Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?

1.	Allyl chloride is hydrolysed more readily than n-propyl chloride. Why?
Answer» <html><body><p></p>Solution :<a href="https://interviewquestions.tuteehub.com/tag/allyl-2411923" style="font-weight:bold;" target="_blank" title="Click to know more about ALLYL">ALLYL</a> chloride shows high <a href="https://interviewquestions.tuteehub.com/tag/reactivity-1178275" style="font-weight:bold;" target="_blank" title="Click to know more about REACTIVITY">REACTIVITY</a> because the <a href="https://interviewquestions.tuteehub.com/tag/carbocation-909158" style="font-weight:bold;" target="_blank" title="Click to know more about CARBOCATION">CARBOCATION</a> formed by hydrolysis is <a href="https://interviewquestions.tuteehub.com/tag/stabilised-632895" style="font-weight:bold;" target="_blank" title="Click to know more about STABILISED">STABILISED</a> by resonance while no such stabilisation of carbocation <a href="https://interviewquestions.tuteehub.com/tag/exists-979838" style="font-weight:bold;" target="_blank" title="Click to know more about EXISTS">EXISTS</a> in the case of n-propyl chloride. <br/> <img src="https://d10lpgp6xz60nq.cloudfront.net/physics_images/MOD_SPJ_CHE_XII_P2_C10_E03_082_S01.png" width="80%"/></body></html>

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