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Alternatively, sulfides can be synthesized by the addition of a thiol to an alkene in the thiol-ene reaction: R-CH=CH 2 + H-SR' → R-CH 2-CH 2-S-R' This reaction is often catalysed by free radicals produced from a photoinitiator. [6] Sulfides can also be prepared by many other methods, such as the Pummerer rearrangement. Trialkysulfonium salts ...
In organic chemistry, a thiol (/ ˈ θ aɪ ɒ l /; [1] from Ancient Greek θεῖον (theion) 'sulfur' [2]), or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a ...
Humans and other animals have an exquisitely sensitive sense of smell toward the odor of low-valent organosulfur compounds such as thiols, sulfides, and disulfides. Malodorous volatile thiols are protein-degradation products found in putrid food, so sensitive identification of these compounds is crucial to avoiding intoxication.
Some metal sulfides, when exposed to a strong mineral acid, including gastric acids, will release toxic hydrogen sulfide. Organic sulfides are highly flammable. When a sulfide burns it produces sulfur dioxide (SO 2) gas. Hydrogen sulfide, some of its salts, and almost all organic sulfides have a strong and putrid stench; rotting biomass ...
Download QR code; Print/export Download as PDF; Printable version; ... Pages in category "Sulfides" The following 81 pages are in this category, out of 81 total.
Of these the thiol form is most common (e.g. thioacetic acid). Thiocarboxylic acids are rare in nature, however the biosynthetic components for producing them appear widespread in bacteria . [ 3 ] Examples include pyridine-2,6-dicarbothioic acid , [ 4 ] and thioquinolobactin.
Thiophenol is an organosulfur compound with the formula C 6 H 5 SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic thiol.The chemical structures of thiophenol and its derivatives are analogous to phenols, where the oxygen atom in the hydroxyl group (-OH) bonded to the aromatic ring in phenol is replaced by a sulfur atom.
Download QR code; Print/export Download as PDF; Printable version; ... Pages in category "Thiols" The following 91 pages are in this category, out of 91 total.