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  2. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Stages in the oxidation of primary alcohols to carboxylic acids via aldehydes and aldehyde hydrates. Almost all industrial scale oxidations use oxygen or air as the oxidant. [2] Through a variety of mechanisms, the removal of a hydride equivalent converts a primary or secondary alcohol to an aldehyde or ketone, respectively.

  3. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    It is a purplish-black crystalline salt, which dissolves in water as K + and MnO − 4 ions to give an intensely pink to purple solution. Potassium permanganate is widely used in the chemical industry and laboratories as a strong oxidizing agent , and also as a medication for dermatitis , for cleaning wounds , and general disinfection .

  4. Glycerol and potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Glycerol_and_potassium...

    The white smoke-like vapor produced by the reaction is a mixture of carbon dioxide gas and water vapor. Since the reaction is highly exothermic, initial sparking occurs, followed by a lilac- or pink-colored flame. [9] When energy or heat is added to electrons, their energy level increases to an excited state.

  5. Alcohol (chemistry) - Wikipedia

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

    Formation of a secondary alcohol via alkene reduction and hydration is shown: The hydroboration-oxidation and oxymercuration-reduction of alkenes are more reliable in organic synthesis. Alkenes react with N-bromosuccinimide and water in halohydrin formation reaction. Amines can be converted to diazonium salts, which are then hydrolyzed.

  6. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    In an acidic solution, permanganate(VII) is reduced to the pale pink manganese(II) (Mn 2+) with an oxidation state of +2. 8 H + + MnO − 4 + 5 e − → Mn 2+ + 4 H 2 O. In a strongly basic or alkaline solution, permanganate(VII) is reduced to the green manganate ion, MnO 2− 4 with an oxidation state of +6. MnO − 4 + e − → MnO 2− 4

  7. Shilov system - Wikipedia

    en.wikipedia.org/wiki/Shilov_system

    Shilov cycle The overall charge is omitted from the complexes since the exact coordination sphere of the active species is unknown. The Shilov system is a classic example of catalytic C-H bond activation and oxidation which preferentially activates stronger C-H bonds over weaker C-H bonds for an overall partial oxidation.

  8. Oxygen-evolving complex - Wikipedia

    en.wikipedia.org/wiki/Oxygen-evolving_complex

    The mechanism for splitting water involves absorption of three photons before the fourth provides sufficient energy for water oxidation. [4] Based on a widely accepted theory from 1970 by Kok, the complex can exist in 5 states, denoted S 0 to S 4 , with S 0 the most reduced and S 4 the most oxidized.

  9. Mukaiyama hydration - Wikipedia

    en.wikipedia.org/wiki/Mukaiyama_hydration

    Studies investigating the mechanism of cobalt-catalyzed peroxidation of alkenes by Nojima and coworkers, [4] support the intermediacy of a metal hydride that reacts with the alkene directly to form a transient cobalt-alkyl bond. Homolysis generates a carbon centered radical that reacts directly with oxygen and is subsequently trapped by a ...