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  2. Manganese(II) sulfate - Wikipedia

    en.wikipedia.org/wiki/Manganese(II)_sulfate

    mno 2 + so 2 + h 2 o → mnso 4 (h 2 o) It can also be made by mixing potassium permanganate with sodium hydrogen sulfate and hydrogen peroxide . Manganese sulfate is a by-product of various industrially significant oxidations that use manganese dioxide, including the manufacture of hydroquinone and anisaldehyde .

  3. Swern oxidation - Wikipedia

    en.wikipedia.org/wiki/Swern_oxidation

    The reaction conditions allow oxidation of acid-sensitive compounds, which might decompose under the acidic oxidation conditions such as Jones oxidation. For example, in Thompson & Heathcock's synthesis of the sesquiterpene isovelleral, [ 15 ] the final step uses the Swern protocol, avoiding rearrangement of the acid-sensitive ...

  4. Pinnick oxidation - Wikipedia

    en.wikipedia.org/wiki/Pinnick_Oxidation

    Chlorine dioxide reacts rapidly with H 2 O 2 to form chlorous acid. 2ClO 2 + H 2 O 2 → 2HClO 2 + O 2. Also the formation of oxygen gives good indication of the progress of the reaction. However, problems sometimes arise due to the formation of singlet oxygen in this reaction, which may oxidize organic materials (i.e. the Schenck ene reaction).

  5. Manganese-mediated coupling reactions - Wikipedia

    en.wikipedia.org/wiki/Manganese-mediated...

    The outcomes of manganese-mediated coupling reactions depend on both the structure of the substrate(s) and the reaction conditions. This section describes the scope and limitations of inter- and intramolecular manganese-mediated radical coupling reactions and is organized according to the carbonyl compound employed as the substrate.

  6. Manganese - Wikipedia

    en.wikipedia.org/wiki/Manganese

    In Mn(CH 3) 2 (dmpe) 2, Mn(II) is low spin, which contrasts with the high spin character of its precursor, MnBr 2 (dmpe) 2 (dmpe = (CH 3) 2 PCH 2 CH 2 P(CH 3) 2). [38] Polyalkyl and polyaryl derivatives of manganese often exist in higher oxidation states, reflecting the electron-releasing properties of alkyl and aryl ligands.

  7. Permanganate - Wikipedia

    en.wikipedia.org/wiki/Permanganate

    2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2 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 ]

  8. Manganese(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Manganese(II)_acetate

    The anhydrous material and dihydrate Mn(CH 3 CO 2) 2 ·2H 2 O are coordination polymers. The dihydrate has been characterized by X-ray crystallography. Each Mn(II) center is surrounded by six oxygen centers provided by aquo ligands and acetates. Subunit of the structure of the dihydrate of manganese(II) acetate. [5]

  9. Manganese peroxidase - Wikipedia

    en.wikipedia.org/wiki/Manganese_peroxidase

    The 3 substrates of this enzyme are Mn(II), H +, and H 2 O 2, whereas its two products are Mn(III) and H 2 O. This enzyme belongs to the family of oxidoreductases, to be specific those acting on a peroxide as acceptor (peroxidases). The systematic name of this enzyme class is Mn(II):hydrogen-peroxide oxidoreductase.