Dithionic acid

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Dithionic acid
Dithionic-acid-2D.png
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Names
IUPAC name
dithionic acid [1]
Other names
hypodisulfuric acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
PubChem CID
UNII
  • InChI=1S/H2O6S2/c1-7(2,3)8(4,5)6/h(H,1,2,3)(H,4,5,6) Yes check.svgY
    Key: RMGVZKRVHHSUIM-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/H2O6S2/c1-7(2,3)8(4,5)6/h(H,1,2,3)(H,4,5,6)
    Key: RMGVZKRVHHSUIM-UHFFFAOYAM
  • O=S(=O)(O)S(=O)(=O)O
Properties
H2S2O6
Molar mass 162.14 g mol−1
Acidity (pKa)-3.4 (estimated) [2]
Conjugate base Dithionate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dithionic acid, H2S2O6, is a chemical compound known only in solution. [3]

Contents

Salts

Dithionic acid is diprotic and salts called dithionates are known. No acid salts (i.e.: one proton lost) have been discovered. All dithionates are readily soluble in water. [3] They are mild oxidizing and mild reducing agents. The shape of the dithionate ion is like ethane, but two SO3 groups adopt an almost eclipsed conformation. The S—S bond length is about 2.15 Å; the S—O bonds are rather short with a bond length of 1.43 Å.

Synthesis

Dithionates can be made by oxidizing a sulfite (from the +4 to the +5 oxidation state), but on a larger scale they are made by oxidizing a cooled aqueous solution of sulfur dioxide with manganese dioxide:

2 MnO2 + 3 SO2 → MnS2O6 + MnSO4

The manganese dithionate solution formed can then be converted to dithionate salts of other metals by metathesis reactions:

Ba2+(aq) + MnS2O6(aq) + MnSO4(aq) → BaSO4(s)↓ + BaS2O6·2H2O(aq)

Concentrated solutions of dithionic acid can subsequently be obtained treating a barium dithionate solution with sulfuric acid:

BaS2O6(aq) + H2SO4(aq) → H2S2O6(aq) + BaSO4(s)↓

See also

Related Research Articles

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4
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<span class="mw-page-title-main">Manganese heptoxide</span> Chemical compound

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Manganese(II) sulfate usually refers to the inorganic compound with the formula MnSO4·H2O. This pale pink deliquescent solid is a commercially significant manganese(II) salt. Approximately 260,000 tonnes of manganese(II) sulfate were produced worldwide in 2005. It is the precursor to manganese metal and many other chemical compounds. Manganese-deficient soil is remediated with this salt.

<span class="mw-page-title-main">Dithionate</span> Ion

The dithionate (or metabisulfate) anion, S
2
O2−
6
, is a sulfur oxoanion derived from dithionic acid, H2S2O6. Its chemical formula is sometimes written in a semistructural format, as [O3SSO3]2−. It is the first member of the polythionates.

<span class="mw-page-title-main">Cobalt(III) oxide</span> Chemical compound

Cobalt(III) oxide is the inorganic compound with the formula of Co2O3. Although only two oxides of cobalt are well characterized, CoO and Co3O4, procedures claiming to give Co2O3 have been described. Thus treatment of Co(II) salts such as cobalt(II) sulfate with an aqueous solution of sodium hypochlorite (also known as bleach) gives a black solid:

<span class="mw-page-title-main">Chromium(II) sulfate</span> Chemical compound

Chromium(II) sulfate is an inorganic compound with the chemical formula CrSO4. It often comes as hydrates CrSO4·nH2O. Several hydrated salts are known. The pentahydrate CrSO4·5H2O is a blue solid that dissolves readily in water. Solutions of chromium(II) are easily oxidized by air to Cr(III) species. Solutions of Cr(II) are used as specialized reducing agents of value in organic synthesis.

<span class="mw-page-title-main">Barium manganate</span> Chemical compound

Barium manganate is an inorganic compound with the formula BaMnO4. It is used as an oxidant in organic chemistry. It belongs to a class of compounds known as manganates in which the manganese resides in a +6 oxidation state. Manganate should not be confused with permanganate which contains manganese(VII). Barium manganate is a powerful oxidant, popular in organic synthesis and can be used in a wide variety of oxidation reactions.

Barium permanganate is a chemical compound, with the formula Ba(MnO4)2. It forms violet to brown crystals that are sparingly soluble in water.

References

  1. International Union of Pure and Applied Chemistry (2005). Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). Cambridge (UK): RSCIUPAC. ISBN   0-85404-438-8. p. 130. Electronic version.
  2. Perrin, D. D., ed. (1982) [1969]. Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution. IUPAC Chemical Data (2nd ed.). Oxford: Pergamon (published 1984). Entry 63. ISBN   0-08-029214-3. LCCN   82-16524.
  3. 1 2 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN   978-0-08-037941-8. pp. 715-716

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