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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    A simpler method has been proposed for constructing Lewis structures, eliminating the need for electron counting: the atoms are drawn showing the valence electrons; bonds are then formed by pairing up valence electrons of the atoms involved in the bond-making process, and anions and cations are formed by adding or removing electrons to/from the ...

  3. Lone pair - Wikipedia

    en.wikipedia.org/wiki/Lone_pair

    Lone pairs (shown as pairs of dots) in the Lewis structure of hydroxide. In chemistry, a lone pair refers to a pair of valence electrons that are not shared with another atom in a covalent bond [1] and is sometimes called an unshared pair or non-bonding pair. Lone pairs are found in the outermost electron shell of atoms.

  4. Unpaired electron - Wikipedia

    en.wikipedia.org/wiki/Unpaired_electron

    In chemistry, an unpaired electron is an electron that occupies an orbital of an atom singly, rather than as part of an electron pair. Each atomic orbital of an atom (specified by the three quantum numbers n, l and m) has a capacity to contain two electrons ( electron pair ) with opposite spins .

  5. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Lewis structures (or "Lewis dot structures") are flat graphical formulas that show atom connectivity and lone pair or unpaired electrons, but not three-dimensional structure. This notation is mostly used for small molecules. Each line represents the two electrons of a single bond. Two or three parallel lines between pairs of atoms represent ...

  6. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    In the electron-donating case, the SOMO interacts with the lower energy lone pair to form a new, lower-energy, filled, delocalized bond orbital and a new, higher-energy antibonding SOMO (in net, a three-electron bond). Because the new bonding orbital contains more electrons than the SOMO, the resulting electronic state reduces molecular energy.

  7. Delocalized electron - Wikipedia

    en.wikipedia.org/wiki/Delocalized_electron

    In the simple aromatic ring of benzene, the delocalization of six π electrons over the C 6 ring is often graphically indicated by a circle. The fact that the six C-C bonds are equidistant is one indication that the electrons are delocalized; if the structure were to have isolated double bonds alternating with discrete single bonds, the bond would likewise have alternating longer and shorter ...

  8. Electron configuration - Wikipedia

    en.wikipedia.org/wiki/Electron_configuration

    In atomic physics and quantum chemistry, the electron configuration is the distribution of electrons of an atom or molecule (or other physical structure) in atomic or molecular orbitals. [1] For example, the electron configuration of the neon atom is 1s 2 2s 2 2p 6 , meaning that the 1s, 2s, and 2p subshells are occupied by two, two, and six ...

  9. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    Application of MO theory for dihydrogen results in having both electrons in the bonding MO with electron configuration 1σ g 2. The bond order for dihydrogen is (2-0)/2 = 1. The photoelectron spectrum of dihydrogen shows a single set of multiplets between 16 and 18 eV (electron volts). [14] The dihydrogen MO diagram helps explain how a bond breaks.