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JEE Advanced 2013Paper 1
Exam
JEE Advanced
Year
2013
Paper
Paper 1
Subject
Chemistry
Chapter
General Organic Chemistry

JEE Advanced 2013 · Paper 1 · Chemistry · General Organic Chemistry

The hyperconjugative stabilities of tert-butyl cation and 2-butene,...

The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due toThe hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due toThe hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to

Options

  1. Aσ \to \text{p} (empty) and σ \to {π}^{*} electron delocalisations.
  2. Bσ \to {σ}^{*} and σ \to π electron delocalisations.
  3. Cσ \to \text{p} (filled) and σ \to π electron delocalisations.
  4. D\text{p (filled)} \to {σ}^{*} and σ \to {π}^{*} electron delocalisations.

Correct answer

A. σ \to \text{p} (empty) and σ \to {π}^{*} electron delocalisations.

Step-by-step solution

The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to 
In tert-butyl cation, carbon bearing ⊕⊕ charge has one vacant p orbital hence it is \sigma−p\text{\sigma} - \text{p} (empty) conjugation or Hyperconjugation.
The hyperconjugative stabilities of tert-butyl cation and 2-butene, respectively, due to 
In 2-butene hyperconjugation between \sigma\text{\sigma} and π∗{π}^{*} bond.
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