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  2. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    The hydrogen fluoride, HF, molecule is polar by virtue of polar covalent bonds – in the covalent bond electrons are displaced toward the more electronegative fluorine atom. The ammonia molecule, NH 3, is polar as a result of its molecular geometry. The red represents partially negatively charged regions.

  3. Electronegativities of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electronegativities_of_the...

    The Nature of the Chemical Bond. 3rd ed., Cornell University Press, p. 93. 93. ^ The electronegativity of francium was chosen by Pauling as 0.7, close to that of caesium (also assessed 0.7 at that point).

  4. Electronegativity - Wikipedia

    en.wikipedia.org/wiki/Electronegativity

    Electronegativity, symbolized as χ, is the tendency for an atom of a given chemical element to attract shared electrons (or electron density) when forming a chemical bond. [1] An atom's electronegativity is affected by both its atomic number and the distance at which its valence electrons reside from the charged nucleus. The higher the ...

  5. Linear molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Linear_molecular_geometry

    Linear organic molecules, such as acetylene (HC≡CH), are often described by invoking sp orbital hybridization for their carbon centers. Two sp orbitals According to the VSEPR model (Valence Shell Electron Pair Repulsion model), linear geometry occurs at central atoms with two bonded atoms and zero or three lone pairs ( AX 2 or AX 2 E 3 ) in ...

  6. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Molecular geometry influences several properties of a substance including its reactivity, polarity, phase of matter, color, magnetism and biological activity. [1] [2] [3] The angles between bonds that an atom forms depend only weakly on the rest of molecule, i.e. they can be understood as approximately local and hence transferable properties.

  7. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonhydrogen_bond

    The length of the carbonhydrogen bond varies slightly with the hybridisation of the carbon atom. A bond between a hydrogen atom and an sp 2 hybridised carbon atom is about 0.6% shorter than between hydrogen and sp 3 hybridised carbon. A bond between hydrogen and sp hybridised carbon is shorter still, about 3% shorter than sp 3 C-H.

  8. Electron affinity (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_affinity_(data_page)

    First, as the energy that is released by adding an electron to an isolated gaseous atom. The second (reverse) definition is that electron affinity is the energy required to remove an electron from a singly charged gaseous negative ion. The latter can be regarded as the ionization energy of the –1 ion or the zeroth ionization energy. [1]

  9. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    The −1 occurs because each carbon is bonded to one hydrogen atom (a less electronegative element), and the − ⁠ 1 / 5 ⁠ because the total ionic charge of −1 is divided among five equivalent carbons. Again this can be described as a resonance hybrid of five equivalent structures, each having four carbons with oxidation state −1 and ...