The total number of contributing structures showing hyperconjugation (involving $C-H$ bonds) for the following carbocation is

  • A
    $4$
  • B
    $5$
  • C
    $6$
  • D
    $7$

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Similar Questions

State True or False for the following statements:
$(i)$ The stability of carbocation is explained by the delocalized structure of hyperconjugation.
$(ii)$ The stability of carbocation is explained by drawing the resonance structure.
$(iii)$ Hyperconjugation effect is $(+)$ or $(-)$.
$(iv)$ Mesomeric effect is $(+)$ or $(-)$.

Identify the $-I$ effect causing group from the following.

The decreasing order of acidic strengths of the following compounds is:

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Orbital interaction between the $\sigma$ bonds of a substituent group and a neighbouring $\pi$ orbital is known as

In which of the following are the curved arrows not correctly mentioned to show the movement of electrons in drawing resonating structures?

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