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Copper(II) chloride, also known as cupric chloride, is an inorganic compound with the chemical formula Cu Cl 2. The monoclinic yellowish-brown anhydrous form slowly absorbs moisture to form the orthorhombic blue-green dihydrate CuCl 2 ·2H 2 O , with two water molecules of hydration .
Because this reaction is highly exothermic (238 kJ/mol), the temperature is monitored, to guard against thermal degradation of the catalyst. The reaction is as follows: CH 2 =CH 2 + 2 CuCl 2 → 2 CuCl + ClH 2 C-CH 2 Cl. The copper(II) chloride is regenerated by sequential reactions of the cuprous chloride with oxygen and then hydrogen chloride:
Copper(I) chloride, commonly called cuprous chloride, is the lower chloride of copper, with the formula CuCl. The substance is a white solid sparingly soluble in water, but very soluble in concentrated hydrochloric acid .
Net reaction in the Wacker process. The Wacker process or the Hoechst-Wacker process (named after the chemical companies of the same name) refers to the oxidation of ethylene to acetaldehyde in the presence of palladium(II) chloride and copper(II) chloride as the catalyst. [1]
The Sandmeyer reaction can also be used to convert aryl amines to phenols proceeding through the formation of an aryl diazonium salt. In the presence of copper catalyst, such as copper(I) oxide, and an excess of copper(II) nitrate, this reaction takes place readily at room temperature neutral water. [28]
The mechanism of action is the insecticide binding at the GABA A site in the GABA-gated chloride channel (IRAC group 2A), which inhibits chloride flow into the nerve. [13]: 257 Other examples include dicofol, mirex, kepone, and pentachlorophenol. These can be either hydrophilic or hydrophobic, depending on their molecular structure. [14]
The formation of copper acetylide when a gas is passed through a solution of copper(I) chloride is used as a test for the presence of acetylene. Reactions between Cu + and alkynes occur only if a terminal hydrogen is present (as it is slightly acidic in nature). Thus, this reaction is used for identification of terminal alkynes.
The net reaction between an aldehyde (or an alpha-hydroxy-ketone) and the copper(II) ions in Benedict's solution may be written as: RCHO + 2 Cu 2+ + 5 OH − → RCOO − + Cu 2 O + 3 H 2 O. The hydroxide ions in the equation forms when sodium carbonate dissolves in water. With the citrate included, the reaction becomes: