Acid catalysed dehydration of tertiary butyl alcohol occurs faster than n butyl alcohol why
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dehydration of alcohols undergoes through the formation of carbocation intermediate. t-butyl alcohol forms t-butyl cation which is a stable carbocation..so it undergoes dehydration at higher rate.
In case n-butanol it forms less stable carbocation n-butyl cation..which farther undergoes hydride shift to from stable carbocation..but the after accepting protone it forms n-butyl cation and which generate in a slower rate as the intermediate carbocation is not stable..
Thats the reason t-butyl alcohol under goes dehydration at faster rate
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