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28) The reaction of tert-butyl bromide, (CH,)CBr, with ethanol affords the substitution product tert-butyl ethyl ether, (CH)1
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Ans 28 : A) The rate remains the same

The reactant tert-butyl bromide is a tertairy halide so it will undergo a SN1 mechanism. SN1 mechanism occurs in two steps and the rate of reaction depends only on the reactant and not on nucleophile.

So increasing the concentration of ethanol , will not affect the rate of reaction.

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