When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Pyrogallol - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol

    Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .

  3. Pyrogallol 1,2-oxygenase - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol_1,2-oxygenase

    This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O 2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O 2. The systematic name of this enzyme class is 1,2,3-trihydroxybenzene:oxygen 1,2-oxidoreductase ...

  4. Pyrogallol hydroxytransferase - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol_hydroxytransferase

    In enzymology, a pyrogallol hydroxytransferase (EC 1.97.1.2) is an enzyme that catalyzes the chemical reaction 1,2,3,5-tetrahydroxybenzene + 1,2,3-trihydroxybenzene ⇌ {\displaystyle \rightleftharpoons } 1,3,5-trihydroxybenzene + 1,2,3,5-tetrahydroxybenzene

  5. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    Of the two half reactions, the oxidation step is the most demanding because it requires the coupling of 4 electron and proton transfers and the formation of an oxygen-oxygen bond. This process occurs naturally in plants photosystem II to provide protons and electrons for the photosynthesis process and release oxygen to the atmosphere, [ 1 ] as ...

  6. Hydrogenolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrogenolysis

    Hydrogenolysis is a chemical reaction whereby a carbon–carbon or carbon–heteroatom single bond is cleaved or undergoes lysis (breakdown) by hydrogen. [1] The heteroatom may vary, but it usually is oxygen, nitrogen, or sulfur. A related reaction is hydrogenation, where hydrogen is added to the molecule, without cleaving bonds. Usually ...

  7. Hydroxylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxylation

    In biochemistry, hydroxylation reactions are often facilitated by enzymes called hydroxylases. These enzymes insert an O atom into a C−H bond. Typical stoichiometries for the hydroxylation of a generic hydrocarbon are these: 2R 3 C−H + O 2 → 2 R 3 C−OH R 3 C−H + O 2 + 2e − + 2H + → R 3 C−OH + H 2 O

  8. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula −OH and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry , alcohols and carboxylic acids contain one or more hydroxy groups.

  9. Woodward–Hoffmann rules - Wikipedia

    en.wikipedia.org/wiki/Woodward–Hoffmann_rules

    Thermolysis converts 1 to (E,E) geometric isomer 2, but 3 to (E,Z) isomer 4.. The Woodward–Hoffmann rules (or the pericyclic selection rules) [1] are a set of rules devised by Robert Burns Woodward and Roald Hoffmann to rationalize or predict certain aspects of the stereochemistry and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.