Why is 1,3-octadiene more reactive towardelectrophilic hydration, than 1,7-octad

Question

Why is 1,3-octadiene more reactive towardelectrophilic hydration, than 1,7-octadiene? A. Hydration of conjugated dienesproceeds through a more stable carbocation B. Conjugated dienes are morestable, than non-congujated dienes C. The final product of hydrationof conjugation dienes is more stable
D. Or all the above? Why is 1,3-octadiene more reactive towardelectrophilic hydration, than 1,7-octadiene? Why is 1,3-octadiene more reactive towardelectrophilic hydration, than 1,7-octadiene? A. Hydration of conjugated dienesproceeds through a more stable carbocation B. Conjugated dienes are morestable, than non-congujated dienes C. The final product of hydrationof conjugation dienes is more stable
D. Or all the above? A. Hydration of conjugated dienesproceeds through a more stable carbocation B. Conjugated dienes are morestable, than non-congujated dienes B. Conjugated dienes are morestable, than non-congujated dienes C. The final product of hydrationof conjugation dienes is more stable
D. Or all the above? C. The final product of hydrationof conjugation dienes is more stable
D. Or all the above?

Explanation / Answer

A. Hydration of conjugated dienes proceeds through a more stablecarbocation

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