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  2. Latimer diagram - Wikipedia

    en.wikipedia.org/wiki/Latimer_diagram

    In a Latimer diagram, because by convention redox reactions are shown in the direction of reduction (gain of electrons), the most highly oxidized form of the element is on the left side, with successively lower oxidation states to the right side. The species are connected by arrows, and the numerical value of the standard potential (in volts ...

  3. Leclanché cell - Wikipedia

    en.wikipedia.org/wiki/Leclanché_cell

    A 1919 illustration of a Leclanché cell. The Leclanché cell is a battery invented and patented by the French scientist Georges Leclanché in 1866. [1] [2] [3] The battery contained a conducting solution (electrolyte) of ammonium chloride, a cathode (positive terminal) of carbon, a depolarizer of manganese dioxide (oxidizer), and an anode (negative terminal) of zinc (reductant).

  4. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Redox (/ ˈrɛdɒks / RED-oks, / ˈriːdɒks / REE-doks, reduction–oxidation[2] or oxidation–reduction[3]: 150 ) is a type of chemical reaction in which the oxidation states of the reactants change. [4] Oxidation is the loss of electrons or an increase in the oxidation state, while reduction is the gain of electrons or a decrease in the ...

  5. Elbs persulfate oxidation - Wikipedia

    en.wikipedia.org/wiki/Elbs_persulfate_oxidation

    RSC ontology ID. RXNO:0000179. The Elbs persulfate oxidation is the organic reaction of phenols with alkaline potassium persulfate to form para -diphenols. [1] The reaction is generally performed in water at room temperatures or below, using equimolar quantities of reagents. Several reviews have been published. [2][3][4]

  6. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The Wolff–Kishner reduction is a reaction used in organic chemistry to convert carbonyl functionalities into methylene groups. [1][2] In the context of complex molecule synthesis, it is most frequently employed to remove a carbonyl group after it has served its synthetic purpose of activating an intermediate in a preceding step.

  7. Stephen aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Stephen_aldehyde_synthesis

    Organic redox reaction. Stephen aldehyde synthesis, a named reaction in chemistry, was invented by Henry Stephen (OBE / MBE). This reaction involves the preparation of aldehydes (R-CHO) from nitriles (R-CN) using tin (II) chloride (SnCl 2), hydrochloric acid (HCl) and quenching the resulting iminium salt ( [R-CH=NH 2] + Cl −) with water (H 2 ...

  8. 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 ...

  9. Redox indicator - Wikipedia

    en.wikipedia.org/wiki/Redox_indicator

    Redox indicator. A redox indicator (also called an oxidation-reduction indicator) is an indicator which undergoes a definite color change at a specific electrode potential. The requirement for fast and reversible color change means that the oxidation-reduction equilibrium for an indicator redox system needs to be established very quickly.