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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–nitrogen_bond

    Similar to carbon–carbon bonds, these bonds can form stable double bonds, as in imines; and triple bonds, such as nitriles. Bond lengths range from 147.9 pm for simple amines to 147.5 pm for C-N= compounds such as nitromethane to 135.2 pm for partial double bonds in pyridine to 115.8 pm for triple bonds as in nitriles. [2]

  3. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    As such, the predicted shape and bond angle of sp 3 hybridization is tetrahedral and 109.5°. This is in open agreement with the true bond angle of 104.45°. The difference between the predicted bond angle and the measured bond angle is traditionally explained by the electron repulsion of the two lone pairs occupying two sp 3 hybridized orbitals.

  4. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    With 133 pm, the ethylene C=C bond length is shorter than the CC length in ethane with 154 pm. The double bond is also stronger, 636 kJ mol −1 versus 368 kJ mol −1 but not twice as much as the pi-bond is weaker than the sigma bond due to less effective pi-overlap.

  5. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Molecular geometries can be specified in terms of 'bond lengths', 'bond angles' and 'torsional angles'. The bond length is defined to be the average distance between the nuclei of two atoms bonded together in any given molecule. A bond angle is the angle formed between three atoms across at least two bonds.

  6. Bond length - Wikipedia

    en.wikipedia.org/wiki/Bond_length

    Shorter than average CC bond distances are also possible: alkenes and alkynes have bond lengths of respectively 133 and 120 pm due to increased s-character of the sigma bond. In benzene all bonds have the same length: 139 pm. Carbon–carbon single bonds increased s-character is also notable in the central bond of diacetylene (137 pm) and ...

  7. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    A bond of higher bond order also exerts greater repulsion since the pi bond electrons contribute. [10] For example in isobutylene, (H 3 C) 2 C=CH 2, the H 3 CC=C angle (124°) is larger than the H 3 CC−CH 3 angle (111.5°). However, in the carbonate ion, CO 2− 3, all three C−O bonds are equivalent with angles of 120° due to resonance.

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  9. Atomic spacing - Wikipedia

    en.wikipedia.org/wiki/Atomic_spacing

    In solid materials, the atomic spacing is described by the bond lengths of its atoms. In ordered solids, the atomic spacing between two bonded atoms is generally around a few ångströms (Å), which is on the order of 10 −10 meters (see Lattice constant ).