- hydrocyanation
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Any reaction in which the elements of hydrogen cyanide are added to a molecule, especially across a double bond
Wikipedia foundation.
Wikipedia foundation.
Hydrocyanation — is, most fundamentally, the process whereby H+ and ndash;CN ions are added to a molecular substrate. Usually the substrate is an alkene and the product is a nitrile. When ndash;CN is a ligand in a transition metal complex, its basicity makes it… … Wikipedia
Adiponitrile — IUPAC name Hexanedinitrile … Wikipedia
Bite angle — Chelate bite angle is a geometric parameter used to classify chelating ligands in inorganic and organometallic chemistry. Together with ligand cone angle, this parameter is relevant to diphosphine ligands, which are used in industrial processes… … Wikipedia
Diethylaluminium cyanide — IUPAC name diethylalumanylformonitrile … Wikipedia
Nitrile — This article is about the group of organic compounds. For the synthetic rubber product, see Nitrile rubber. The structure of the nitrile group A nitrile is any organic compound that has a C≡N functional group.[1] … Wikipedia
Triptycene — Chembox new Name = Triptycene ImageFileL1 = Triptycene.png ImageSizeL1 = 120px ImageNameL1 = triptycene ImageFileR1 = Triptycene3D.png ImageSizeR1 = 150px Section1 = Chembox Identifiers CASOther = 477 75 8 SMILES = C12=CC=CC=C1C3C5=C… … Wikipedia
Cyanide — This article is about the class of chemical compounds. For other uses, see Cyanide (disambiguation). The cyanide ion, CN−. From the top: 1. Valence bond structure 2. Space filling model 3. Electrostatic potential surface 4. Carbon lone pair… … Wikipedia
Hydrogen cyanide — IUPAC name … Wikipedia
1,3-Butadiene — Divinyl redirects here. For the band, see Divinyls. 1,3 Butadiene … Wikipedia
Asymmetric synthesis — Asymmetric synthesis, also called chiral synthesis, enantioselective synthesis or stereoselective synthesis, is organic synthesis which introduces one or more new and desired elements of chirality. [GoldBookRef|title=asymmetric synthesis| file =… … Wikipedia