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Copper(II) bromide (Cu Br 2) is a chemical compound that forms an unstable tetrahydrate CuBr 2 ·4H 2 O. It is used in photographic processing as an intensifier and as a brominating agent in organic synthesis .
The data below tabulates standard electrode potentials (E°), in volts relative to the standard hydrogen electrode (SHE), at: . Temperature 298.15 K (25.00 °C; 77.00 °F); ...
Electrolysis of iron can eliminate direct emissions and further reduce emissions if the electricity is created from green energy. The small-scale electrolysis of iron has been successfully reported by dissolving it in molten oxide salts and using a platinum anode. [52] Oxygen anions form oxygen gas and electrons at the anode.
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]
Electrolysis is usually done in bulk using hundreds of sheets of metal connected to an electric power source. In the production of copper, these pure sheets of copper are used as starter material for the cathodes, and are then lowered into a solution such as copper sulfate with the large anodes that are cast from impure (97% pure) copper.
Usually, water is electrolysed as mentioned above in electrolysis of water yielding gaseous oxygen in the anode and gaseous hydrogen in the cathode. On the other hand, sodium chloride in water dissociates in Na + and Cl − ions. The cation, which is the positive ion, will be attracted to the cathode (−), thus reducing the sodium ion.
The exact relationship depends on the nature of the reactions at the two electrodes. For the electrolysis of aqueous copper(II) sulfate (CuSO 4) as an example, with Cu 2+ (aq) and SO 2− 4 (aq) ions, the cathode reaction is the reduction Cu 2+ (aq) + 2 e − → Cu(s) and the anode reaction is the corresponding oxidation of Cu to Cu 2+.
The Nencki reaction (1881) is the ring acetylation of phenols with acids in the presence of zinc chloride. [24] In a green chemistry variation aluminium chloride is replaced by graphite in an alkylation of p-xylene with 2-bromobutane. This variation will not work with primary halides from which less carbocation involvement is inferred. [25]