Class I Carbonyl compounds can be divided into two classes. Carbonyl compounds I are those in which the acyl group is attached to an atom or a group that can be replace by another group. Carboxylic acids, acyl alides, acid anhydrides, esters, -Cl, -Br, -O(CO)R, -OR, -NH2, -NHR, or -NR2 that can be replaced by a nucleophile. Acyl halides, acid anhydrides, esters, and amides are all called carboxylic acid derivatives because they differ from a carboxylic acid only in the nature of the group that has replaced the OH group of the carrboxylic acid.
Class II carbonyl compounds are those in which the acyl group is attached to a group that cannot be readily replaced by another group. Aldehydes and ketones belong to this class. The -H and alkyl or aryl (-R or -Ar) groups of aldehydes and ketones cannot be replaced by a nucleophile.
Class III carbonyl compounds Reactions at the a-Carbon. Having a tough time ... here. aldehydes, ketones, esters, and N,N-disubstituted amides have a second site of reactivity. A hydrogen bonded to a carbon adjacent to a carbonyl carbon.
Just getting all the reactions together with whom and where???