(CH3)3COH + H+ --> (CH3)3C+
This electrophile will attack the phenol.
As phenol has o-p directing grp,
ortho as well as para product will form with para as major product because of steric hindrance
(CH3)3COH + H+ --> (CH3)3C+
This electrophile will attack the phenol.
As phenol has o-p directing grp,
ortho as well as para product will form with para as major product because of steric hindrance
There will be an -O also in the new added group at the joining position
A type of FC alkylation....OH will be protonated and leave, and the tert butyl carbocation will attack phenol at para position. Asish is correct.