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  2. 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. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...

  3. Meso compound - Wikipedia

    en.wikipedia.org/wiki/Meso_compound

    The two cis stereoisomers of 1,2-substituted cyclohexanes behave like meso compounds at room temperature in most cases. At room temperature, most 1,2-disubstituted cyclohexanes undergo rapid ring flipping (exceptions being rings with bulky substituents), and as a result, the two cis stereoisomers behave chemically identically with chiral ...

  4. Cis-1,2-dihydro-1,2-dihydroxynaphthalene dehydrogenase

    en.wikipedia.org/wiki/Cis-1,2-dihydro-1,2-di...

    The systematic name of this enzyme class is cis-1,2-dihydronaphthalene-1,2-diol:NAD+ 1,2-oxidoreductase. Other names in common use include (+)-cis-naphthalene dihydrodiol dehydrogenase, naphthalene dihydrodiol dehydrogenase, and cis-dihydrodiol naphthalene dehydrogenase.

  5. Cyclopentane - Wikipedia

    en.wikipedia.org/wiki/Cyclopentane

    Cyclopentane is a minor component of automobile fuel, with its share in US gasoline varying between 0.2 and 1.6% in early 1990s [8] and 0.1 to 1.7% in 2011. [9] Its research and motor octane numbers are reported as 101 or 103 and 85 or 86 respectively. [10] [11]

  6. Cis-1,2-dihydrobenzene-1,2-diol dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Cis-1,2-dihydrobenzene-1,2...

    The systematic name of this enzyme class is cis-1,2-dihydrobenzene-1,2-diol:NAD+ oxidoreductase. Other names in common use include cis-benzene glycol dehydrogenase, cis-1,2-dihydrocyclohexa-3,5-diene (nicotinamide adenine, and dinucleotide) oxidoreductase.

  7. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    Many syntheses have been developed. One popular route entails reduction of benzoin using zinc amalgam. [6]C 6 H 5 –CH(OH)–C(=O)–C 6 H 5, trans-C 6 H 5 –CH=CH–C 6 H 5. Both isomers of stilbene can be produced by decarboxylation of α-phenylcinnamic acid, trans-stilbene being produced from the (Z)-isomer of the acid.

  8. 1,2-Dichloroethane - Wikipedia

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

    The chemical compound 1,2-dichloroethane, commonly known as ethylene dichloride (EDC), is a chlorinated hydrocarbon. It is a colourless liquid with a chloroform -like odour . The most common use of 1,2-dichloroethane is in the production of vinyl chloride , which is used to make polyvinyl chloride (PVC) pipes, furniture and automobile ...

  9. trans-Cyclooctene - Wikipedia

    en.wikipedia.org/wiki/Trans-Cyclooctene

    For instance, it can be prepared in almost 100% yield by converting the cis isomer to 1,2-epoxycyclooctane ("cyclooctene oxide") followed by reactions with lithium diphenylphosphide (LiPPh 2) and with methyl iodide CH 3 I. (Similar procedures can give cis,trans isomers of 1,4-cyclooctadiene and 1,5-cyclooctadiene). [2]