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  2. Manganese(II) acetate - Wikipedia

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

    173.027 g/mol (anhydrous) 245.087 g/mol (tetrahydrate) Appearance white crystals (anhydrous) light pink monoclinic crystals (tetrahydrate) Density: 1.74 g/cm 3 (anhydrous) 1.59 g/cm 3 (tetrahydrate) Melting point: 210 °C (410 °F; 483 K) (anhydrous) 80 °C (tetrahydrate) Solubility: soluble in water (about 700g/L at 20°C for tetrahydrate ...

  3. Manganese (III) acetate - Wikipedia

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

    Manganese triacetate has been used as a one-electron oxidant.It can oxidize alkenes via addition of acetic acid to form lactones. [3]This process is thought to proceed via the formation of a •CH 2 CO 2 H radical intermediate, which then reacts with the alkene, followed by additional oxidation steps and finally ring closure. [1]

  4. Heats of vaporization of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Heats_of_vaporization_of...

    J.A. Dean (ed.), Lange's Handbook of Chemistry (15th Edition), McGraw-Hill, 1999; Section 6, Thermodynamic Properties; Table 6.4, Heats of Fusion, Vaporization, and Sublimation and Specific Heat at Various Temperatures of the Elements and Inorganic Compounds

  5. Nickel(II) acetate - Wikipedia

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

    The compound can be prepared by treating nickel or nickel(II) carbonate with acetic acid: . NiCO 3 + 2 CH 3 CO 2 H + 3 H 2 O → Ni(CH 3 CO 2) 2 ·4 H 2 O + CO 2. The mint-green tetrahydrate has been shown by X-ray crystallography to adopt an octahedral structure, the central nickel centre being coordinated by four water molecules and two acetate ligands. [5]

  6. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    In organic chemistry, the acetoxy group (abbr. AcO or OAc; IUPAC name: acetyloxy [1]), is a functional group with the formula −OCOCH 3 and the structure −O−C(=O)−CH 3. As the -oxy suffix implies, it differs from the acetyl group (−C(=O)−CH 3) by the presence of an additional oxygen atom. The name acetoxy is the short form of acetyl-oxy.

  7. 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.

  8. Enthalpy change of solution - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_change_of_solution

    Enthalpy change of solution in water at 25 °C for some selected compounds [2] Compound ΔH o in kJ/mol; hydrochloric acid: −74.84 ammonium nitrate +25.69 ammonia: −30.50 potassium hydroxide: −57.61 caesium hydroxide: −71.55 sodium chloride +3.87 potassium chlorate +41.38 acetic acid: −1.51 sodium hydroxide: −44.50

  9. Magnesium acetate - Wikipedia

    en.wikipedia.org/wiki/Magnesium_acetate

    2 CH 3 COOH + Mg(OH) 2 → (CH 3 COO) 2 Mg + 2 H 2 O. Magnesium carbonate suspended in distilled water with 20% acetic acid solution. [8] 2 CH 3 COOH + MgCO 3 → Mg(CH 3 COO) 2 + CO 2 + H 2 O. Reacting metallic magnesium with acetic acid dissolved in dry benzene causes magnesium acetate to form along with the release of hydrogen gas. [9] Mg ...

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