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Zinc nitrate is usually prepared by dissolving zinc metal, zinc oxide, or related materials in nitric acid: Zn + 2 HNO 3 → Zn(NO 3) 2 + H 2 ZnO + 2 HNO 3 → Zn(NO 3) 2 + H 2 O. These reactions are accompanied by the hydration of the zinc nitrate. The anhydrous salt arises by the reaction of anhydrous zinc chloride with nitrogen dioxide: [1]
Zinc nitride reacts violently with water to form ammonia and zinc oxide. [3] [4] Zn 3 N 2 + 3 H 2 O → 3 ZnO + 2 NH 3. Zinc nitride reacts with lithium (produced in an electrochemical cell) by insertion. The initial reaction is the irreversible conversion into LiZn in a matrix of beta-Li 3 N. These products then can be converted reversibly and ...
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.
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.
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.
Liquid water and ice, for example, form a frigorific mixture at 0 °C or 32 °F. This mixture was once used to define 0 °C. That temperature is now defined as the triple point of Water with well-defined isotope ratios. A mixture of ammonium chloride, water, and ice form a
The Reformatsky reaction (sometimes transliterated as Reformatskii reaction) is an organic reaction which condenses aldehydes or ketones with α-halo esters using metallic zinc to form β-hydroxy-esters: [1] [2] The Reformatsky reaction. The organozinc reagent, also called a 'Reformatsky enolate', is prepared by treating an alpha-halo ester ...
The reaction produces a primary, secondary, or tertiary alcohol via a 1,2-addition. The Barbier reaction is advantageous because it is a one-pot process: the organozinc reagent is generated in the presence of the carbonyl substrate. Organozinc reagents are also less water sensitive, thus this reaction can be conducted in water.