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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.
The bisulfite ion (IUPAC-recommended nomenclature: hydrogensulfite) is the ion HSO − 3. Salts containing the HSO − 3 ion are also known as "sulfite lyes". [1] Sodium bisulfite is used interchangeably with sodium metabisulfite (Na 2 S 2 O 5). Sodium metabisulfite dissolves in water to give a solution of Na + HSO − 3. Na 2 S 2 O 5 + H 2 O ...
Sodium bisulfate, also known as sodium hydrogen sulfate, [a] is the sodium salt of the bisulfate anion, with the molecular formula NaHSO 4. Sodium bisulfate is an acid salt formed by partial neutralization of sulfuric acid by an equivalent of sodium base, typically in the form of either sodium hydroxide (lye) or sodium chloride (table salt).
Sodium sulfite (sodium sulphite) is the inorganic compound with the chemical formula Na 2 SO 3. A white, water-soluble solid, it is used commercially as an antioxidant and preservative. It is also suitable for the softening of lignin in the pulping and refining processes of wood and lignocellulosic materials. [1]
Upon formation of the adduct, a new extended phase is formed in which the gas molecules are incorporated (inserted) as ligands of the copper atoms within the structure. This reaction can also be considered a reaction between a base and a Lewis acid where the copper atom plays the electron-receiving role and the pi electrons of the gas molecule ...
The enamine eliminates sodium bisulfite with formation of naphthylamine 6. It is important to stress that this is a reversible reaction. The reaction is summarized as follows: The Bucherer carbazole synthesis is a related reaction.
Hydroxysultaine is prepared industrially by the reaction of sodium bisulfite with epichlorohydrin to give the sodium salt (sodium 1-chloro-2-hydroxypropane sulfonate). [1] This is similar to the synthesis of isethionate , which is also used as a 'head-group' in surfactants.
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 ...