front 1 Formation of Cyanohydrin From ketones/Aldehydes Product: OH/CN | back 1 ![]() |
front 2 Hydrate/ Gem-doil formation from aldehydes/ketones Product: 2 OH Reagent: H2O | back 2 ![]() |
front 3 Reaction between aldehydes/ketones and HX Product: HX and OH (x = F, Br, I, Cl) Regeant: HX | back 3 ![]() |
front 4 Grignard Regeant Reaction between Aldehydes/ketones Product: OH Reagent: RMgX/H3O | back 4 ![]() |
front 5 Organolithium Reagent Reaction between Aldehydes/ketones Product: OH Reagent: | back 5 ![]() |
front 6 Reduction of Aldehydes Product: OH Reagent: LiAlH4/H3O+ | back 6 ![]() |
front 7 Reduction of Aldehydes Product: OH Reagent: NaBH4/ EtOH | back 7 ![]() |
front 8 Reduction of Ketones Product: OH Reagent: NaBH4/ EtOH & | back 8 ![]() |
front 9 Reduction of Ketones Product: OH Reagent: LiAlH4/H3O+ | back 9 ![]() |
front 10 Aldehyde/Ketone Reduction using NADH & enzyme catalysts Product: OH Reagent: NADH/enzyme | back 10 ![]() |
front 11 Clemmensen reduction Product: More H Reagent: Zn(Hg)/ HCL | back 11 ![]() |
front 12 Oxidation of aldehydes to COOH(carboxylic acids) Product: COOH Reagent: (KMnO4, OH-/ H3O+) + more--> | back 12 ![]() |
front 13 Baeyer Villiger reaction: Ketone to esters Product: esters Reagent: CF3Co3H | back 13 ![]() |
front 14 Baeyer Villiger reaction: Aldehydes to Carboxylic acids Product: COOH Reagent: CF3CO3H | back 14 ![]() |