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  2. Arsenic tribromide - Wikipedia

    en.wikipedia.org/wiki/Arsenic_tribromide

    2 As 2 O 3 + 3 S + 6 Br 2 → 4 AsBr 3 + 3 SO 2. Arsenic tribromide is a highly water soluble crystalline arsenic source for uses compatible with bromides and lower (acidic) pH. Most metal bromide compounds are water soluble for uses in water treatment, chemical analysis and in ultra high purity for certain crystal growth applications.

  3. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC states that, "As one of its major activities, IUPAC develops Recommendations to establish unambiguous, uniform, and consistent nomenclature and terminology for specific scientific fields, usually presented as: glossaries of terms for specific chemical disciplines; definitions of terms relating to a group of properties; nomenclature of chemical compounds and their classes; terminology ...

  4. Aluminium bromide - Wikipedia

    en.wikipedia.org/wiki/Aluminium_bromide

    A demonstration of the reaction of the exothermic reaction of the strong Lewis acid (Al 2 Br 6) and strong Lewis base (H 2 O). Al 2 Br 6 dissociates readily to give the strong Lewis acid , AlBr 3 . Regarding the tendency of Al 2 Br 6 to dimerize , it is common for heavier main group halides to exist as aggregates larger than implied by their ...

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    3 COOH, which is commonly called acetic acid and is also its recommended IUPAC name, but its formal, systematic IUPAC name is ethanoic acid. The IUPAC's rules for naming organic and inorganic compounds are contained in two publications, known as the Blue Book [1] [2] and the Red Book, [3] respectively.

  6. Phosphorus tribromide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_tribromide

    [5] [6] In some cases, triphenylphosphine/Br 2 is superior to PBr 3. [7] The mechanism for a primary alcohol involves formation of a phosphorous ester (to form a good leaving group), followed by an S N 2 substitution. Because of the S N 2 substitution step, the reaction generally works well for primary and secondary alcohols, but fails for ...

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, (CH 3) 2 CHCH 3, commonly known as isobutane, is treated as a propane chain with a methyl group bonded to the middle (2) carbon, and given the systematic name 2-methylpropane. However, although the name 2-methylpropane could be used, it is easier and more logical to call it simply methylpropane – the methyl group could not ...

  8. Acetyl bromide - Wikipedia

    en.wikipedia.org/wiki/Acetyl_bromide

    As is expected, it may be prepared by reaction between phosphorus tribromide and acetic acid: [2] 3 CH 3 COOH + PBr 3 → 3 CH 3 COBr + H 3 PO 3. As usual for an acid halide, acetyl bromide hydrolyzes rapidly in water, forming acetic acid and hydrobromic acid. It also reacts with alcohols and amines to produce acetate esters and acetamides ...

  9. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    It is somewhat soluble in water and readily evaporates into the air. Bromoform is the main trihalomethane produced in beachfront salt water swimming pools with concentrations as high as 1.2 ppm (parts per million). Concentrations in freshwater pools are 1000 times lower. [9] Occupational skin exposure limits are set at 0.5 ppm. [10]