Which of the following can show hyperconjugation?

  • A
    $CH_3-C(CH_3)_2-C^\bullet H_2$
  • B
    $CH_3-C^\bullet(CH_3)-CH_3$
  • C
    $CH_2=CH-C^\bullet H_2$
  • D
    Benzyl radical $(C_6H_5-C^\bullet H_2)$

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Similar Questions

Arrange the following carbanions in decreasing order of stability $:$

Which acid of each pair shown here would you expect to be stronger?
$(i)$ $CH_3CO_2H$ or $CH_2FCO_2H$
$(ii)$ $CH_2FCO_2H$ or $CH_2ClCO_2H$
$(iii)$ $CH_2FCH_2CH_2CO_2H$ or $CH_3CHFCH_2CO_2H$
$(iv)$ $F_3C-C_6H_4-COOH$ or $H_3C-C_6H_4-COOH$

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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 $(-)$.

Which one of the nitrogen atoms in $H_2N-NH-CO-NH_2$ (where the atoms are labeled $I, II, III$ as shown in the structure) is the most nucleophilic?

Identify the lowest positive charge developed (indicated by $\delta, \delta_1, \delta_2, \delta_3$) due to the inductive effect in the following compound: $CH_3-CH_2-CH_2-CH_2-Cl$.

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