enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  3. 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 .

  4. 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

  5. 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]

  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. Diphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Diphenylmethane

    The acidity of the methylene group in diphenylmethane is due to the weakness of the (C 6 H 5) 2 CH–H bond, which has a bond dissociation energy of 82 kcal mol −1 (340 kJ mol −1). [5] This is well below the published bond dissociation energies for comparable C–H bonds in propane , where BDE((CH 3 ) 2 CH–H)=98.6 kcal mol −1 , and ...

  9. 3,4,5-Trimethoxyamphetamine - Wikipedia

    en.wikipedia.org/wiki/3,4,5-trimethoxyamphetamine

    [1] [3] For comparison, mescaline is typically used at doses of 200 to 500 mg and is said to have a duration of 10 to 12 hours or longer. [4] TMA's positional isomer 2,4,5-trimethoxyamphetamine (2,4,5-TMA or TMA-2) is much more potent than TMA, with a dosage of 20 to 40 mg and a duration of 8 to 12 hours. [5]