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In substitution reactions, (CH3)3C-I reacts at the same rate with Br- and Cl- even though Br- is a more reactive nucleophile than Cl-. Why?A. (CH3)3C-Br reacts by SN1 mechanism whose rate is independent of nucleophile reactivity. B. (CH3)3C-Br reacts by SN2 mechanism and therefore all nucleophiles react at the same rate regardless of their reactivity. C. The t-butyl carbocation is so reactive, the measurable rate of it's reaction with different nucleophiles is imperceptible. D. The t-butyl group sterically hinders nucleophiles, making different nucleophiles appear to react at the same rate.
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In substitution reactions, (CH3)3C-I reacts at the same rate with Br- and Cl- even though Br- is a m...
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