The correct option is A I>II>III>IV>V
Structure (I) is aromatic.
Structure (II) shows-l effect due to presence of N(CH3)3 group, which destabilizes the carbocation.
Structure (III) shows-l and R-effects, which destabilizes the carbocation more.
Structure(IV) contains positive charge on its ring. Hence, it is less stable than structures I, II and III.
Structure (IV) contains positive charge with triple bond, which has high tendency to gain electrons. Hence, it is least stable among all.
∴ Decreasing order of stability I>II>III>IV>V.