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Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.
Bromotoluenes are aryl bromides based on toluene in which at least one aromatic hydrogen atom is replaced with a bromine atom. They have the general formula C 7 H 8– n Br n , where n = 1–5 is the number of bromine atoms.
bromine chloride: 13863-41-7 BrCl 3: bromine trichloride: 12360-50-8 BrCl 5: bromine pentachloride: BrF: bromine monofluoride bromine fluoride: 13863-59-7 BrF 3: bromine trifluoride: 7787-71-5 BrF 5: bromine pentafluoride: 7789-30-2 BrI iodine monobromide: 7789-33-5 BrO 3 −: bromate ion: 15541-45-4 Br 2: bromine: 7726-95-6 Br 2 O 5: dibromine ...
List of boiling and freezing information of solvents. ... Download as PDF; Printable version; In other projects ... Toluene: 0.82 110.6 [28] Dimethyl Sulfoxide: 189.0
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Toluene (or methylbenzene) is a common chemical found in chemistry laboratories. An alkylbenzene is a chemical compound that contains a monocyclic aromatic ring attaching to one or more saturated hydrocarbon chains. [1] Alkylbenzenes are derivatives of benzene, in which one or more hydrogen atoms are replaced by alkyl groups.
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In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1] [2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]