The hyperconjugative stabilities of tert...

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

A

`sigmararr ` p ( empty ) and `sigma rarr pi^(***)` electron delocalisations

B

`sigma rarr sigma^(***)` and `sigma rarr pi ` electron delocalisations

C

`sigma rarr `p ( filled ) and `sigma rarr pi ` electron delocalisation

D

p ( filled ) `rarr sigma^(***)` electrons delocalisation

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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.