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  2. Vanadium bromoperoxidase - Wikipedia

    en.wikipedia.org/wiki/Vanadium_bromoperoxidase

    Vanadium bromoperoxidases have been found in bacteria, fungi, marine macro algae (), and marine microalgae which produce brominated organic compounds. [2]It has not been definitively identified as the bromoperoxidase of higher eukaryotes, such as murex snails, which have a very stable and specific bromoperoxidase, but perhaps not a vanadium dependent one. [3]

  3. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    The enzyme vanadium bromoperoxidase, one of a larger family of bromoperoxidases, catalyzes this reaction in the marine environment. [9] The oceans are estimated to release 1–2 million tons of bromoform and 56,000 tons of bromomethane annually. [ 10 ]

  4. Committed step - Wikipedia

    en.wikipedia.org/wiki/Committed_step

    In biochemistry, the committed step (also known as the first committed step) is an effectively irreversible, enzyme-catalyzed reaction that occurs at a branch point during the biosynthesis of some molecules. [1] [2] As the name implies, after this step, the molecules are "committed" to the pathway and will ultimately end up in the pathway's ...

  5. Bromide peroxidase - Wikipedia

    en.wikipedia.org/wiki/Bromide_peroxidase

    Bromide peroxidase (EC 1.11.1.18, bromoperoxidase, haloperoxidase (ambiguous), eosinophil peroxidase) is a family of enzymes with systematic name bromide:hydrogen-peroxide oxidoreductase. These enzymes catalyse the following chemical reaction: [1] [2] [3] HBr + H 2 O 2 HOBr + H 2 O. The HOBr is a potent brominating agent.

  6. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Likewise, 1-chloropropane and 2-chloropropane give propene. Zaitsev's rule helps to predict regioselectivity for this reaction type. In general, the reaction of a haloalkane with potassium hydroxide can compete with an S N 2 nucleophilic substitution reaction by OH − a strong, unhindered nucleophile. Alcohols are however generally minor products.

  7. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert -butyl group attached to a bromide substituent.

  8. Bromotoluene - Wikipedia

    en.wikipedia.org/wiki/Bromotoluene

    184.5 °c (364.1 °f; 457.7 k) Benzyl bromide is an isomer, which has a bromine substituted for one of the hydrogens of toluene 's methyl group, and it is sometimes named α-bromotoluene. Preparation

  9. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    Occupational exposure to 1-bromopropane typically occurs through breathing or skin contact; it is easily absorbed into the blood via the skin. Replacing 1-bromopropane with water or acetone-based adhesives is the preferred NIOSH option for controlling occupational exposure, but other options include engineering controls like isolation and ...