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  2. Bromine - Wikipedia

    en.wikipedia.org/wiki/Bromine

    Bromine was discovered independently by two chemists, Carl Jacob Löwig [13] and Antoine Balard, [14] [15] in 1825 and 1826, respectively. [16] Löwig isolated bromine from a mineral water spring from his hometown Bad Kreuznach in 1825. Löwig used a solution of the mineral salt saturated with chlorine and extracted the bromine with diethyl ...

  3. Color of chemicals - Wikipedia

    en.wikipedia.org/wiki/Color_of_chemicals

    The color of chemicals is a physical property of chemicals that in most cases comes from the excitation of electrons due to an absorption of energy performed by the chemical. The study of chemical structure by means of energy absorption and release is generally referred to as spectroscopy .

  4. 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)).

  5. CPK coloring - Wikipedia

    en.wikipedia.org/wiki/CPK_coloring

    Several of the CPK colors refer mnemonically to colors of the pure elements or notable compound. For example, hydrogen is a colorless gas, carbon as charcoal, graphite or coke is black, sulfur powder is yellow, chlorine is a greenish gas, bromine is a dark red liquid, iodine in ether is violet, amorphous phosphorus is red, rust is dark orange-red, etc.

  6. Bromothymol blue - Wikipedia

    en.wikipedia.org/wiki/Bromothymol_blue

    Bromothymol blue acts as a weak acid in a solution. It can thus be in protonated or deprotonated form, appearing yellow or blue, respectively. It is bright aquamarine by itself, and greenish-blue in a neutral solution. The deprotonation of the neutral form results in a highly conjugated structure, accounting for the difference in color. An ...

  7. 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 ...

  8. Bromide - Wikipedia

    en.wikipedia.org/wiki/Bromide

    Bromine readily reacts with water, i.e. it undergoes hydrolysis: Br 2 + H 2 O → HOBr + HBr. This forms hypobromous acid (HOBr), and hydrobromic acid (HBr in water). The solution is called "bromine water". The hydrolysis of bromine is more favorable in the presence of base, for example sodium hydroxide: Br 2 + NaOH → NaOBr + NaBr

  9. Potassium bromide - Wikipedia

    en.wikipedia.org/wiki/Potassium_bromide

    A bottle of PRN Pharmaceutical Company (Pensacola, FL) K•BroVet veterinary pharmaceutical potassium bromide oral solution (250 mg/mL). The product is intended to be used in dogs, primarily as an antiepileptic (to stop seizures). [5] The pink color of the solution is artificial; pure potassium bromide solutions are colorless