The enol carbon or ∝-carbon nucleophile attacks at molecular bromine in the acid-catalyzed α-bromination of a ketone
Treatment of ketones with bromine in the presence of acid will results in formation of a new C-Br bond at the alpha position. The purpose of the acid is to catalysed formation of the enol from ketone , which is active nucleophile in the reaction. This reaction is called haloform reaction which is used to identify the methyl substituted ketone in the presence of aldehyde.
learn more about ketone
brainly.com/question/4439718
#SPJ4
Kinetic. Transform to chemical energy in muscles