Current Attempt in Progress The compound below can react rapidly via an Sw1 process: OTS Select the explanation of why this primary substrate will undergo an Sy1 reaction so rapidly. O The rate of the reaction is a result of the strong leaving group. O The E of the first step of the mechanism is lower than the E, of the second step. O The methyl substrate has little steric hindrance and a lower-energy transition state. O When the leaving group leaves, the carbocation formed is resonance stabilized.

Current Attempt in Progress The compound below can react rapidly via an Sw1 process: OTS Select the explanation of why this primary substrate will undergo an Sy1 reaction so rapidly. O The rate of the reaction is a result of the strong leaving group. O The E of the first step of the mechanism is lower than the E, of the second step. O The methyl substrate has little steric hindrance and a lower-energy transition state. O When the leaving group leaves, the carbocation formed is resonance stabilized.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter24: Amines And Heterocycles

Section24.SE: Something Extra

Problem 42MP

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