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  2. Sodium bisulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_bisulfite

    SO 2 + NaOH → NaHSO 3 SO 2 + NaHCO 3NaHSO 3 + CO 2. Attempts to crystallize the product yield sodium metabisulfite (also called sodium disulfite), Na 2 S 2 O 5. [6] Upon dissolution of the metabisulfite in water, bisulfite is regenerated: Na 2 S 2 O 5 + H 2 O → 2 Na + + 2 HSO 3 −. Sodium bisulfite is formed during the Wellman-Lord ...

  3. Sodium sulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_sulfite

    With more SO 2, the solid dissolves to give the disulfite, which crystallizes upon cooling. [2] SO 2 + 2 NaOH → Na 2 SO 3 + H 2 O. Sodium sulfite is made industrially by treating sulfur dioxide with a solution of sodium carbonate. [3] The overall reaction is: SO 2 + Na 2 CO 3 → Na 2 SO 3 + CO 2

  4. Sodium bisulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_bisulfate

    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).

  5. Bisulfite - Wikipedia

    en.wikipedia.org/wiki/Bisulfite

    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). HSO − 3 is a weak acidic species with a pK a of 6.97. Its conjugate base is sulfite, SO 23: HSO − 3SO 23 + H +

  6. Metal sulfur dioxide complex - Wikipedia

    en.wikipedia.org/wiki/Metal_sulfur_dioxide_complex

    This bonding mode is more common for early metals, which are typically strongly pi-donating. η 1-SO 2, O-bonded. In such cases, SO 2 attaches to a metal via one of its two oxygen centres. Such complexes are prevalent for hard metal cations such as Na + and Al 3+. In these compounds the M-O interaction is usually weak. [2]

  7. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    The sulfonyl functional group (RS(O) 2 R') has become an important electron-withdrawing group for modern organic chemistry. α-Sulfonyl carbanions may be used as nucleophiles in alkylation reactions, Michael-type additions, and other processes. [3] After having served their synthetic purpose, sulfonyl groups are often removed.

  8. Sulfite - Wikipedia

    en.wikipedia.org/wiki/Sulfite

    Sulfites or sulphites are compounds that contain the sulfite ion (systematic name: sulfate(IV) ion), SO 23. The sulfite ion is the conjugate base of bisulfite. Although its acid (sulfurous acid) is elusive, [1] its salts are widely used. Sulfites are substances that naturally occur in some foods and the human body.

  9. Sodium metabisulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_metabisulfite

    Sodium metabisulfite can be prepared by treating a solution of sodium hydroxide with sulfur dioxide. [3] When conducted in warm water, Na 2 SO 3 initially precipitates as a yellow solid. With more SO 2, the solid dissolves to give the disulfite, which crystallises upon cooling. [4] SO 2 + 2 NaOH → Na 2 SO 3 + H 2 O SO 2 + Na 2 SO 3 → Na 2 S ...