Which of the following is correct stability order of alkenes?
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In alkene stability questions, always rank based on:
(1) degree of substitution,
(2) trans $>$ cis (due to less steric hindrance), and
(3) hyperconjugation effects.
The stability of alkenes is influenced primarily by:
Hyperconjugation Alkyl substitution (more substituted alkenes are more stable)
Steric hindrance (cis isomers are usually less stable than trans)
Let’s analyze each alkene:
1. Isobutene (2-methylpropene):
A highly substituted (trisubstituted) alkene. It benefits from both +I effect and extensive hyperconjugation. ⇒ Highest stability2. Trans-2-butene:
Disubstituted alkene with groups on opposite sides — less steric hindrance than cis. More stable than cis-2-butene.
3. Cis-2-butene:
Also disubstituted but with steric repulsion due to same-side substituents. Less stable than trans.
4. But-1-ene:
Monosubstituted alkene, minimal hyperconjugation and substitution. ⇒ Least stable among the givenCorrect Stability Order:
\[
\text{Isobutene} > \text{Trans-2-butene} > \text{Cis-2-butene} > \text{But-1-ene}
\]