enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Peroxydisulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Peroxydisulfuric_acid

    The acid is prepared by the reaction of chlorosulfuric acid with hydrogen peroxide: [3] 2 ClSO 3 H + H 2 O 2 → H 2 S 2 O 8 + 2 HCl. Another method is the electrolysis of moderately concentrated sulfuric acid (60-70%) with platinum electrodes at high current density and voltage: H 2 SO 4 + H 2 O → H 3 O + + HSO 4 − (dissociation of ...

  3. Disulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Disulfuric_acid

    Disulfuric acid (alternative spelling disulphuric acid) or pyrosulfuric acid (alternative spelling pyrosulphuric acid), also named oleum, is a sulfur oxoacid. [3] It is a major constituent of fuming sulfuric acid, oleum , and this is how most chemists encounter it.

  4. Monsanto process - Wikipedia

    en.wikipedia.org/wiki/Monsanto_process

    The Monsanto process is an industrial method for the manufacture of acetic acid by catalytic carbonylation of methanol. [1] The Monsanto process has largely been supplanted by the Cativa process, a similar iridium-based process developed by BP Chemicals Ltd, which is more economical and environmentally friendly.

  5. Glossary of winemaking terms - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_winemaking_terms

    An acid that can be added to wine in order to halt yeast activity and alcohol production – such as in the production of some sweet wines. If a wine goes through malolactic fermentation when there is a significant amount of sorbic acid present, the wine can develop a fault characterized by a strong odor of crushed geraniums .

  6. Guerbet reaction - Wikipedia

    en.wikipedia.org/wiki/Guerbet_reaction

    These intermediates then react in an aldol condensation to the allyl aldehyde which the hydrogenation catalyst then reduces to the alcohol. [5] Guerbet Reaction Mechanism. The Cannizzaro reaction is a competing reaction when two aldehyde molecules react by disproportionation to form the corresponding alcohol and carboxylic acid.

  7. Mitsunobu reaction - Wikipedia

    en.wikipedia.org/wiki/Mitsunobu_reaction

    The reaction mechanism of the Mitsunobu reaction is fairly complex. The identity of intermediates and the roles they play has been the subject of debate. Initially, the triphenyl phosphine (2) makes a nucleophilic attack upon diethyl azodicarboxylate (1) producing a betaine intermediate 3, which deprotonates the carboxylic acid (4) to form the ion pair 5.

  8. Peroxy acid - Wikipedia

    en.wikipedia.org/wiki/Peroxy_acid

    Peroxymonosulfuric acid (Caro's acid) is probably the most important inorganic peracid, at least in terms of its production scale. [1] It is used for the bleaching of pulp and for the detoxification of cyanide in the mining industry. It is produced by treating sulfuric acid with hydrogen peroxide. Peroxymonophosphoric acid (H 3 PO 5) is ...

  9. Fischer–Speier esterification - Wikipedia

    en.wikipedia.org/wiki/Fischer–Speier...

    Acid chlorides evolve hydrogen chloride gas upon contact with atmospheric moisture, are corrosive, react vigorously with water and other nucleophiles (sometimes dangerously); they are easily quenched by other nucleophiles besides the desired alcohol; their most common synthesis routes involve the evolution of toxic carbon monoxide or sulfur ...