PhMgBr + (CH)3C - OH →
(1) t-butyl phenyl ether
(2) Benzene
(3) Phenol
(4) t-butyl benzene
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Answer:
t- butyl benzene this is right answer
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Answer:
Benzene
Explanation:
The reaction mechanism is attached in the picture below
Generally people tend to think that the answer for this is t-butyl benzene, due to stability of 3° carbonation, but that's not the case.
The reason being, OH cannot separate itself out, it either needs a proton to hydrolysed and leave or a strong nucleophile, which grignard reagent isn't
Hope this answer helped you
P.S this is my 100th answer in chem✌
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