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  2. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Organochlorine chemistry is concerned with the properties of organochlorine compounds, or organochlorides, organic compounds containing at least one covalently bonded atom of chlorine. The chloroalkane class ( alkanes with one or more hydrogens substituted by chlorine) includes common examples.

  3. Category:Organochlorides - Wikipedia

    en.wikipedia.org/wiki/Category:Organochlorides

    D. Dechlorane plus; Delmadinone; Delmadinone acetate; Dense non-aqueous phase liquid; Desmethylchlorotrianisene; Deuterated chloroform; Dialifor; 1,2-Dibromo-3 ...

  4. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO.It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring (C 6 H 6) with an acyl chloride (−C(=O)Cl) substituent.

  5. Halocarbon - Wikipedia

    en.wikipedia.org/wiki/Halocarbon

    Halocarbon compounds are chemical compounds in which one or more carbon atoms are linked by covalent bonds with one or more halogen atoms (fluorine, chlorine, bromine or iodine – group 17) resulting in the formation of organofluorine compounds, organochlorine compounds, organobromine compounds, and organoiodine compounds.

  6. Dieldrin - Wikipedia

    en.wikipedia.org/wiki/Dieldrin

    It is likely that this is an example of enterohepatic recirculation, for bile contains the glucuronide. This is probably cleaved by gut microflora. There is an interesting metabolite in rat urine, first described by Klein. [13] The methylene group of the dieldrin links to one end of the ClC:CCl group to form a cage structure.

  7. Hexachloroethane - Wikipedia

    en.wikipedia.org/wiki/Hexachloroethane

    Hexachloroethane (perchloroethane) is an organochlorine compound with the chemical formula (CCl 3) 2. It is a white or colorless solid at room temperature with a camphor-like odor. [ 3 ] It has been used by the military in smoke compositions , such as base-eject smoke munitions ( smoke grenades ).

  8. Tetrachloro-m-xylene - Wikipedia

    en.wikipedia.org/wiki/Tetrachloro-m-xylene

    Tetrachloro-m-xylene (tetrachlorometaxylene, or TCMX) is the organochlorine compound with the formula C 6 Cl 4 (CH 3) 2. It is the chlorinated derivative of m-xylene in which the four aromatic hydrogen atoms are replaced by chlorine. It is prepared by ferric chloride-catalyzed reaction of the xylene with chlorine. [1]

  9. Electron configurations of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_configurations_of...

    Here [Ne] refers to the core electrons which are the same as for the element neon (Ne), the last noble gas before phosphorus in the periodic table. The valence electrons (here 3s 2 3p 3) are written explicitly for all atoms. Electron configurations of elements beyond hassium (element 108) have never been measured; predictions are used below.