A carbonyl compound X (C_8H_8O) gives a yello | vedclass

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(C) The carbonyl compound $X$ has the molecular formula $C_8H_8O$. Since it gives a yellow precipitate with $NaOI$ (iodoform test),it must contain a $

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(C) The carbonyl compound $X$ has the molecular formula $C_8H_8O$. Since it gives a yellow precipitate with $NaOI$ (iodoform test),it must contain a $CH_3CO-$ group or a $CH_3CH(OH)-$ group. Given it is a carbonyl compound,it must be acetophenone $(C_6H_5COCH_3)$. When acetophenone reacts with methanol $(CH_3OH)$ in the presence of dry $HCl$,it forms a hemiacetal. The reaction is: $C_6H_5COCH_3 + CH_3OH \xrightarrow{dry \ HCl} C_6H_5C(OH)(OCH_3)CH_3$. Comparing this with the given options,the structure in option $C$ represents the hemiacetal $1$-methoxy-$1$-phenylethanol.

$A$ carbonyl compound $X$ $(C_8H_8O)$ gives a yellow precipitate with $NaOI$. The hemiacetal of $X$ with methanol/dry $HCl$ is:

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