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  2. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  3. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    By removing ethylene by oxidation, the permanganate delays the ripening, increasing the fruit's shelf life up to 4 weeks without the need for refrigeration. [ 52 ] [ 53 ] [ 54 ] The chemical reaction, in which ethylene (C 2 H 4 ) is oxidised by potassium permanganate (KMnO 4 ) to carbon dioxide (CO 2 ), manganese oxide (MnO 2 ) and potassium ...

  4. 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

  5. Glycerol and potassium permanganate - Wikipedia

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

    Its reaction with glycerol (commonly known as glycerin or glycerine) (C 3 H 5 (OH) 3) is highly exothermic, resulting rapidly in a flame, along with the formation of carbon dioxide and water vapour: 14 KMnO 4 (s) + 4 C 3 H 5 (OH) 3 (l) → 7 K 2 CO 3 (s) + 7 Mn 2 O 3 (s) + 5 CO 2 (g) + 16 H 2 O(g).

  6. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    Autoxidation is therefore a fairly broad term and can encompass examples of photooxygenation and catalytic oxidation. The common mechanism is a free radical chain reaction, where the addition of oxygen gives rise to hydroperoxides and their associated peroxy radicals (ROO•). [5]

  7. Chemical chameleon - Wikipedia

    en.wikipedia.org/wiki/Chemical_chameleon

    Chemical chameleon reaction. The chemical chameleon is a redox reaction, well known from classroom demonstrations, that exploits the dramatic color changes associated with the various oxidation states of manganese.

  8. Stahl oxidation - Wikipedia

    en.wikipedia.org/wiki/Stahl_oxidation

    The Stahl oxidation is a component of the undergraduate organic chemistry laboratory curriculum at UW-Madison and the University of Utah. [25] In 2013, the mechanism for the copper(I)/TEMPO oxidation of alcohols was elucidated, [24] and it was found the use of less hindered nitroxyl radical sources allowed for the oxidation of secondary ...

  9. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    Catalytic oxidation are processes that rely on catalysts to introduce oxygen into organic and inorganic compounds. Many applications, including the focus of this article, involve oxidation by oxygen. Such processes are conducted on a large scale for the remediation of pollutants, production of valuable chemicals, and the production of energy. [1]