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Consider the electrophilic addition of one equivalent of HBr to 1-methylcyclopentadiene (1). Under the reaction conditions, all possible allylic carbocations form, but there are no carbocation rearrangements. Which is the kinetically favored product? Br Br Br Br Select one: a. a O b. b C. C O d. d e. e

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t31 Allyl casbocatia one hyper (ayagaion. Two hpe (ayugettos Structure

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Consider the electrophilic addition of one equivalent of HBr to 1-methylcyclopentadiene (1). Under the reaction conditions,...
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