Answer:
Four substitution products are obtained. The carbocation that forms can react with either nucleophile (H2O or CH3OH) from either the top or bottom side of the molecule
Explanation:
An SN1 reaction usually involves the formation of a carbocation in the slow rate determining step. This carbocation is now attacked by a nucleophile in a subsequent fast step to give the desired product.
However, the product is obtained as a racemic mixture because the nucleophile may attack from the top or bottom of the carbocation hence both attacks are equally probable.
The attacking nucleophile in this case may be water or CH3OH
Answer:
Its C
Explanation:
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Phosgene on reacting with <span>phenylmagnesium bromide generates
benzoyl chloride.
Since, </span>phenylmagnesium bromide is added in excess. It would further react with benzoyl chloride to form
benzophenone.
Benzophenone on further reacting with phenylmagnesium bromide, and aqueous treatment, gives
triphenylmethanol.
Entire reaction pathways is shown below:
33233728793278237876548742787874578378572098-2932-=93788784787489
Answer:
I don’t know this answer sorry
Explanation: