Disclaimer The questions posted on the site are solely user generated, Doubtnut has no ownership or control over the nature and content of those questions. Doubtnut is not responsible for any discrepancies concerning the duplicity of content over those questions. Solution : Compound (B) will give `S_(N)1` reaction faster than compound (A) because `S_(N)1` reaction depends upon the stability of carbocation. Benzyl chloride on lonisation gives `C_(6)H_(5)overset(+)CH_(2)` carbocation which is resonance srabilised while the carbocation obtained from compound (A) is not stabilised by resonance. <br> <img src="https://d10lpgp6xz60nq.cloudfront.net/physics_images/ARH_NCERT_EXE_CHM_XII_C10_S01_064_S01.png" width="80%"> Related Chemistry Q&AFind answers to questions asked by students like you. Q: Which pathway will this reaction likely take? NaSH ? SN1 O SN2 O E1 E2 A: Click to see the answer Q: Will each of the following reactions follow an El or E2 mechanism? 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Which one of the following compounds will undergo the fastest sn1 reaction?
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