What is the structure of the major product wh | vedclass

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(A) Phenol has an activating (electron-releasing) $-OH$ group,which strongly activates the benzene ring towards electrophilic substitution. Bromine wa

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(A) Phenol has an activating (electron-releasing) $-OH$ group,which strongly activates the benzene ring towards electrophilic substitution. Bromine water provides $Br^{+}$ ions easily. Due to the high reactivity of phenol,the reaction does not stop at the mono- or di-bromo stage but proceeds to form a fully brominated product,$2,4,6-	ext{tribromophenol}$,as a white precipitate.

What is the structure of the major product when phenol is treated with bromine water?

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