The haloform reaction predicts yellow precipitates with NaOI, specifically with methyl ketones, alcohols with adjacent methyl groups, and certain aldehydes.
A. Phenylethanone (Acetophenone): Possesses a methyl group adjacent to a carbonyl, enabling the haloform reaction and the formation of iodoform (yellow precipitate).
B. Sec-Butyl alcohol: Oxidizes to a methyl ketone with an adjacent methyl group, which undergoes the haloform reaction to produce iodoform.
C. Phenylethanal: An aldehyde with an adjacent methyl group, capable of participating in the haloform reaction and forming yellow precipitates.
D. Methyl n-propylketone: Lacks the required methyl group adjacent to the carbonyl for the haloform reaction, thus will not yield yellow precipitates.
Compounds A, B, and C will produce yellow precipitates with NaOI. The correct answer is: A, B, and C only
From the following, how many compounds contain at least one secondary alcohol? 