enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Sodium percarbonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_percarbonate

    Sodium percarbonate or sodium carbonate peroxide is a chemical substance with empirical formula Na 2 H 3 CO 6. It is an adduct of sodium carbonate ("soda ash" or "washing soda") and hydrogen peroxide (that is, a perhydrate ) whose formula is more properly written as 2 Na 2 CO 3 · 3 H 2 O 2 .

  3. Schenck ene reaction - Wikipedia

    en.wikipedia.org/wiki/Schenck_ene_reaction

    The singlet oxygen reagent can be produced via photochemical activation of triplet oxygen (regular oxygen) in the presence of photosensitizers like rose bengal. Chemical processes like the reaction between hydrogen peroxide and sodium hypochlorite are also viable.

  4. Polycarbonate - Wikipedia

    en.wikipedia.org/wiki/Polycarbonate

    The main polycarbonate material is produced by the reaction of bisphenol A (BPA) and phosgene COCl 2. The overall reaction can be written as follows: The first step of the synthesis involves treatment of bisphenol A with sodium hydroxide, which deprotonates the hydroxyl groups of the bisphenol A. [6] (HOC 6 H 4) 2 CMe 2 + 2 NaOH → Na 2 (OC 6 ...

  5. Photo-oxidation of polymers - Wikipedia

    en.wikipedia.org/wiki/Photo-oxidation_of_polymers

    Charge-transfer complexes of oxygen and polystyrene phenyl groups absorb light to form singlet oxygen, which acts as a radical initiator. [23] Carbonyl impurities in the polymer (c.f. acetophenone) also absorb light in the near ultraviolet range (300 to 400 nm), forming excited ketones able to abstract hydrogen atoms directly from the polymer. [24]

  6. Juliá–Colonna epoxidation - Wikipedia

    en.wikipedia.org/wiki/Juliá–Colonna_epoxidation

    The Juliá–Colonna epoxidation is an asymmetric poly-leucine catalyzed nucleophilic epoxidation of electron deficient olefins in a triphasic system.The reaction was reported by Sebastian Juliá at the Chemical Institute of Sarriá in 1980, [1] with further elaboration by both Juliá and Stefano Colonna (Istituto di Chimica Industriale dell'Università, Milan, Italy).

  7. Diallyl carbonate - Wikipedia

    en.wikipedia.org/wiki/Diallyl_carbonate

    The Tsuji-Trost reaction was first introduced in 1962. This method played an important role in the synthesis of diallyl carbonate. The first mention of its commercial production dates back to 1982, when Tokuyama Corporation synthesized it for the first time using the sodium carbonate method.

  8. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The Dakin oxidation can occur in mild acidic conditions as well, with a mechanism analogous to the base-catalyzed mechanism. In methanol, hydrogen peroxide, and catalytic sulfuric acid, the carbonyl oxygen is protonated (14), after which hydrogen peroxide adds as a nucleophile to the carbonyl carbon, forming a tetrahedral intermediate (15).

  9. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Anthrahydroquinone reacts spontaneously with oxygen to form anthraquinone and hydrogen peroxide, possibly through some organic peroxide intermediate. After extraktion of the hydrogen peroxide the anthraquinone is catalytically reduced to anthrahydroquinone and reused in the process. There are other hydroquinones reacting in a similar fashion.