Oxidation of Cyclic Ketone Homework Help

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Organic chemistry is a sub stream of chemistry. It basically deals with the study of the reactions, properties, and structures of various organic and compounds in other words it is the study of different forms of matter containing carbon atoms. It teaches you about both physical and chemical properties and applies methods to analyze chemical reactivity in order to understand the behavior of the organic matter. So this is really important to know as majority of the compounds around us is organic.

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Baeyer–Villiger oxidation of cyclic ketones:

The Baeyer-Villiger oxidation which is also called Baeyer-Villiger rearrangement basically creates an ester from a lactone or creates a ketone from cyclic ketone. It is an organic reaction where the peroxides or Peroxyacids play as an oxidant. In the year 1899 the reaction was named after Victor Villiger and Adolf Baeyer who established the reaction first. You can opt Oxidation of cyclic ketone assignment help service to easily solve complicated problems on these reactions.

Oxidation of Cyclic Ketone 1” = CAqueous hydrogen peroxide acted as an oxidant on transition metal oxides by the Baeyer–Villiger oxidation of cyclic ketones was a matter of thorough investigation. Then the result showed that MoO3 and WO3 can display better catalytic activity than Fe2O3, ZnO, TiO2, Co3O4, and ZrO2. This extensive catalytic activity is due to the interaction of WO3/H2O2 and MoO3/H2O2. Moreover MoO3 and WO3’s reaction was also discovered.

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An acid/base reaction.


The nucleophilic O attacks the carbonyl C by electron shift.


The C-C bond is migrated to a new C-O bond.


Lastly you get an acid/base reaction revealing the C=O bond and it’s an ester product. Check by Image

Oxidation of Cyclic Ketone 2” = C

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