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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.
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 ...
The main structure of chemical names according to IUPAC nomenclature. IUPAC nomenclature is a set of recommendations for naming chemical compounds and for describing chemistry and biochemistry in general. The International Union of Pure and Applied Chemistry (IUPAC) is the international authority on chemical nomenclature and terminology.
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 ...
Names of oxyanions should in general follow the names in Table X of the IUPAC 2005 Red Book. [2] Exceptions can be made if an alternate name is much more common in the literature, e.g. xenate rather than xenonate (don't generalise this to radon though, as it would create an ambiguity between radon and radium).
Basic IUPAC inorganic nomenclature has two main parts: the cation and the anion. The cation is the name for the positively charged ion and the anion is the name for the negatively charged ion. [14] An example of IUPAC nomenclature of inorganic chemistry is potassium chlorate (KClO 3): Potassium chlorate "Potassium" is the cation name.
Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.
[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 ...