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  2. Prism correction - Wikipedia

    en.wikipedia.org/wiki/Prism_correction

    Prism dioptres. Prism correction is commonly specified in prism dioptres, a unit of angular measurement that is loosely related to the dioptre. Prism dioptres are represented by the Greek symbol delta (Δ) in superscript. A prism of power 1 Δ would produce 1 unit of displacement for an object held 100 units from the prism. [2]

  3. Square antiprismatic molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Square_antiprismatic...

    In chemistry, the square antiprismatic molecular geometry describes the shape of compounds where eight atoms, groups of atoms, or ligands are arranged around a central atom, defining the vertices of a square antiprism. [1] This shape has D 4d symmetry and is one of the three common shapes for octacoordinate transition metal complexes, along ...

  4. Benesi–Hildebrand method - Wikipedia

    en.wikipedia.org/wiki/Benesi–Hildebrand_method

    The Benesi–Hildebrand method is a mathematical approach used in physical chemistry for the determination of the equilibrium constant K and stoichiometry of non-bonding interactions. This method has been typically applied to reaction equilibria that form one-to-one complexes, such as charge-transfer complexes and host–guest molecular ...

  5. Fine structure - Wikipedia

    en.wikipedia.org/wiki/Fine_structure

    Relativistic corrections (Dirac) to the energy levels of a hydrogen atom from Bohr's model. The fine structure correction predicts that the Lyman-alpha line (emitted in a transition from n = 2 to n = 1) must split into a doublet. The total effect can also be obtained by using the Dirac equation. In this case, the electron is treated as non ...

  6. Eyring equation - Wikipedia

    en.wikipedia.org/wiki/Eyring_equation

    Eyring equation. The Eyring equation (occasionally also known as Eyring–Polanyi equation) is an equation used in chemical kinetics to describe changes in the rate of a chemical reaction against temperature. It was developed almost simultaneously in 1935 by Henry Eyring, Meredith Gwynne Evans and Michael Polanyi.

  7. Pitzer equations - Wikipedia

    en.wikipedia.org/wiki/Pitzer_equations

    Pitzer equations [1] are important for the understanding of the behaviour of ions dissolved in natural waters such as rivers, lakes and sea-water. [2] [3] [4] They were first described by physical chemist Kenneth Pitzer. [5] The parameters of the Pitzer equations are linear combinations of parameters, of a virial expansion of the excess Gibbs ...

  8. UNIQUAC - Wikipedia

    en.wikipedia.org/wiki/UNIQUAC

    UNIQUAC. In statistical thermodynamics, UNIQUAC (a portmanteau of uni versal qua si c hemical) is an activity coefficient model used in description of phase equilibria. [1] [2] The model is a so-called lattice model and has been derived from a first order approximation of interacting molecule surfaces.

  9. Standard hydrogen electrode - Wikipedia

    en.wikipedia.org/wiki/Standard_hydrogen_electrode

    The hydrogen electrode is based on the redox half cell corresponding to the reduction of two hydrated protons, 2H+(aq), into one gaseous hydrogen molecule, H2 (g). General equation for a reduction reaction: The reaction quotient ( Qr) of the half-reaction is the ratio between the chemical activities ( a) of the reduced form (the reductant, ared ...

  10. Chemical equation - Wikipedia

    en.wikipedia.org/wiki/Chemical_equation

    A chemical equation is the symbolic representation of a chemical reaction in the form of symbols and chemical formulas.The reactant entities are given on the left-hand side and the product entities are on the right-hand side with a plus sign between the entities in both the reactants and the products, and an arrow that points towards the products to show the direction of the reaction.

  11. Edwards equation - Wikipedia

    en.wikipedia.org/wiki/Edwards_equation

    The Edwards equation in organic chemistry is a two-parameter equation for correlating nucleophilic reactivity, as defined by relative rate constants, with the basicity of the nucleophile (relative to protons) and its polarizability. This equation was first developed by John O. Edwards in 1954 [1] and later revised based on additional work in 1956.