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  2. Bromine test - Wikipedia

    en.wikipedia.org/wiki/Bromine_test

    In organic chemistry, the bromine test is a qualitative test for the presence of unsaturation (carbon-to-carbon double or triple bonds), phenols and anilines. An unknown sample is treated with a small amount of elemental bromine in an organic solvent, being as dichloromethane or carbon tetrachloride. Presence of unsaturation and/or phenol or ...

  3. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Another method is halogen exchange in the presence of excess "halogenating reagent", for example: [41] FeCl 3 + BBr 3 (excess) → FeBr 3 + BCl 3. When a lower bromide is wanted, either a higher halide may be reduced using hydrogen or a metal as a reducing agent, or thermal decomposition or disproportionation may be used, as follows: [41]

  4. Photochlorination - Wikipedia

    en.wikipedia.org/wiki/Photochlorination

    In the presence of oxygen, the hydrogen bromide formed is partly oxidised back to bromine, resulting in an increased yield. Because of the easier dosage of the elemental bromine and the higher selectivity of the reaction, photobromination is preferred over photochlorination at laboratory scale.

  5. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    In oxychlorination, the combination of hydrogen chloride and oxygen serves as the equivalent of chlorine, as illustrated by this route to 1,2-dichloroethane: 4 HCl + 2 CH 2 =CH 2 + O 2 → 2 Cl−CH 2 −CH 2 −Cl + 2 H 2 O Structure of a bromonium ion. The addition of halogens to alkenes proceeds via intermediate halonium ions. In special ...

  6. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    The relative rates at which different halogens react vary considerably: [citation needed] fluorine (108) > chlorine (1) > bromine (7 × 10 −11) > iodine (2 × 10 −22).. Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction.

  7. Rancidification - Wikipedia

    en.wikipedia.org/wiki/Rancidification

    The double bonds of an unsaturated fatty acid can be cleaved by free-radical reactions involving molecular oxygen. This reaction causes the release of malodorous and highly volatile aldehydes and ketones. Because of the nature of free-radical reactions, the reaction is catalyzed by sunlight. [7] Oxidation primarily occurs with unsaturated fats.

  8. Light-dependent reactions - Wikipedia

    en.wikipedia.org/wiki/Light-dependent_reactions

    Then in 1939, Robin Hill demonstrated that isolated chloroplasts would make oxygen, but not fix CO 2, showing the light and dark reactions occurred in different places. Although they are referred to as light and dark reactions, both of them take place only in the presence of light. [12] This led later to the discovery of photosystems I and II.

  9. Bromine water - Wikipedia

    en.wikipedia.org/wiki/Bromine_water

    Bromine water, Br 2. Bromine water is an oxidizing, intense brown mixture containing diatomic bromine (Br 2) dissolved in water (H 2 O). [1] It is often used as a reactive in chemical assays of recognition for substances which react with bromine in an aqueous environment with the halogenation mechanism, mainly unsaturated carbon compounds (carbon compounds with 1 or more double or triple bond(s)).