Which mechanism of reactions is shown by carbonyl compounds?

Explanation

The main reactions of the carbonyl group are nucleophilic additions to the carbon‐oxygen double bond. This addition consists of adding a nucleophile and a hydrogen across the carbon‐oxygen double bond. An electrophilic addition reaction is an addition reaction where, in a chemical compound, a π bond is broken and two new σ bonds are formed. The substrate of an electrophilic addition reaction must have a double bond or triple bond. Electrophilic substitution reactions are chemical reactions in which an electrophile displaces a functional group in a compound. Free radicals are atoms or groups of atoms which have a single unpaired electron. A free radical substitution reaction is one involving these radicals. Free radicals are formed if a bond splits evenly - each atom getting one of the two electrons. The name given to this is homolytic fission.