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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.
4 KO 2 + 4 CO 2 + 2 H 2 O → 4 KHCO 3 + 3 O 2. Theoretically, 1 kg of KO 2 absorbs 0.310 kg of CO 2 while releasing 0.338 kg of O 2. One mole of KO 2 absorbs 0.5 moles of CO 2 and releases 0.75 moles of oxygen. Potassium superoxide finds only niche uses as a laboratory reagent. Because it reacts with water, KO 2 is often studied in
Desulfonylation reactions are chemical reactions leading to the removal of a sulfonyl group from organic compounds.As the sulfonyl functional group is electron-withdrawing, [1] methods for cleaving the sulfur–carbon bonds of sulfones are typically reductive in nature.
Solutions of bisulfite are typically prepared by treatment of sulfur dioxide with aqueous base: [3]. SO 2 + OH − → HSO − 3. HSO − 3 is the conjugate base of sulfurous acid, (H 2 SO 3).
Although nearly 100% sulfuric acid solutions can be made, the subsequent loss of SO 3 at the boiling point brings the concentration to 98.3% acid. The 98.3% grade, which is more stable in storage, is the usual form of what is described as "concentrated sulfuric acid".
Sulfoxylic acid (H 2 SO 2) (also known as hyposulfurous acid or sulfur dihydroxide [1]) is an unstable oxoacid of sulfur in an intermediate oxidation state between hydrogen sulfide and dithionous acid.
Molecular models of the different molecules active in Piranha solution: peroxysulfuric acid (H 2 SO 5) and hydrogen peroxide (H 2 O 2). Piranha solution, also known as piranha etch, is a mixture of sulfuric acid (H 2 SO 4) and hydrogen peroxide (H 2 O 2).
Sulfurous acid is commonly known to not exist in its free state, and due to this, it is stated in textbooks that it cannot be isolated in the water-free form. [4] However, the molecule has been detected in the gas phase in 1988 by the dissociative ionization of diethyl sulfite. [5]