$A$ tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following?

  • A
    Hyperconjugation
  • B
    $ -I $ effect of $ -CH_3 $ groups
  • C
    $ +R $ effect of $ -CH_3 $ groups
  • D
    $ -R $ effect of $ -CH_3 $ groups

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Correct order of stability is

Consider the following compounds:
$(I)$ $(CH_3)_3C-CH^{\bullet}-C_6H_5$
$(II)$ $(C_6H_5)_3C^{\bullet}$
$(III)$ $2$-methylbicyclo$[2.2.1]$hept$-2-$yl radical (as shown in the image)
Hyperconjugation occurs in:

Which of the following intermediates is more stable?

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Which of the following is the least stable carbocation?

The stability of the following carbocations decreases in the order:

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