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  2. Ninhydrin - Wikipedia

    en.wikipedia.org/wiki/Ninhydrin

    Ninhydrin (2,2-dihydroxyindane-1,3-dione) is an organic compound with the formula C 6 H 4 (CO) 2 C(OH) 2.It is used to detect ammonia and amines.Upon reaction with these amines, ninhydrin gets converted into deep blue or purple derivatives, which are called Ruhemann's purple.

  3. NOx - Wikipedia

    en.wikipedia.org/wiki/NOx

    The symbol represents a "third body", a molecular species that is required to carry away energy from the exothermic reaction 2.Equation 4 relates the concentrations of NO x and ozone, and is known as the Leighton relationship.

  4. Aniline - Wikipedia

    en.wikipedia.org/wiki/Aniline

    Aniline (from Portuguese anil 'indigo shrub', and -ine indicating a derived substance) [6] is an organic compound with the formula C 6 H 5 NH 2.Consisting of a phenyl group (−C 6 H 5) attached to an amino group (−NH 2), aniline is the simplest aromatic amine.

  5. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    "Redox" is a portmanteau of the words "REDuction" and "OXidation." The term "redox" was first used in 1928. [6]Oxidation is a process in which a substance loses electrons. Reduction is a process in which a substance gains electr

  6. Oxidoreductase - Wikipedia

    en.wikipedia.org/wiki/Oxidoreductase

    In biochemistry, an oxidoreductase is an enzyme that catalyzes the transfer of electrons from one molecule, the reductant, also called the electron donor, to another, the oxidant, also called the electron acceptor.

  7. Nitrate reductase - Wikipedia

    en.wikipedia.org/wiki/Nitrate_reductase

    Prokaryotic nitrate reductases belong to the DMSO reductase family of molybdoenzymes and have been classified into three groups, assimilatory nitrate reductases (Nas), respiratory nitrate reductase (Nar), and periplasmic nitrate reductases (Nap). [3]

  8. Bouveault–Blanc reduction - Wikipedia

    en.wikipedia.org/wiki/Bouveault–Blanc_reduction

    The Bouveault–Blanc reduction is a chemical reaction in which an ester is reduced to primary alcohols using absolute ethanol and sodium metal. [1] It was first reported by Louis Bouveault and Gustave Louis Blanc in 1903.

  9. Ketone halogenation - Wikipedia

    en.wikipedia.org/wiki/Ketone_halogenation

    Halogenation of α,β-unsaturated ketone [3]. On α,β-Unsaturated ketones or enones, it's possible to halogenate with iodine selectively on the more saturated alpha on the ketone selectively over the unsaturated side.