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Iron(III) chloride has been shown to promote C-C coupling reaction. [48] Several reagents have been developed based on supported iron(III) chloride. On silica gel, the anhydrous salt has been applied to certain dehydration and pinacol-type rearrangement reactions. A similar reagent but moistened induces hydrolysis or epimerization reactions. [49]
The sodium fusion extract is made alkaline by adding NaOH. To this mixture, freshly prepared FeSO 4 solution is added and boiled for some time and then cooled. A few drops of FeCl 3 are added and Prussian blue (bluish green) color forms due to formation of ferric ferrocyanide along with NaCl. This shows the presence of nitrogen in the organic ...
Add sodium hydroxide to the mixture until a permanent brown precipitate is formed. The formation of a red, blue, green, or purple coloration indicates the presence of phenols. Where the sample is insoluble in water, it may be dissolved in dichloromethane with a small amount of pyridine .
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.
This reaction can be used to remove potassium hexacyanidoferrate(II) from a solution. [citation needed] A famous reaction involves treatment with ferric salts, most commonly Iron(III) chloride, to give Prussian blue. In the reaction with Iron(III) chloride, producing Potassium chloride as a side-product:
NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates and can be collected by filtration. [1] Crude NBS gives better yield in the Wohl–Ziegler reaction. In other cases, impure NBS (slightly yellow in ...
The reaction proceeds through generation of an acylium center. The reaction is completed by deprotonation of the arenium ion by AlCl 4 −, regenerating the AlCl 3 catalyst. However, in contrast to the truly catalytic alkylation reaction, the formed ketone is a moderate Lewis base, which forms a complex with the strong Lewis acid aluminum ...
Fe(acac) 3 has been examined as a precatalyst and reagent in organic chemistry, although the active iron-containing species is usually unidentified in these processes. In one instance, Fe(acac) 3 was shown to promote cross-coupling a diene to an olefin. [5]