Solution
Core Logic
Let's analyze the statements: Statement A: Resonating structure with more covalent bonds and lesser charge separation are indeed more stable. (True)
Statement B: In the electromeric effect, when the pi electrons shift towards the attacking reagent (electrophile), it's +E. When they shift away from the attacking reagent (nucleophile), it's -E. The statement says +E with nucleophile and -E with electrophile, which is reversed. (False)
Statement C: Inductive effect is a permanent polarization that contributes to the dipole moment and intermolecular forces, thereby influencing boiling/melting points. (True)
Statement D: The greater the number of alkyl groups attached to the double bond, the more stable the alkene is (due to hyperconjugation). More stable alkenes release LESS energy upon hydrogenation, meaning they have a LOWER heat of hydrogenation. (False)
Statement E: Stability of a carbanion increases with the s-character of the carbon atom because an orbital with more s-character is closer to the nucleus, stabilizing the negative charge better (sp > sp² > sp³). (True)
Step 1: Conclusion
Statements B and D are NOT true.
Pattern Recognition
Heat of Hydrogenation (HOH) is inversely proportional to alkene stability. More substituted alkene = more stable = lower HOH.
Chapter Mix
Class 11 Chemistry: Organic Chemistry Some Basic Principles and Techniques