The correct order of stability of the carbocations given below is:

  • A
    $(i) > (ii) > (iii) > (iv)$
  • B
    $(ii) > (iii) > (i) > (iv)$
  • C
    $(ii) > (i) > (iii) > (iv)$
  • D
    $(i) > (iii) > (ii) > (iv)$

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Similar Questions

The order of decreasing ease of abstraction of hydrogen atoms in the following molecule is:

For the given reaction,the total number of possible products formed by the tertiary carbocation of $A$ is $.........$.

Consider the following compound $(X)$:
$H-C \equiv C-CH_2-CH(CH_3)-CH_3$
The most stable and least stable carbon radicals,respectively,produced by homolytic cleavage of the corresponding $C-H$ bond are:

Which of the following represents the incorrect stability order?

Consider the following statements. Of these statements:
$(I) \ CH_3O-CH_2^+$ is more stable than $CH_3-CH_2^+$
$(II) \ Me_2CH^+$ is more stable than $CH_3-CH_2-CH_2^+$
$(III) \ CH_2=CH-CH_2^+$ is more stable than $CH_3-CH_2-CH_2^+$
$(IV) \ CH_2=CH^+$ is more stable than $CH_3-CH_2^+$

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