10H14OBr4, is formed. P is insoluble in aqueous NaOH. Both P and Q
give silver precipitates when reacted with Tollen’s reagent. When P is treated with hot
acidified potassium manganate(VII), two organic products, R, C3H4O3, and S, C7H10O5, are
formed. R gives a pale yellow precipitate when warmed with alkaline aqueous iodine.
Treatment of S with LiAlH4 produces a compound with the structure below.

CH2OH

HOCH2
O

Suggest the structures of P, Q, R and S, giving your reasoning.
[6]

P is
CHO

CHO

CH3

or

CH3