Consider the hydrogen cyanide molecule, HCN. If we orient this linear molecule so it is along the x axis, what orbitals on carbo
n are involved in the formation of the sp hybrid?
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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:
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: