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.
Chapter24: Amines And Heterocycles
Section24.SE: Something Extra
Problem 42MP
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