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  2. Chloroethane - Wikipedia

    en.wikipedia.org/wiki/Chloroethane

    Chloroethane, commonly known as ethyl chloride, is a chemical compound with chemical formula CH 3 CH 2 Cl, once widely used in producing tetraethyllead, a gasoline additive. It is a colorless, flammable gas or refrigerated liquid with a faintly sweet odor.

  3. Proton nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Proton_nuclear_magnetic...

    Simple molecules have simple spectra. The spectrum of ethyl chloride consists of a triplet at 1.5 ppm and a quartet at 3.5 ppm in a 3:2 ratio. The spectrum of benzene consists of a single peak at 7.2 ppm due to the diamagnetic ring current. Together with carbon-13 NMR, proton NMR is a powerful tool for molecular structure characterization.

  4. 1,2-Dichloroethane (data page) - Wikipedia

    en.wikipedia.org/wiki/1,2-Dichloroethane_(data_page)

    Proton NMR Carbon-13 NMR Other NMR data MS; Masses of main fragments This ...

  5. Tetraethylammonium chloride - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_chloride

    Tetraethylammonium chloride (TEAC) is a quaternary ammonium compound with the chemical formula [N(CH 2 CH 3) 4] + Cl −, sometimes written as [NEt 4]Cl. In appearance, it is a hygroscopic, colorless, crystalline solid.

  6. Trimethylsilyl group - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_group

    Also compounds, such as high temperature silicone "stopcock" grease, which have polysiloxanes (often called silicones) in them will commonly show peaks from their methyl groups (attached to the silicon atoms) having NMR chemical shifts close to the tetramethylsilane standard peak, such as at 0.07 ppm in CDCl 3.

  7. Ethylaluminium sesquichloride - Wikipedia

    en.wikipedia.org/wiki/Ethylaluminium_sesquichloride

    Methyl, ethyl, and other alkyl or aralkyl halides that are not dehydrohalogenated readily can react with aluminium in an exothermic process to form organoaluminium sesquihalides in high yields. An important example is the reaction of ethyl chloride with aluminium to form ethylaluminium sesquichloride. 3 C 2 H 5 Cl + 2 Al → (C 2 H 5) 3 Al 2 Cl 3

  8. 1,2-Dichloroethane - Wikipedia

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

    In the laboratory it is occasionally used as a source of chlorine, with elimination of ethene and chloride. Via several steps, 1,2-dichloroethane is a precursor to 1,1,1-trichloroethane . Historically, before leaded petrol was phased out, chloroethanes were used as an additive in petrol to prevent lead buildup in engines.

  9. Ethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_chloroformate

    Ethyl chloroformate is an organic compound with the chemical formula ClCO 2 CH 2 CH 3. It is the ethyl ester of chloroformic acid. It is a colorless, corrosive and highly toxic liquid. It is a reagent used in organic synthesis for the introduction of the ethyl carbamate protecting group [3] and for the formation of carboxylic anhydrides.