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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 delocalisatons.

B

`sigma rarrsigma^("*") and sigma rarrpi` electron delocalisations.

C

`sigma rarrp` (filled ) `sigma rarrpi` electron delocalisations.

D

p (filled ) `rarr sigma^("*") and sigma rarrpi^("*")` electron delocalisations.

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The correct Answer is:
A
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(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.

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