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  2. Copper (II) chloride - Wikipedia

    en.wikipedia.org/wiki/Copper(II)_chloride

    Copper(II) chloride is used as a catalyst in a variety of processes that produce chlorine by oxychlorination. The Deacon process takes place at about 400 to 450 °C in the presence of a copper chloride: [8] 4 HCl + O 2 → 2 Cl 2 + 2 H 2 O. Copper(II) chloride catalyzes the chlorination in the production of vinyl chloride and dichloromethane. [8]

  3. List of copper salts - Wikipedia

    en.wikipedia.org/wiki/List_of_copper_salts

    Hydroxide and chloride: Copper(II) naproxen: C 28 H 26 CuO 6: naproxen: Copper(II) ibuprofenate: C 52 H 68 Cu 2 O 8: Ibuprofenate Copper(I, II) salts. Name Chemical ...

  4. Copper(I) chloride - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_chloride

    Copper(I) chloride is produced industrially by the direct combination of copper metal and chlorine at 450–900 °C: [11] [12] 2 Cu + Cl 2 → 2 CuCl. Copper(I) chloride can also be prepared by reducing copper(II) chloride with sulfur dioxide, or with ascorbic acid that acts as a reducing sugar: [13] [14]

  5. Copper(II) oxide - Wikipedia

    en.wikipedia.org/wiki/Copper(II)_oxide

    Molar mass: 79.545 g/mol ... soluble in ammonium chloride, ... Copper(II) oxide or cupric oxide is an inorganic compound with the formula CuO.

  6. Copper - Wikipedia

    en.wikipedia.org/wiki/Copper

    Many other oxyanions form complexes; these include copper(II) acetate, copper(II) nitrate, and copper(II) carbonate. Copper(II) sulfate forms a blue crystalline pentahydrate, the most familiar copper compound in the laboratory. It is used in a fungicide called the Bordeaux mixture. [67] Ball-and-stick model of the complex [Cu(NH 3) 4 (H 2 O) 2 ...

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  8. Water of crystallization - Wikipedia

    en.wikipedia.org/wiki/Water_of_crystallization

    CuSO 4 ·5H 2 O – copper(II) sulfate pentahydrate; CoCl 2 ·6H 2 O – cobalt(II) chloride hexahydrate; SnCl 2 ·2H 2 O – tin(II) (or stannous) chloride dihydrate; For many salts, the exact bonding of the water is unimportant because the water molecules are made labile upon dissolution.

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    The signal that targeting amylin could preserve lean mass during weight loss — a key question about GLP-1 drugs — has so far been from animal studies, Drucker pointed out, leading him to ...