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  2. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    Potassium permanganate is an inorganic compound with the chemical formula KMnO 4.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.

  3. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    A permanganate can oxidize an amine to a nitro compound, [7] [8] an alcohol to a ketone, [9] an aldehyde to a carboxylic acid, [10] [11] a terminal alkene to a carboxylic acid, [12] oxalic acid to carbon dioxide, [13] and an alkene to a diol. [14] This list is not exhaustive. In alkene oxidations one intermediate is a cyclic Mn(V) species: [15]

  4. Potassium manganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_manganate

    Potassium manganate is the inorganic compound with the formula K 2 MnO 4. This green-colored salt is an intermediate in the industrial synthesis of potassium permanganate (KMnO 4), a common chemical. [1] Occasionally, potassium manganate and potassium permanganate are confused, but each compound's properties are distinct.

  5. Chemical chameleon - Wikipedia

    en.wikipedia.org/wiki/Chemical_chameleon

    The chemical chameleon reaction shows the process in reverse, by reducing violet potassium permanganate first to green potassium manganate and eventually to brown manganese dioxide: [1] [2] [5] KMnO 4 (violet) → K 2 MnO 4 (green) → MnO 2 (brown/yellow suspension) Blue potassium hypomanganate may also form as an intermediate. [6]

  6. 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.

  7. 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.

  8. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical reaction occurs. [1] A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction. The detailed steps of a reaction are not observable in most cases.

  9. Ammonium permanganate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_permanganate

    Ammonium permanganate decomposes explosively to manganese dioxide, nitrogen, and water: [2] 2 NH 4 MnO 4 → 2 MnO 2 + N 2 + 4 H 2 O. Ammonium permanganate decomposes slowly in storage even at normal temperatures. A sample stored for 3 months was only 96% pure, after 6 months it assumed color of iodine and had strong smell of nitrogen oxides.