bond angle

chemistry

Learn about this topic in these articles:

carbenes

  • Nonbonding orbitals in triplet and singlet states
    In carbene: Electronic configuration and molecular structure.

    The bond angle for the singlet state, however, is predicted to be larger than that for the triplet state. These predictions are fully supported by experiments. The simplest carbene, methylene, has been shown by a technique called electron magnetic resonance spectroscopy to have a triplet ground…

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hydrocarbons

  • structures of common hydrocarbon compounds
    In hydrocarbon: Cycloalkanes

    …smaller than the normal tetrahedral bond angle of 109.5° and imposes considerable strain (called angle strain) on cyclopropane. Cyclopropane is further destabilized by the torsional strain that results from having three eclipsed C―H bonds above the plane of the ring and three below.

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molecular shape

  • crystal bonding
    In chemical bonding: Applying VSEPR theory to simple molecules

    The angle between electron pairs in a tetrahedral arrangement is 109.5°. However, although H2O is indeed angular and NH3 is trigonal pyramidal, the angles between the bonds are 104° and 107°, respectively. In a sense, such close agreement is quite satisfactory for so simple an approach,…

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potential energy curve

  • crystal bonding
    In chemical bonding: The quantum mechanics of bonding

    …varies as bond lengths and bond angles are changed. A typical curve for a diatomic molecule, in which only the internuclear distance is variable, is shown in Figure 10. The energy minimum of this curve corresponds to the observed bond length of the molecule. The depth of the minimum is…

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structure and classification of alcohols

  • cholesterol
    In alcohol: Structure and classification of alcohols

    … atoms, however, so the R―O―H bond angle in alcohols is generally larger than the 104.5° H―O―H bond angle in water. For example, the 108.9° bond angle in methanol shows the effect of the methyl group, which is larger than the hydrogen atom of water.

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