Another side note! H2O2 can be used in the work up to give the corresponding carboxylic acids, and if a reducing agent like NaBH4 (Zn isn't strong enough) is used then you will get the corresponding alcohol.
Like Dan said, dimethylsulfide ((CH3)2S) is used to get the corresponding carbonyl (aldehyde/ketone) compounds. I would say dimethylsulfide is a more common reagent for this purpose, than Zn.