The compound is an aromatic ketone having a phenyl group directly attached to the carbonyl group; its chemical formula is C9H10O and its structural formula is COCH3C6H4CH3.
Reduction occurs either by metal hydrides such as LAH or by hydrogen; ketones are reduced to secondary alcohols. The statement in the article is arguable because reduction and not oxidation occurs with either compound yielding a secondary alcohol. Catalytic hydrogenation or reduction by hydrogen is synonymous names for the same reaction; which is valid. Tollen's reagent is a reagent used to distinguish between aldehydes and ketones. Ketones do not react with the reagent which the author failed to demonstrate. P-methyacetophenone reacts to form a tertiary alcohol with ethylmagnesium bromide; this point is accurate. The compound reacts with Grignard reagent giving magnesium alkoxide which then yields the tertiary alcohol when water is added to it. All in all, p-metyacetophenone is a compound used in perfumes and its synthesis is of great importance for the chemists.
Calibrated Peer Review (CPR) Site. 31 Nov. 2000. The National Scrutinizer. Volume 88, Number 9. A New Compound Has Been Synthesized! 04 Mar. 2009.