What is the product of 1, 4-addition in the r | vedclass

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(A) The reaction of $HCl$ with a conjugated diene proceeds via the formation of a resonance-stabilized allylic carbocation. $1$. Protonation of the do

Vedclass · Accepted Answer

$2-$chloro$-2,5-$dimethylhex$-3-$ene

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(A) The reaction of $HCl$ with a conjugated diene proceeds via the formation of a resonance-stabilized allylic carbocation. $1$. Protonation of the double bond occurs to form the most stable carbocation. $2$. The resulting allylic carbocation has two resonance structures. $3$. $1, 4$-addition occurs when the chloride ion $(Cl^-)$ attacks the terminal carbon of the allylic system. $4$. Based on the provided reaction mechanism,the $1, 4$-addition product is $2$-chloro-$2, 5$-dimethylhex-$3$-ene.

What is the product of $1, 4$-addition in the reaction shown below?

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