most probably,bulky groups present on nucleophilic centre might form less stable carbocation due to steric effect .thus, isopropyl bromide would hv a faster SN1 rkn.
Its a highly silly doubt....I know weaker bases are better leaving groups what if the leaving group is the same, then which of the two orgainc compunds would give a faster rxn ?
for example :- which out of the following two would give a faster sn1 rxn
Isoprolybromide or Isobutylbromide?
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2 Answers
aieeee
·2009-06-19 11:33:58
kartik sondhi
·2009-06-20 10:18:03
yes in SN1 reactions the reaction is governed by factor of steric hindrance so isopropyl bromide would give a faster reaction