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  2. Potassium permanganate - Wikipedia

    en.wikipedia.org/wiki/Potassium_permanganate

    The reagent is an alkaline solution of potassium permanganate. Reaction with double or triple bonds (R 2 C=CR 2 or R−C≡C−R) causes the color to fade from purplish-pink to brown. Aldehydes and formic acid (and formates) also give a positive test. [43] The test is antiquated. Baeyer's reagent reaction

  3. 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.

  4. 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]

  5. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    The reaction is considered Markovnikov as it results in water addition with same regiospecificity as a direct hydration reaction. Alkene hydroboration-oxidation: Stereospecific: Can only be syn addition – hydrogen and hydroxyl (-OH) are added to the same face. The reaction is anti-Markovnikov. Hydroxyl attaches to the less substituted carbon.

  6. Ammonium permanganate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_permanganate

    [1] 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.

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  8. 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.

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    South Korean President Yoon Suk Yeol faces the greatest threat to his brief but chequered political career, with his fate in the hands of judges after some of his allies turned from him and voted ...