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Which one of the foloowing compound will undergo hydrolysis at a faster rate by S_(N)1mechanism ? Justify . |
Answer» Solution : will UNDERGO `S_(N)1` REACTION faster . Greater the stability of the carbocation , greater will be its ease of formation from the corresponding halide and faster will be the rate of reaction . The benzylic carbocation formed gets stablished through resonance. 1 ![]() `CH_(3)CH_(2)CH_(2)Cl` forms a `1^(@)`carbocation , which is less stable than benzylic carbocation . |
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