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[3] [4] Antichlors are very useful in the textile industry because bleaching of compounds using chlorine is a standard practice. However, the use of sodium bisulfite in the decomposition of excess hypochlorite can lead to harmful byproducts when it comes into contact with water at the concentrations present for industrial use. [4]
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).
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).
Of academic interest, SO 2 acts like a Lewis acid towards the alkyl ligand. [4] The pathway for the insertion of SO 2 into metal alkyl bond begins with attack of the alkyl nucleophile on the sulfur centre in SO 2. The "insertion" proceed the sulfur dioxide between the metal and the alkyl ligand leads to the O, O'-sulphinate.
This also called '3:2 mullite' to distinguish it from 2Al 2 O 3 ·SiO 2, Al 4 SiO 8 '2:1 mullite'. 2Al 2 O 3 ·SiO 2, Al 4 SiO 8 '2:1 mullite'. [6] The above list mentions ternary materials (Si-Al-O). Kaolinite is a quaternary material (Si-Al-O-H). Also called aluminium silicate dihydrate, kaolinite occurs naturally as a mineral. Its formula is ...
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.
[4] The structure of the sulfite anion can be described with three equivalent resonance structures . In each resonance structure, the sulfur atom is double-bonded to one oxygen atom with a formal charge of zero (neutral), and sulfur is singly bonded to the other two oxygen atoms, which each carry a formal charge of −1, together accounting for ...
Aluminum amalgam (Al/Hg) may be used for the chemoselective reduction of α-sulfonylated carbonyl groups. Carboxylic acid derivatives, acetals, thioacetals, amines, alcohols, and isolated double bonds are all inert to Al/Hg. Selective desulfonylation may be carried out on β-hydroxy sulfones without reductive elimination.