Chemistry, 07.12.2019 02:31 hadwell34

Carbons 1 and 4 of 1,3−cyclopentadiene are equivalent and give the same carbocation on protonation. likewise, carbons 2 and 3 are equivalent. write the structure of the carbocation formed by protonation of c−2 or c−3 to verify that it is not allylic and therefore not as stable as the one formed by protonation of c−1 or c−4.

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Carbons 1 and 4 of 1,3−cyclopentadiene are equivalent and give the same carbocation on protonation....

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