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  2. Dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane

    Dichloromethane is widely used as a solvent in part because it is relatively inert. It does participate in reactions with certain strong nucleophiles however. Tert-butyllithium deprotonates DCM: [20] H 2 CCl 2 + RLi → HCCl 2 Li + RH. Methyllithium reacts with methylene chloride to give chlorocarbene: [citation needed]

  3. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    This chemical reaction is typical of alkanes and alkyl-substituted aromatics under application of UV light. The reaction is used for the industrial synthesis of chloroform (CHCl 3), dichloromethane (CH 2 Cl 2), and hexachlorobutadiene. It proceeds by a free-radical chain mechanism.

  4. Deuterated dichloromethane - Wikipedia

    en.wikipedia.org/wiki/Deuterated_dichloromethane

    Deuterated dichloromethane (CD 2 Cl 2 or C 2 H 2 Cl 2) [a] is a form (isotopologue) of dichloromethane (DCM, CH 2 Cl 2) in which the hydrogen atoms (H) are deuterium (heavy hydrogen) (2 H or D). [2] Deuterated DCM is not a common solvent used in NMR spectroscopy as it is expensive compared to deuterated chloroform .

  5. Dess–Martin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dess–Martin_oxidation

    The reaction uses a hypervalent iodine reagent [2] similar to 2-iodoxybenzoic acid to selectively and mildly oxidize alcohols to aldehydes or ketones. The reaction is commonly conducted in chlorinated solvents such as dichloromethane or chloroform. [2] The reaction can be done at room temperature and is quickly complete.

  6. Dichloromethane (data page) - Wikipedia

    en.wikipedia.org/wiki/Dichloromethane_(data_page)

    The handling of this chemical may incur notable safety precautions. ... Structure and properties ... log 10 of Dichloromethane vapor pressure.

  7. Dichlorocarbene - Wikipedia

    en.wikipedia.org/wiki/Dichlorocarbene

    Dichlorocarbene is an intermediate in the carbylamine reaction. In this conversion, a dichloromethane solution of a primary amine is treated with chloroform and aqueous sodium hydroxide in the presence of catalytic amount of the phase-transfer catalyst. Illustrative is the synthesis of tert-butyl isocyanide: [7]

  8. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2.The two compounds are isomers, each being colorless liquids with a sweet odor.

  9. 1,1-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,1-Dichloroethylene

    1,1-Dichloroethylene, commonly called vinylidene chloride or 1,1-DCE, is an organochloride with the molecular formula CCl 2 CH 2.It is a colorless liquid with a sharp odor. Like most chlorocarbons, it is poorly soluble in water but soluble in organic solvents. 1,1-DCE was the precursor to the original clingwrap, Saran, for food, but this application has been phased