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  • https://chem.libretexts.org/Courses/Prince_Georges_Community_College/CHEM_2000%3A_Chemistry_for_Engineers_(Sinex)/Unit_2%3A__Molecular_Structure/Chapter_5%3A_Molecular_Geometry/Chapter_5.4%3A__Polyatomic_Systems_Multiple_Bonds_Resonance
    For π bonds between two atoms (as in ethylene or acetylene), the resulting molecular orbitals are virtually identical to the π molecular orbitals in diatomic molecules such as O 2 and N 2 . Applying t...For π bonds between two atoms (as in ethylene or acetylene), the resulting molecular orbitals are virtually identical to the π molecular orbitals in diatomic molecules such as O 2 and N 2 . Applying the same approach to π bonding between three or four atoms requires combining three or four unhybridized np orbitals on adjacent atoms to generate π bonding, antibonding, and nonbonding molecular orbitals extending over all of the atoms.
  • https://chem.libretexts.org/Bookshelves/General_Chemistry/General_Chemistry_Supplement_(Eames)/Valence_Bond_Theory/Multiple_Bonds
    If you remember the idea of resonance energy you might expect that the availability of 3 different structures with the same energy allows resonance between the structures, so that each bond is actuall...If you remember the idea of resonance energy you might expect that the availability of 3 different structures with the same energy allows resonance between the structures, so that each bond is actually 4/3 of a bond, and the molecule is much more stable because of the resonance energy.

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