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  2. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  3. Sodium bisulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_bisulfite

    SO 2 + NaOH → NaHSO 3 SO 2 + NaHCO 3 → NaHSO 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 ...

  4. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure.

  5. Sodium sulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_sulfite

    When conducted in warm water, Na 2 SO 3 initially precipitates as a white solid. 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:

  6. Sodium metabisulfite - Wikipedia

    en.wikipedia.org/wiki/Sodium_metabisulfite

    Sodium metabisulfite or sodium pyrosulfite (IUPAC spelling; Br. E. sodium metabisulphite or sodium pyrosulphite) is an inorganic compound of chemical formula Na 2 S 2 O 5. The substance is sometimes referred to as disodium metabisulfite. It is used as a disinfectant, antioxidant, and preservative agent. [2] When dissolved in water it forms ...

  7. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    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.

  8. Sodium hydrosulfide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydrosulfide

    NaSH and sodium sulfide are used industrially, often for similar purposes. Solid NaSH is colorless. The solid has an odor of H 2 S owing to hydrolysis by atmospheric moisture. In contrast with sodium sulfide (Na 2 S), which is insoluble in organic solvents, NaSH, being a 1:1 electrolyte, is more soluble.

  9. 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).

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