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  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 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 ...

  4. 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 ...

  5. Binding site - Wikipedia

    en.wikipedia.org/wiki/Binding_site

    However, when the reaction takes place while the enzyme is bound to a substrate, the kinetics play out differently. [34] Modeling with binding curves are useful when evaluating the binding affinities of oxygen to hemoglobin and myoglobin in the blood. Hemoglobin, which has four heme groups, exhibits cooperative binding. This means that the ...

  6. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The two hydrogen 1s orbitals are premixed to form a 1 (σ) and b 2 (σ*) MO. Mixing takes place between same-symmetry orbitals of comparable energy resulting a new set of MO's for water: 2a 1 MO from mixing of the oxygen 2s AO and the hydrogen σ MO. 1b 2 MO from mixing of the oxygen 2p y AO and the hydrogen σ* MO. 3a 1 MO from mixing of the a ...

  7. 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 ...

  8. 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

  9. 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.