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Several other crystalline forms of CuCl appear at high pressures several GPa. The same hydrochloric acid solutions also react with acetylene gas to form [CuCl C2H2 ]. Alkene complexes o can be prepared by reduction of CuCl2 by sulfur dioxide in the presence of the alkene in alcohol solution. Its affinity for carbon monoxide in the presence of aluminium chloride is exploited in the COPureSM process. In organic synthesis[ edit ] CuCl is used with carbon monoxide , aluminium chloride , and hydrogen chloride in the Gatterman-Koch reaction to form benzaldehydes. In the Sandmeyer reaction. Early investigators observed that copper I halides catalyse 1,4-addition of Grignard reagents to alpha,beta-unsaturated ketones [19] led to the development of organocuprate reagents that are widely used today in organic synthesis : [20] This finding led to the development of organocopper chemistry. Grignard reagents form similar organocopper compounds. Although other copper I compounds such as copper I iodide are now more often used for these types of reactions, copper I chloride is still recommended in some cases: [21] Here, Bu indicates an n- butyl group. Copper/Red Stuff/Chemical Reaction. Copper/Red Stuff/Chemical Reaction

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Copper/Red Stuff/Chemical Reaction

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Copper/Red Stuff/Chemical Reaction

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Copper/Red Stuff/Chemical Reaction

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