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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Chemistry, 21.06.2019 20:30
This chart represents the melting point of several substance. what besy explains the high melting point of the salt?
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Chemistry, 22.06.2019 19:30
Estimate the molar mass of the gas that effuses at 1.6 times the effusion rate of carbon dioxide.
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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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