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Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .
Syringol is the organic compound with the formula HO(CH 3 O) 2 C 6 H 3. The molecule is a phenol, with methoxy groups in the flanking (2 and 6) positions. It is the symmetrically dimethylated derivative of pyrogallol. It is a colorless solid, although typical samples are brown owing to air-oxidized impurities.
Phloroglucinol is an organic compound with the formula C 6 H 3 (OH) 3. It is a colorless solid. It is used in the synthesis of pharmaceuticals and explosives. Phloroglucinol is one of three isomeric benzenetriols. The other two isomers are hydroxyquinol (1,2,4-benzenetriol) and pyrogallol (1,2,3-benzenetriol).
By reacting the bromopyrogallol red with niobium(V) in a tartrate medium at pH 6.0, an intense blue coloured 3:1 reagent was formed. The sensitivity and conditional selectivity of bromopyrogallol red was also studied and results show that trace amounts of silver can be detected from the formation of a ternary complex between 1,10-phenanthroline, bromopyrogallol red and silver ion.
Oxygen can form oxides with heavier noble gases xenon and radon, although this needs indirect methods. Even though no oxides of krypton are known, oxygen is able to form covalent bonds with krypton in an unstable compound Kr(OTeF 5) 2. One unexpected oxygen compound is dioxygenyl hexafluoroplatinate, O + 2 PtF −
Sulfuric acid contains two hydroxy groups.. Water, alcohols, carboxylic acids, and many other hydroxy-containing compounds can be readily deprotonated due to a large difference between the electronegativity of oxygen (3.5) and that of hydrogen (2.1).
The Dakin oxidation can occur in mild acidic conditions as well, with a mechanism analogous to the base-catalyzed mechanism. In methanol, hydrogen peroxide, and catalytic sulfuric acid, the carbonyl oxygen is protonated (14), after which hydrogen peroxide adds as a nucleophile to the carbonyl carbon, forming a tetrahedral intermediate (15).
The free radicals generated by this process engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. [6] Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.