enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Propylene oxide - Wikipedia

    en.wikipedia.org/wiki/Propylene_oxide

    Grignard reagents add to propylene oxide to give secondary alcohols. Some other reactions of propylene oxide include: [14] Reaction with aluminium oxide at 250–260 °C leads to propionaldehyde and a little acetone. Reaction with silver(I) oxide leads to acetic acid. Reaction with sodium–mercury amalgam and water leads to isopropanol.

  3. Alkoxylation - Wikipedia

    en.wikipedia.org/wiki/Alkoxylation

    Alkoxylation is a chemical reaction that involves the addition of an epoxide to another compound. The usual manifestation of this reaction is ethoxylation of alcohols (ROH), in which case ethylene oxide is the alkoxylating agent: ROH + C 2 H 4 O → ROCH 2 CH 2 OH. Another industrially significant epoxide is propylene oxide (PO, OCH 2 CHCH 3 ...

  4. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    The common mechanism is a free radical chain reaction, where the addition of oxygen gives rise to hydroperoxides and their associated peroxy radicals (ROO•). [5] Typically, an induction period is seen at the start where there is little activity; this is followed by a gradually accelerating take-up of oxygen, giving an autocatalytic reaction ...

  5. Halcon process - Wikipedia

    en.wikipedia.org/wiki/Halcon_process

    The lighter analogue of propylene oxide, ethylene oxide, is produced by silver-catalyzed reaction of ethylene with oxygen. Attempts to implement this relatively simple technology to the conversion of propylene to propylene oxide fail. Instead only combustion predominates. The problems are attributed to the sensitivity of allylic C-H bonds.

  6. tert-Butyl hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_hydroperoxide

    tert-butyl hydroperoxide is potentially dangerous, but explosions are rare. [3]A solution of tert-butyl hydroperoxide and water with a concentration of greater than 90% is forbidden to be shipped according to US Department of Transportation Hazardous Materials Table 49 CFR 172.101.

  7. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohol can also be made by the rearrangement of propylene oxide, a reaction that is catalyzed by potassium alum at high temperature. The advantage of this method relative to the allyl chloride route is that it does not generate salt. Also avoiding chloride-containing intermediates is the "acetoxylation" of propylene to allyl acetate:

  8. Propylene chlorohydrin - Wikipedia

    en.wikipedia.org/wiki/Propylene_chlorohydrin

    Both are generated on a large scale as intermediates in the production of propylene oxide. [1] The reaction of aqueous solution of chlorine with propene gives a 10:1 ratio of CH 3 CH(OH)CH 2 Cl and CH 3 CH(Cl)CH 2 OH. These compounds are treated with lime to give propylene oxide, which is useful in the production of plastics and other polymers.

  9. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    ethylene oxide: basic chemicals, surfactants cyclohexane: K-A process: Co and Mn salts (homogeneous) cyclohexanol cyclohexanone: nylon precursor ethylene: Wacker process: Pd and Cu salts (homogeneous) acetaldehyde: basic chemicals para-xylene: terephthalic acid synthesis: Mn and Co salts (homogeneous) terephthalic acid: plastic precursor ...