SOLVED: In reactions of carbonyl compounds under basic conditions, the base removes a proton from the α carbon of the carbonyl compound, forming an enolate ion. The enolate ion has two resonance contributors. In the box on the right, draw the best resonance structure of the enolate ion on the left. Draw electron-flow arrows on the structure on the left to indicate how the electrons reorganize to give the structure on the right.H₃C-CH₃Draw all missing reactants and/or products in the appropr

Carbonyl Functional Group | Properties, Compounds & Structure

Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like aldehydes or ketones. Why? - Chemistry | Shaalaa.com

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