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Sodium bisulfite (or sodium bisulphite, sodium hydrogen sulfite) is a chemical mixture with the approximate chemical formula NaHSO 3. Sodium bisulfite is not a real compound, [ 2 ] but a mixture of salts that dissolve in water to give solutions composed of sodium and bisulfite ions.
In this reaction an aromatic hydroxyl group is converted to the corresponding amine group. This is a reversible reaction. The first step in this reaction is an addition reaction of sodium bisulfite to an aromatic double bond. The Bucherer carbazole synthesis is a related organic reaction that uses sodium bisulfite as a reagent.
Aside from using sodium thiosulfate as a substrate, cysteine can also be used. [2] Iodide from potassium iodide is converted to iodine in the first reaction: 2 I − + 2 H + + H 2 O 2 → I 2 + 2 H 2 O The iodine produced in the first reaction is reduced back to iodide by the reducing agent, cysteine. At the same time, cysteine is oxidized into ...
Sodium bisulfate is produced as an intermediate in the Mannheim process, an industrial process involving the reaction of sodium chloride and sulfuric acid: [1] NaCl + H 2 SO 4 → HCl + NaHSO 4. The process for the formation of sodium bisulfate is highly exothermic. The liquid sodium bisulfate is sprayed and cooled so that it forms a solid bead.
Similar reactions are effected with divalent cations (Mg2+, Ca2+) and using carbonates in place of hydroxide. The ratio of sulfite to bisulfite depends on pH; above pH=7, sulfite predominates. Calcium-based. The earliest process used calcium, obtained as inexpensive calcium carbonate, and there was little incentive to recover the inorganic ...
The Schiff reagent is the reaction product of a dye formulation such as fuchsin and sodium bisulfite; pararosaniline (which lacks an aromatic methyl group) and new fuchsin (which is uniformly mono-methylated ortho to the dye's amine functionalities) are not dye alternatives with comparable detection chemistry.
The Bucherer carbazole synthesis is a chemical reaction used to synthesize carbazoles from naphthols and aryl hydrazines using sodium bisulfite. The reaction is named after Hans Theodor Bucherer. The Bucherer carbazole synthesis
Sodium sulfite used industrial as a corrosion inhibitor/oxygen scavenger. Monoprotonation of sulfite gives HSO 3 −, which is called bisulfite. The sodium and potassium salts of bisulfite are not available, but solid and solutions of the approximate formula NaHSO 3 and KHSO 3 are widely marketed as sodium bisulfite and potassium bisulfite.