The correct stability order of the following resonance structures of CH3−CH=CH−CHO is
(A)II > III > I
(B)III > II > I✓ Correct
(C)I > II > III
(D)II > I > III
Answer: (B)
Solution
Structure III has no charge separation (all covalent bonds, non-polar), making it the most stable resonance structure. Between the two charge-separated structures, structure II places the negative charge on oxygen (more electronegative) while structure I places it on carbon (less electronegative); a negative charge is better accommodated on the more electronegative atom, so II is more stable than I.
Stability order: III > II > I.
JEE Main · 2024 · 09 Apr 2024 · Shift 2 · Single correct option