enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Condensation of Methyl propionate with formaldehyde followed by dehydration yields methyl methacrylate: [4]. MeO 2 CCH 2 CH 3 + CH 2 O → MeO 2 CCH(CH 2 OH)CH 3 MeO 2 CCH(CH 2 OH)CH 3 → MeO 2 CC(=CH 2)CH 3

  3. Methoxyethane - Wikipedia

    en.wikipedia.org/wiki/Methoxyethane

    Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3.Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications.

  4. Ethyl propionate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_propionate

    This article about an ester is a stub. You can help Wikipedia by expanding it.

  5. Diethyl ether - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether

    Most diethyl ether is produced as a byproduct of the vapor-phase hydration of ethylene to make ethanol.This process uses solid-supported phosphoric acid catalysts and can be adjusted to make more ether if the need arises: [9] Vapor-phase dehydration of ethanol over some alumina catalysts can give diethyl ether yields of up to 95%.

  6. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    Carboxylic acids are organic acids characterized by a carboxyl (-COOH) functional group. The naming of these compounds is governed by IUPAC nomenclature, which ensures systematic and consistent naming of chemicals.

  7. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    The Kolbe electrolysis or Kolbe reaction is an organic reaction named after Hermann Kolbe. [1] The Kolbe reaction is formally a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions).

  8. Diethyl ether (data page) - Wikipedia

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

    Phase behavior Triple point: 156.92 K (–116.23 °C), ? Pa Critical point: 467 K (194 °C), 3600 kPa Std enthalpy change of fusion, Δ fus H o: 7.19 kJ/mol Std entropy change

  9. Acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Acid_catalysis

    Acid catalysis is mainly used for organic chemical reactions. Many acids can function as sources for the protons. Acid used for acid catalysis include hydrofluoric acid (in the alkylation process), phosphoric acid, toluenesulfonic acid, polystyrene sulfonate, heteropoly acids, zeolites.