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I am trying to figure out the mechanism (i.e. E2 or E1) by which α,α-dialkylbenzyl bromides (such as A, below) undergo elimination with triethylamine. Describe two experiments (with the specific molecules to be used) that I can run to help me reach a conclusion, and what results I’d be looking for in each case

.H triethylamine RR R, R = alkyl group

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Answer #1

7 .R.1 bave to weak bene y arburation + went base = Benzs carbocation + Naost D Toer = strong base = E21 ď wholla Coll (Es) 3

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