enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    The actual physiological potential depends on the ratio of the reduced (Red) and oxidized (Ox) forms according to the Nernst equation and the thermal voltage. When an oxidizer (Ox) accepts a number z of electrons ( e −) to be converted in its reduced form (Red), the half-reaction is expressed as: Ox + z e − → Red

  3. Reduction potential - Wikipedia

    en.wikipedia.org/wiki/Reduction_potential

    In aqueous solutions, redox potential is a measure of the tendency of the solution to either gain or lose electrons in a reaction. A solution with a higher (more positive) reduction potential than some other molecule will have a tendency to gain electrons from this molecule (i.e. to be reduced by oxidizing this other molecule) and a solution with a lower (more negative) reduction potential ...

  4. Nernst equation - Wikipedia

    en.wikipedia.org/wiki/Nernst_equation

    In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...

  5. Frost diagram - Wikipedia

    en.wikipedia.org/wiki/Frost_diagram

    The pH dependence is given by the factor −0.059m/n per pH unit, where m relates to the number of protons in the equation, and n the number of electrons exchanged. Electrons are always exchanged in electrochemistry, but not necessarily protons. If there is no proton exchange in the reaction equilibrium, the reaction is said to be pH-independent.

  6. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    Both the oxidation and reduction steps are pH dependent. Figure 1 shows the standard potentials at pH 0 (strongly acidic) as referenced to the normal hydrogen electrode (NHE). 2 half reactions (at pH = 0) Oxidation 2H 2 O → 4H + + 4e − + O 2 E° = +1.23 V vs. NHE Reduction 4H + + 4e − → 2H 2 E° = 0.00 V vs. NHE

  7. Equivalence point - Wikipedia

    en.wikipedia.org/wiki/Equivalence_point

    The equivalence point, or stoichiometric point, of a chemical reaction is the point at which chemically equivalent quantities of reactants have been mixed. For an acid-base reaction the equivalence point is where the moles of acid and the moles of base would neutralize each other according to the chemical reaction.

  8. Enthalpy of neutralization - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_of_neutralization

    In chemistry and thermodynamics, the enthalpy of neutralization (ΔH n) is the change in enthalpy that occurs when one equivalent of an acid and a base undergo a neutralization reaction to form water and a salt. It is a special case of the enthalpy of reaction. It is defined as the energy released with the formation of 1 mole of water.

  9. Standard hydrogen electrode - Wikipedia

    en.wikipedia.org/wiki/Standard_hydrogen_electrode

    During the early development of electrochemistry, researchers used the normal hydrogen electrode as their standard for zero potential. This was convenient because it could actually be constructed by "[immersing] a platinum electrode into a solution of 1 N strong acid and [bubbling] hydrogen gas through the solution at about 1 atm pressure".