The structure of the compound that gives a tr | vedclass

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(C) When phenols are treated with bromine water,the $-OH$ group strongly activates the benzene ring,leading to electrophilic substitution at all avail

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(C) When phenols are treated with bromine water,the $-OH$ group strongly activates the benzene ring,leading to electrophilic substitution at all available ortho and para positions. For $m$-cresol ($3$-methylphenol),the positions ortho and para to the $-OH$ group are available for substitution. Specifically,the positions ortho to the $-OH$ group (at $C2$ and $C6$) and the position para to the $-OH$ group (at $C4$) are all activated,leading to the formation of $2,4,6-$tribromo$-3-$methylphenol. Therefore,$m$-cresol gives a tribromo derivative.

The structure of the compound that gives a tribromo derivative on treatment with bromine water is

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