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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.why is the last part correct?
i feel like benzophenone is too sterically hindered to react again with PhMgBr and form 3 phenyl rings on one carbon via nucleophilic attack
The rings are not in the plane of the carbonyl bond I think.
oh, ok
yeah 3d models online show that both benzene rings are in the same plane, so nucleophilic attack could just happen from out of that plane
thanku
+solved @Opt
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