Buy custom Reac 714 Studying Sn1 And Sn2 Reactions: Nucleophilic Substitution At Saturated Carbon
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This is because it is a weaker base than the chlorine ion. Since the best leaving groups are weak bases, bromine is a weaker base than chlorine and it functions as a better leaving group.
5) The 2-bromo-2-methylpropane reacted faster in the SN1 reaction than the 2-bromopropane. This is due to the fact that after the first, slow, rate-determining step of the reaction occurs, and the bromine ion leaves, the resulting carbocations differ in stability...
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This is due to the fact that after the first, slow, rate-determining step of the reaction occurs, and the bromine ion leaves, the resulting carbocations differ in stability. A 3? carbocation is formed with the 2-bromo-2-methylpropane. On the other hand, a secondary carbocation is formed with the 2-bromopropane...
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