Explain leaving group affects the rate of an sn1 reaction

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Which alkyl halide reacted fastest: 2-chloro-2-methylpropane or 2-bromo-methylpropane? Explain how and why the nature of the leaving group affects the rate of an Sn1 reaction. Would 2-iodo-2-methylpropane react faster or slower than the other alkyl halides?

Reference no: EM13343501

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