Carbocations are important intermediates in organic reactions, they are often stabilised by resonance, inductive effect and hyperconjugation. The cation that can be stabilised by hyperconjugation is

The correct order of stability of given carbocation is:

Which of the following carbocations is most stable?

Choose the correct statement regarding the formation of carbocations A and B given :-

The decreasing order of the stability of the following carbocations is

The stability order of the above carbocations is 

Arrange the following carbocations in decreasing order of stability.

Assertion (A): Tertiary carbocations are more reactive than secondary and primary carbocations.

Reason (R): Hyper conjugation, as well as inductive effect due to additional alkyl groups stabilise tertiary carbocations.

Consider the following carbocations

(a) ${\mathrm{Cl}}_3{\mathrm{C}}^{+}$

(b) ${\mathrm{Cl}}_2{\mathrm{CH}}^{+}$

(c) ${{\mathrm{ClCH}}_2}^{+}$

(d) ${{\mathrm{CH}}_3}^{+}$

The stability sequence follows the order 

Which of the following is most stable$?$

The most stable carbocation for the following is: