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Copper nitrate, in combination with acetic anhydride, is an effective reagent for nitration of aromatic compounds, known as the Menke nitration. [17] Hydrated copper nitrate adsorbed onto clay affords a reagent called "Claycop". The resulting blue-colored clay is used as a slurry, for example for the oxidation of thiols to disulfides.
Hydroxide is a diatomic anion with chemical formula OH −. It consists of an oxygen and hydrogen atom held together by a single covalent bond, and carries a negative electric charge. It is an important but usually minor constituent of water. It functions as a base, a ligand, a nucleophile, and a catalyst.
Given nitrate's low basicity, the tendency of metal nitrate complexes toward hydrolysis is expected. Thus copper(II) nitrate readily dissociates in aqueous solution to give the aqua complex: Cu(NO 3) 2 + 6 H 2 O → [Cu(H 2 O) 6](NO 3) 2. Pyrolysis of metal nitrates yields oxides. [18] Ni(NO 3) 2 → NiO + NO 2 + 0.5 O 2
Hydrotalcite (white) and yellow-green serpentine, Snarum, Modum, Buskerud, Norway.Size: 8.4 × 5.2 × 4.1 cm. Layered double hydroxides (LDH) are a class of ionic solids characterized by a layered structure with the generic layer sequence [AcB Z AcB] n, where c represents layers of metal cations, A and B are layers of hydroxide (OH −
They are very reactive towards oxygen to form copper(I) oxide and have many uses in chemistry. They are synthesized by treating copper(I) compounds with Grignard reagents , terminal alkynes or organolithium reagents ; [ 12 ] in particular, the last reaction described produces a Gilman reagent .
It can be formed by heating copper in air at around 300–800 °C: 2 Cu + O 2 → 2 CuO. For laboratory uses, copper(II) oxide is conveniently prepared by pyrolysis of copper(II) nitrate or basic copper(II) carbonate: [4] 2 Cu(NO 3) 2 → 2 CuO + 4 NO 2 + O 2 (180°C) Cu 2 (OH) 2 CO 3 → 2 CuO + CO 2 + H 2 O. Dehydration of cupric hydroxide ...
However, the hydrogen bonding in NH 3 is weaker than that in H 2 O due to the lower electronegativity of nitrogen compared to oxygen and the presence of only one lone pair in NH 3 rather than two in H 2 O. It is a weak base in aqueous solution (pK b 4.74); its conjugate acid is ammonium, NH + 4.
δ-Bi 2 O 3 has a defective fluorite-type crystal structure in which two of the eight oxygen sites in the unit cell are vacant. [5] ε-Bi 2 O 3 has a structure related to the α- and β- phases but as the structure is fully ordered it is an ionic insulator. It can be prepared by hydrothermal means and transforms to the α- phase at 400 °C.