The hyperconjugative stabilities of tert-butyl cation and $2$-butene, respectively, are due to
The hyperconjugative stabilities of tert-butyl cation and $2$-butene, respectively, are due to
- [IIT 2013]
- A
$\sigma \rightarrow p$ (empty) and $\sigma \rightarrow \pi^{\star}$ electron delocalisations.
- B
$\sigma \rightarrow \sigma^*$ and $\sigma \rightarrow \pi$ electron delocalisations.
- C
$\sigma \rightarrow p$ (filled) and $\sigma \rightarrow \pi$ electron delocalisations.
- D
$p$ (filled) $\rightarrow \sigma^{\star}$ and $\sigma \rightarrow \pi^*$ electron delocalisations.
Similar Questions
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- [AIEEE 2007]
The pairs of species of oxygen and their magnetic behaviour are noted below. Which of the following presents the correct description ?
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- [AIPMT 2011]
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