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(ch)3ch-ch2br in presence of ethanol should undergo sn1 because 1 degree Halide is connected to β 3 degree carbon but answer is sn2 why?
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(ch)3ch-ch2br in presence of ethanol should undergo sn1 because 1 degr...
It must be show SN2 mechanism... However the C atom containing halogen atom is surrounded by three methyl groups that provides the large steric hinderence to the incoming hydroxyl group so the approach of hydroxyl group is very difficult by these way. Also, the tert butyl carbonium ion formed in step one of SN1 mechanism is very stable due to +I effect of three -CH3 groups.so it follows SN1 instead of SN2 mechanism.
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(ch)3ch-ch2br in presence of ethanol should undergo sn1 because 1 degree Halide is connected to β 3 degree carbon but answer is sn2 why?
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