Four carbocations are shown, which can possibly rearrange via hydride shift to a more stable carbocation. Compound A consists of two fused cyclohexane rings where a carbocation is on one of the fused carbons. Compound B consists of a linear pentane chain with a carbocation on carbon 2. Compound C consists of a linear pentane chain where carbon 3 is bonded to a CH 2 plus. Compound D consists of a cyclohexene where the carbocation is on carbon 1 and an alkene on carbons 3 and 4. Select the carbocation(s) that will rearrange via hydride shift. OC OD

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Four carbocations are shown, which can possibly rearrange via hydride shift to a more stable carbocation.
Compound A consists of two fused cyclohexane rings where a carbocation is on one of the fused carbons. Compound B
consists of a linear pentane chain with a carbocation on carbon 2. Compound C consists of a linear pentane chain where
carbon 3 is bonded to a CH 2 plus. Compound D consists of a cyclohexene where the carbocation is on carbon 1 and an
alkene on carbons 3 and 4.
Select the carbocation(s) that will rearrange via hydride shift.
OC
O A
Transcribed Image Text:Four carbocations are shown, which can possibly rearrange via hydride shift to a more stable carbocation. Compound A consists of two fused cyclohexane rings where a carbocation is on one of the fused carbons. Compound B consists of a linear pentane chain with a carbocation on carbon 2. Compound C consists of a linear pentane chain where carbon 3 is bonded to a CH 2 plus. Compound D consists of a cyclohexene where the carbocation is on carbon 1 and an alkene on carbons 3 and 4. Select the carbocation(s) that will rearrange via hydride shift. OC O A
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