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Fluorine's chemistry includes inorganic compounds formed with hydrogen, metals, nonmetals, and even noble gases; as well as a diverse set of organic compounds. [note 1] For many elements (but not all) the highest known oxidation state can be achieved in a fluoride. For some elements this is achieved exclusively in a fluoride, for others ...
List of inorganic compounds. ... (only simple oxides, oxyhalides, and related compounds, not hydroxides, carbonates, acids, or other compounds listed elsewhere) P
The Inorganic Crystal Structure Database (ICSD) in its definition of "inorganic" carbon compounds, states that such compounds may contain either C-H or C-C bonds, but not both. [7] The book series Inorganic Syntheses does not define inorganic compounds. The majority of its content deals with metal complexes of organic ligands.
The structure of the molecule of urea is O=C(−NH 2) 2.The urea molecule is planar when in a solid crystal because of sp 2 hybridization of the N orbitals. [8] [9] It is non-planar with C 2 symmetry when in the gas phase [10] or in aqueous solution, [9] with C–N–H and H–N–H bond angles that are intermediate between the trigonal planar angle of 120° and the tetrahedral angle of 109.5°.
The interhalogens of form XY have physical properties intermediate between those of the two parent halogens. The covalent bond between the two atoms has some ionic character, the less electronegative halogen, X, being oxidised and having a partial positive charge.
Maltose (/ ˈ m ɔː l t oʊ s / [2] or / ˈ m ɔː l t oʊ z / [3]), also known as maltobiose or malt sugar, is a disaccharide formed from two units of glucose joined with an α(1→4) bond. In the isomer isomaltose , the two glucose molecules are joined with an α(1→6) bond.
A group of international researchers has discovered a previously unknown chemical compound in U.S. drinking water — and it could be toxic.. The compound — known as chloronitramide anion — is ...
However, inorganic compounds featuring unsaturation in the form of triple bonds may be denoted by substitutive nomenclature with the same methods used with alkynes (i.e. the name of the corresponding saturated compound is modified by replacing the "-ane" ending with "-yne"). "-diyne" is used when there are two triple bonds, and so on.