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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.
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.
Zinc is a strong reducing agent with a standard redox potential of −0.76 V. Pure zinc tarnishes rapidly in air, rapidly forming a passive layer. The composition of this layer can be complex, but one constituent is probably basic zinc carbonate, Zn 5 (OH) 6 CO 3. [8] The reaction of zinc with water is slowed by this passive layer.
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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]
Magnesium has a mild reaction with cold water. The reaction is short-lived because the magnesium hydroxide layer formed on the magnesium is almost insoluble in water and prevents further reaction. Mg(s) + 2H 2 O(l) Mg(OH) 2 (s) + H 2 (g) [11] A metal reacting with cold water will produce a metal hydroxide and hydrogen gas.
As a result, zinc and cadmium metal are good reducing agents. The elements of group 12 have an oxidation state of +2 in which the ions have the rather stable d 10 electronic configuration, with a full sub-shell. However, mercury can easily be reduced to the +1 oxidation state; usually, as in the ion Hg 2+
According to the Association of American Feed Control Officials (AAFCO), a metal–amino acid chelate is defined as the product resulting from the reaction of metal ions from a soluble metal salt with amino acids, with a mole ratio in the range of 1–3 (preferably 2) moles of amino acids for one mole of metal.