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  2. Methylamine - Wikipedia

    en.wikipedia.org/wiki/Methylamine

    Methylamine has been produced industrially since the 1920s (originally by Commercial Solvents Corporation for dehairing of animal skins). [4] This was made possible by Kazimierz Smoleński [] and his wife Eugenia who discovered amination of alcohols, including methanol, on alumina or kaolin catalyst after WWI, filed two patent applications in 1919 [5] and published an article in 1921.

  3. Dimethylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylamine

    The molecule consists of a nitrogen atom with two methyl substituents and one hydrogen.Dimethylamine is a weak base and the pKa of the ammonium CH 3-NH + 2-CH 3 is 10.73, a value above methylamine (10.64) and trimethylamine (9.79).

  4. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    In chemistry, the oxidation state, or oxidation number, is the hypothetical charge of an atom if all of its bonds to other atoms were fully ionic. It describes the degree of oxidation (loss of electrons) of an atom in a chemical compound. Conceptually, the oxidation state may be positive, negative or zero. Beside nearly-pure ionic bonding, many ...

  5. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    The oxidation products derived from methyl are hydroxymethyl group −CH 2 OH, formyl group −CHO, and carboxyl group −COOH. For example, permanganate often converts a methyl group to a carboxyl (−COOH) group, e.g. the conversion of toluene to benzoic acid. Ultimately oxidation of methyl groups gives protons and carbon dioxide, as seen in ...

  6. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  7. Pinnick oxidation - Wikipedia

    en.wikipedia.org/wiki/Pinnick_Oxidation

    The Pinnick oxidation is an organic reaction by which aldehydes can be oxidized into their corresponding carboxylic acids using sodium chlorite (NaClO 2) under mild acidic conditions. It was originally developed by Lindgren and Nilsson. [ 1 ]

  8. IUPAC nomenclature of inorganic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The Roman numerals in fact show the oxidation number, but in simple ionic compounds (i.e., not metal complexes) this will always equal the ionic charge on the metal. For a simple overview see [1] Archived 2008-10-16 at the Wayback Machine , for more details see selected pages from IUPAC rules for naming inorganic compounds Archived 2016-03-03 ...

  9. Template:List of oxidation states of the elements - Wikipedia

    en.wikipedia.org/wiki/Template:List_of_oxidation...

    Element Negative states Positive states Group Notes −5 −4 −3 −2 −1 0 +1 +2 +3 +4 +5 +6 +7 +8 +9 Z; 1 hydrogen: H −1: 0 +1: 1 [1]2 helium: He 0