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The delocalization of $\sigma$ electrons of $C-H$ bond of an alkyl group with the $\pi$ electrons of benzene is observed in

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Given below are two statements $:$
Statement $I :$ Hyperconjugation is not a permanent effect.
Statement $II :$ In general,greater the number of alkyl groups attached to a positively charged $C$ atom,greater is the hyperconjugation interaction and stabilization of the cation.
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In which $C-C$ bond of $CH_3-CH_2-CH_2-Br$,the inductive effect is expected to be the least?

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