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Lithium cyanide is an inorganic compound with the chemical formula LiCN. It is a toxic, white coloured, hygroscopic , water-soluble salt that finds only niche uses. Preparation
Cyanide is unstable in water, but the reaction is slow until about 170 °C. It undergoes hydrolysis to give ammonia and formate, which are far less toxic than cyanide: [14] CN − + 2 H 2 O → HCO − 2 + NH 3. Cyanide hydrolase is an enzyme that catalyzes this reaction.
Pentacyanocobaltate ([Co(CN) 5] 3−) is produced by the addition of five or more equivalents of a cyanide to a solution of a cobalt(II) salt. It is square pyramidal. [ 5 ] Solutions of [Co(CN) 5 ] − 3 undergo a variety of reactions, such as hydrogenation: [ 6 ]
LiCl is removed by filtration from an ethereal solution of LAH, with subsequent precipitation of LAH to yield a product containing around 1% w/w LiCl. [10] An alternative preparation starts from LiH, and metallic Al instead of AlCl 3. Catalyzed by a small quantity of TiCl 3 (0.2%), the reaction proceeds well using dimethylether as solvent. This ...
The reaction is catalyzed by nucleophiles such as a cyanide or an N-heterocyclic carbene (usually thiazolium salts). The reaction mechanism was proposed in 1903 by A. J. Lapworth . [ 7 ] In the first step in this reaction, the cyanide anion (as sodium cyanide ) reacts with the aldehyde in a nucleophilic addition .
Solutions of metal aquo complexes are acidic owing to the ionization of protons from the water ligands. In dilute solution chromium(III) aquo complex has a pK a of about 4.3, affording a metal hydroxo complex: [Cr(H 2 O) 6] 3+ ⇌ [Cr(H 2 O) 5 (OH)] 2+ + H + Thus, the aquo ion is a weak acid, of comparable strength to acetic acid (pK a of about ...
The cyanide source can be potassium cyanide (KCN), sodium cyanide (NaCN) or trimethylsilyl cyanide ((CH 3) 3 SiCN). With aromatic aldehydes such as benzaldehyde, the benzoin condensation is a competing reaction. The reaction is used in carbohydrate chemistry as a chain extension method for example that of D-xylose.
The change of enthalpy of this reaction is equal to -481.06 kJ. [3] The heat provided by the main reaction serves as a catalyst for other side reactions. CH 4 + H 2 O → CO + 3 H 2 2 CH 4 + 3 O 2 → 2 CO + 4 H 2 O 4 NH 3 + 3 O 2 → 2 N 2 + 6 H 2 O. These side reactions can be minimized by only short exposures to the catalyst of the order of ...