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The hyperconjugative stabilities of tert...

The hyperconjugative stabilities of tert-butyl cation and `2`-butene, respectively, are due to

A

`sigmararrp` (empty) and `sigmararrpi^(**)` electron delocalisations.

B

`sigmararrsigma^(**)` and `sigmararrpi` electron delocalisations.

C

`sigmararrp` (filled) and `sigmararr pi` electron delocalisations.

D

P (filled) `rarrsigma^(**)` and `sigmararrpi^(**)` electron delocalisations.

Text Solution

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The correct Answer is:
A
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|| Hyperconjugation revision || stability comparison OF alkene and carbocation ||

(A) tert-Butyl methyl ether on cleavage with HI at 373K gives tert-butyl iodide and methanol. (R ) The reaction occurs by S_(N^(2)) mechanism.