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  2. Copper(I) iodide - Wikipedia

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

    Copper(I) iodide reacts with mercury vapors to form brown copper(I) tetraiodomercurate(II): 4 CuI + Hg → (Cu +) 2 [HgI 4] 2− + 2 Cu. This reaction can be used for the detection of mercury since the white CuI to brown Cu 2 [HgI 4] color change is dramatic. Copper(I) iodide is used in the synthesis of Cu(I) clusters such as [Cu 6 I 7] −. [10]

  3. List of copper salts - Wikipedia

    en.wikipedia.org/wiki/List_of_copper_salts

    Copper is a chemical element with the symbol Cu (from Latin: cuprum) and the atomic number of 29. It is easily recognisable, due to its distinct red-orange color.Copper also has a range of different organic and inorganic salts, having varying oxidation states ranging from (0,I) to (III).

  4. Iodometry - Wikipedia

    en.wikipedia.org/wiki/Iodometry

    Iodometry is commonly employed to determine the active amount of hypochlorite in bleach responsible for the bleaching action. In this method, excess but known amount of iodide is added to known volume of sample, in which only the active (electrophilic) can oxidize iodide to iodine. The iodine content and thus the active chlorine content can be ...

  5. Phenylcopper - Wikipedia

    en.wikipedia.org/wiki/Phenylcopper

    Phenylcopper was the first known organocopper compound and was first prepared in 1923 from phenylmagnesium iodide and copper(I) iodide and in 1936 by Henry Gilman by transmetallation of phenylmagnesium iodide with copper(I) chloride. Phenylcopper can be obtained by reacting phenyl lithium with copper(I) bromide in diethyl ether. [3]

  6. Tetrakis(acetonitrile)copper(I) tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(acetonitrile...

    Tetrakis(acetonitrile)copper(I) tetrafluoroborate can be prepared starting from nitrosyl tetrafluoroborate, which is obtained from dinitrogen tetroxide and tetrafluoroboric acid. The nitrosyl salt is then reacted with metallic copper in acetonitrile, initially producing a green-blue copper(II) complex. This complex is reduced to the copper(I ...

  7. Finkelstein reaction - Wikipedia

    en.wikipedia.org/wiki/Finkelstein_reaction

    The aromatic chlorides and bromides are not easily substituted by iodide, though they may occur when appropriately catalyzed. The so-called "aromatic Finkelstein reaction" is catalyzed by copper(I) iodide in combination with diamine ligands. [9] Nickel bromide and tri-n-butylphosphine have been found to be suitable catalysts as well. [10]

  8. Copper(I) oxide - Wikipedia

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

    Pourbaix diagram for copper in uncomplexed media (anions other than OH − not considered). Ion concentration 0.001 mol/kg water. Temperature 25 °C. Formation of copper(I) oxide is the basis of the Fehling's test and Benedict's test for reducing sugars. These sugars reduce an alkaline solution of a copper(II) salt, giving a bright red ...

  9. Copper compounds - Wikipedia

    en.wikipedia.org/wiki/Copper_compounds

    Some copper proteins form oxo complexes, which also feature copper(III). [20] With tetrapeptides, purple-colored copper(III) complexes are stabilized by the deprotonated amide ligands. [21] Complexes of copper(III) are also found as intermediates in reactions of organocopper compounds. [22] For example, in the Kharasch–Sosnovsky reaction.