I need to find the products for 2,2-Dimethyl-1-propanol. I know that a rearrangement occurs to give the more stable carbocation. However, from then on, how do I know which hydrogen I should pluck off to get the products? I can see 3 sources, the two methyl group and the CH2. Any help please? Also, it's not just for this question, I've been doing others and face this delimma also. Is there a rule to determine which C I should form the double bond with, if there are multiple carbons which I can take the hydrogen off of?
2007-11-14
09:21:53
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2 answers
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asked by
Reimei
2