Using electrophilic aromatic substitution theory, explain why 4,4′-di-tert-butylbiphenyl (para position) is made when biphenyl is subjected to
Using electrophilic aromatic substitution theory, explain why 4,4′-di-tert-butylbiphenyl (para position) is made when biphenyl is subjected to Friedel-Craft alkylation conditions using tert-butyl chloride, FeCl3 and dichloromethane??
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