Acylation, H+ from Hcl attack on ketone
Forming 3 degree carbo+,then EAS
but how h+ will attack on electrophilic caron or carbonyl carbon.
i didnt get it bro will you elaborate it
Edit:- didnt saw the answer
which typical condensation are they talking about.
Though i undersrood the mechanism to get this product but couldnt think of reason why 2 equivalents of phenol is used,this reaction is similar to fridel carft
yeah i am also not getting it why it is so.