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Organozinc compounds contain zinc—carbon covalent bonds. Diethylzinc ((C 2 H 5) 2 Zn) was first reported in 1848. It was made by reaction of zinc and ethyl iodide and is the first compound known to contain a metal—carbon sigma bond. [25] For a long time it was a mystery why copper(II) did not form an analogous compound.
Zinc chemistry resembles that of the late first-row transition metals, nickel and copper, [53] as well as certain main group elements. Almost all zinc compounds have the element in the +2 oxidation state. [54] When Zn 2+ compounds form, the outer shell s electrons are lost, yielding a bare zinc ion with the electronic configuration [Ar]3d 10. [55]
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
The key zinc-intermediate formed is a carbenoid (iodomethyl)zinc iodide which reacts with alkenes to afford the cyclopropanated product. The rate of forming the active zinc species is increased via ultrasonication since the initial reaction occurs at the surface of the metal.
Metals are insoluble in water or organic solvents, unless they undergo a reaction with them. Typically, this is an oxidation reaction that robs the metal atoms of their itinerant electrons, destroying the metallic bonding. However metals are often readily soluble in each other while retaining the metallic character of their bonding.
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Pyrometallurgy processing reduces zinc oxide with carbon or carbon monoxide at 950 °C (1,740 °F) into the metal, which is distilled as zinc vapor. [81] The zinc vapor is collected in a condenser. [80] Electrowinning processing leaches zinc from the ore concentrate by sulfuric acid. [82] After this step electrolysis is used to produce zinc ...
Metal aqua ions are often involved in the formation of complexes. The reaction may be written as pM x+ (aq) + qL y− → [M p L q] (px-qy)+ In reality this is a substitution reaction in which one or more water molecules from the first hydration shell of the metal ion are replaced by ligands, L. The complex is described as an inner-sphere complex.