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Explain carbocation intermediate
When 3-methyl-1-butene undergoes acid-catalyzed hydration, rearrangement happens because carbocation intermediates are included. (See the solution) Oxymercuration-reduction gives addition without rearrangement because the intermediate is a cyclic mercurinium ion, which does not rearrange.
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Explain CMR spectrum 2,2-Dimethyl-1-propanamine (neopentylamine, (CH 3 ) 3 CCH 2 NH 2 ) has a maximum of three resonances in its CMR spectrum. 2-Methyl-2-butanamine, CH 3 CH 2
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