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Aromatic bromination catalyzed by the Lewis acid thallium acetate (Tl(OOCCH3)3 gives only the para isomer. Suggest an explanation for this regioselectivity Aromatic bromination catalyzed by the Lewis acid thallium acetate (Tl(OOCCH3)3 gives only the para isomer. Suggest an explanation for this regioselectivity
Since you have not mentioned the functional group already attached to the benzene ring, A possible explanation is that the functional group attached must be a ortho para director and might be bulky therefore, not supporting the ortho isomer.Thanks and RegardsApoorva AroraIIT RoorkeeaskIITians Faculty
Since you have not mentioned the functional group already attached to the benzene ring, A possible explanation is that the functional group attached must be a ortho para director and might be bulky therefore, not supporting the ortho isomer.
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