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Sulfuric acid (American spelling and the preferred IUPAC name) or sulphuric acid (Commonwealth spelling), known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, and hydrogen, with the molecular formula H 2 SO 4. It is a colorless, odorless, and viscous liquid that is miscible with water. [7] Structure ...
Aqua fortis /spirit of nitre – nitric acid, formed by 2 parts saltpetre in 1 part (pure) oil of vitriol (sulfuric acid). (Historically, this process could not have been used, as 98% oil of vitriol was not available.) Aqua ragia /spirit of turpentine/oil of turpentine/gum turpentine – turpentine, formed by the distillation of pine tree resin.
For sulfuric acid, computational analysis (with natural bond orbitals) confirms a clear positive charge on sulfur (theoretically +2.45) and a low 3d occupancy. Therefore, the representation with four single bonds is the optimal Lewis structure rather than the one with two double bonds (thus the Lewis model, not the Pauling model).
Oleum is produced in the contact process, where sulfur is oxidized to sulfur trioxide which is subsequently dissolved in concentrated sulfuric acid. [3] Sulfuric acid itself is regenerated by dilution of part of the oleum. The lead chamber process for sulfuric acid production was abandoned, partly because it could not produce sulfur trioxide or ...
This is an accepted version of this page This is the latest accepted revision, reviewed on 21 February 2025. This article is about the chemical element. For other uses, see Sulfur (disambiguation). Chemical element with atomic number 16 (S) Sulfur, 16 S Sulfur Alternative name Sulphur (pre-1992 British spelling) Allotropes see Allotropes of sulfur Appearance Lemon yellow sintered microcrystals ...
(of a chemical species) Tending to behave both as an acid and as a base, depending upon the medium in which the species is situated; e.g. sulfuric acid (H 2 SO 4) is a strong acid in water but behaves more like a base in superacids. amyl A common non-systematic name for a pentyl group. analyte
In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure R−O−SO − 3. The SO 4 core is a sulfate group and the R group is any organic residue. All organosulfates are formally esters derived from alcohols and sulfuric acid (H 2 SO 4) although many
An acid which has more of a tendency to donate a hydrogen ion than the limiting acid will be a strong acid in the solvent considered, and will exist mostly or entirely in its dissociated form. Likewise, the limiting base in a given solvent is the solvate ion, such as OH − ( hydroxide ) ion, in water.