enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. List of isomers of tridecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tridecane

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    If one of the methyl groups attached to the third carbon atom were instead an ethyl group, then the name would be 3-ethyl-2,3-dimethylpentane. When there are different alkyl groups, they are listed in alphabetical order.

  4. 2-Phenylhexane - Wikipedia

    en.wikipedia.org/wiki/2-Phenylhexane

    2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene ., [ 1 ] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride , [ 2 ] scandium(III) triflate , [ 3 ] and phosphoric acid .

  5. Gutmann–Beckett method - Wikipedia

    en.wikipedia.org/wiki/Gutmann–Beckett_method

    Gutmann, a chemist renowned for his work on non-aqueous solvents, described an acceptor-number scale for solvent Lewis acidity [4] with two reference points relating to the 31 P NMR chemical shift of Et 3 PO in the weakly Lewis acidic solvent hexane (δ = 41.0 ppm, AN 0) and in the strongly Lewis acidic solvent SbCl 5 (δ = 86.1 ppm, AN 100).

  6. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

  7. List of isomers of dodecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_dodecane

    The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.

  8. Structural scheduling of synthetic cannabinoids - Wikipedia

    en.wikipedia.org/wiki/Structural_scheduling_of...

    Naphthoylindoles: Any compound containing a 3-(1-naphthoyl)indole structure with substitution at the nitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or 2-(4-morpholinyl)ethyl group, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any ...

  9. 3-Ethylpentane - Wikipedia

    en.wikipedia.org/wiki/3-ethylpentane

    3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]