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| ImageFile1 = Sulfurous-acid-3D-balls.png
| ImageFile1 = Sulfurous-acid-3D-balls.png
| ImageName1 = Ball-and-stick model of sulfurous acid
| ImageName1 = Ball-and-stick model of sulfurous acid
| OtherNames =
| OtherNames = Sulfuric(IV) acid<br/>Thionic acid<br/>Sulfinic acid
| IUPACName = Sulfurous acid
| IUPACName = Sulfurous acid
| SystematicName =
| SystematicName =
| Section1 = {{Chembox Identifiers
| Section1 = {{Chembox Identifiers
| CASNo = 7782-99-2
| CASNo_Ref = {{cascite|correct|CAS}}
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 48854
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1161699
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 1069
| ChemSpiderID = 1069
| EC_number = 231-973-1
| Gmelin = 1458
| PubChem = 1100
| PubChem = 1100
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII_Ref = {{fdacite|correct|FDA}}
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| InChI = 1/H2O3S/c1-4(2)3/h(H2,1,2,3)
| InChI = 1/H2O3S/c1-4(2)3/h(H2,1,2,3)
| InChIKey = LSNNMFCWUKXFEE-UHFFFAOYAJ
| InChIKey = LSNNMFCWUKXFEE-UHFFFAOYAJ
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 48854
| SMILES = O[S](=O)O
| SMILES = O[S](=O)O
| SMILES1 = O[S+](O)[O-]
| SMILES1 = O[S+](O)[O-]
| SMILES1_Comment = Tautomer
| SMILES1_Comment = Tautomer
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1161699
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/H2O3S/c1-4(2)3/h(H2,1,2,3)
| StdInChI = 1S/H2O3S/c1-4(2)3/h(H2,1,2,3)
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = LSNNMFCWUKXFEE-UHFFFAOYSA-N
| StdInChIKey = LSNNMFCWUKXFEE-UHFFFAOYSA-N
| CASNo = 7782-99-2
| CASNo_Ref = {{cascite|correct|CAS}}
}}
}}
| Section2 = {{Chembox Properties
| Section2 = {{Chembox Properties
| Formula = H<sub>2</sub>SO<sub>3</sub>
| Formula = {{chem2|H2SO3}}
| MolarMass = 82.07 g/mol
| MolarMass = 82.07 g/mol
| ConjugateBase = [[Bisulfite]]
| ConjugateBase = [[Bisulfite]]
| pKa = 1.857, 7.172<ref name=P82db>{{cite book|title=Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution|editor-first=D.&nbsp;D.|editor-last=Perrin|edition=2nd|series=[[IUPAC]] Chemical Data|issue=29|publisher=Pergamon|location=Oxford|year=1982|publication-date=1984|orig-date=1969|lccn=82-16524|isbn=0-08-029214-3|at=Entry&nbsp;217}}</ref>
| pKa = 1.857, 7.172
}}
}}
| Section3 =
| Section3 =
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| Section7 = {{Chembox Hazards
| Section7 = {{Chembox Hazards
| ExternalSDS = [http://www.inchem.org/documents/icsc/icsc/eics0074.htm ICSC 0074]
| ExternalSDS = [http://www.inchem.org/documents/icsc/icsc/eics0074.htm ICSC 0074]
| GHSPictograms = {{GHS05}}{{GHS07}}
| EUClass = {{Hazchem C}} ('''C''')
| GHSSignalWord = Danger
| RPhrases = {{R20}}, {{R34}}
| HPhrases = {{H-phrases|314|332}}
| SPhrases = {{S1/2}}, {{S9}}, {{S26}}, {{S36/37/39}}, {{S45}}
| PPhrases = {{P-phrases|260|261|264|271|280|301+330+331|303+361+353|304+312|304+340|305+351+338|310|312|321|363|405|501}}
| FlashPt = Non-flammable
| FlashPt = Non-flammable
}}
}}
| Section8 = {{Chembox Related
| Section8 = {{Chembox Related
| OtherCompounds = [[Sulfur dioxide]]<br/>[[Sulfuric acid]]
| OtherCompounds = [[Sulfur dioxide]]<br/>[[Sulfuric acid]]<br/>[[Selenous acid]]
}}
}}
}}
}}


'''Sulfuric(IV) acid''' ([[United Kingdom]] spelling: '''sulphuric(IV) acid'''), also known as '''sulfurous''' (UK:&nbsp;'''sulphurous''') '''acid''' and '''thionic acid''',{{citation needed|date=July 2023}} is the [[chemical compound]] with the [[chemical formula|formula]] {{chem2|H2SO3}}.
'''Sulfurous acid''' (also '''Sulfuric(IV) acid''', '''Sulphuric acid (UK)''', '''Sulphuric(IV) acid''') is the [[chemical compound]] with the [[chemical formula|formula]] H<sub>2</sub>SO<sub>3</sub>. There is no evidence that sulfurous acid exists in solution, but the molecule has been detected in the gas phase.<ref>{{cite journal |author1=D. Sülzle |author2=M. Verhoeven |author3=J. K. Terlouw |author4=H. Schwarz | title = Generation and Characterization of Sulfurous Acid (H<sub>2</sub>SO<sub>3</sub>) and of Its Radical Cation as Stable Species in the Gas Phase | journal = [[Angew. Chem. Int. Ed. Engl.]] | volume = 27 | pages = 1533–4 | year = 1988 | doi = 10.1002/anie.198815331 | issue = 11}}</ref> The conjugate bases of this elusive acid are, however, common anions, [[bisulfite]] (or hydrogen sulfite) and [[sulfite]]. Sulfurous acid is an intermediate species in the formation of [[acid rain]] from sulfur dioxide.<ref>{{cite book|last1=McQuarrie |last2= Rock |date=1987 |title=General Chemistry |edition=2nd |publisher=W.H. Freeman and Company |location=New York |page=243 |ISBN=0-7167-1806-5}}</ref>

[[Raman spectroscopy|Raman spectra]] of solutions of [[sulfur dioxide]] in water show only signals due to the {{chem2|SO2}} molecule and the bisulfite ion, {{chem2|HSO3−}}.<ref>{{Jolly2nd}}</ref> The intensities of the signals are consistent with the following [[chemical equilibrium|equilibrium]]:

{{block indent|1={{chem2|SO2 + H2O ⇌ HSO3− + H+}}{{spaces|10}}''K''<sub>a</sub> = 1.54{{e|−2}}; p''K''<sub>a</sub> = 1.81.}}


[[Raman spectroscopy|Raman spectra]] of solutions of [[sulfur dioxide]] in water show only signals due to the SO<sub>2</sub> molecule and the bisulfite ion, {{chem|HSO|3|}}.<ref>{{Jolly2nd}}</ref> The intensities of the signals are consistent with the following [[chemical equilibrium|equilibrium]]:
::SO<sub>2</sub> + H<sub>2</sub>O {{eqm}} {{chem|HSO|3|−}} + H<sup>+</sup>{{spaces|10}}''K''<sub>a</sub> = 1.54{{e|−2}}; p''K''<sub>a</sub> = 1.81.
<sup>17</sup>O [[NMR spectroscopy]] provided evidence that solutions of sulfurous acid and protonated sulfites contain a mixture of isomers, which is in equilibrium:<ref name="InorgChem">{{cite book
<sup>17</sup>O [[NMR spectroscopy]] provided evidence that solutions of sulfurous acid and protonated sulfites contain a mixture of isomers, which is in equilibrium:<ref name="InorgChem">{{cite book
| title = Inorganic Chemistry, 3rd Edition
| title = Inorganic Chemistry, 3rd Edition
Line 73: Line 78:
| page = 520
| page = 520
}}</ref>
}}</ref>

: [H–OSO<sub>2</sub>]<sup>−</sup> ⇌ [H–SO<sub>3</sub>]<sup>−</sup>
{{block indent|{{chem2|[H\sOSO2]− ⇌ [H\sSO3]−}}}}
When trying to concentrate the solution by evaporation to produce waterless sulfurous acid it will decompose (reversing the forming reaction). In cooling down a [[clathrate]] SO<sub>2</sub>·{{frac|5|3|4}}H<sub>2</sub>O will crystallise which decomposes again at 7&nbsp;°C. Thus sulfurous acid H<sub>2</sub>SO<sub>3</sub> cannot be isolated.

Attempts to concentrate the solutions of sulfurous acid simply reverses the equilibrium, producing sulfur dioxide and water vapor. A [[clathrate]] with the formula {{chem2|4SO2*23H2O}} has been crystallised. It decomposes above 7&nbsp;°C.

==History and production==
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.<ref>{{Greenwood&Earnshaw2nd|page=719}}</ref> However, the molecule has been detected in the gas phase in 1988 by the dissociative ionization of [[diethyl sulfite]].<ref>{{cite journal |author1=D. Sülzle |author2=M. Verhoeven |author3=J. K. Terlouw |author4=H. Schwarz | title = Generation and Characterization of Sulfurous Acid (H<sub>2</sub>SO<sub>3</sub>) and of Its Radical Cation as Stable Species in the Gas Phase | journal = [[Angew. Chem. Int. Ed. Engl.]] | volume = 27 | pages = 1533–4 | year = 1988 | doi = 10.1002/anie.198815331 | issue = 11}}</ref> The conjugate bases of this elusive acid are, however, common anions, [[bisulfite]] (or hydrogen sulfite) and [[sulfite]]. Sulfurous acid is an intermediate species in the formation of [[acid rain]] from sulfur dioxide.<ref>{{cite book|last1=McQuarrie |last2= Rock |date=1987 |title=General Chemistry |edition=2nd |publisher=W.H. Freeman and Company |location=New York |page=243 |ISBN=0-7167-1806-5}}</ref>


==Uses==
==Uses==
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==References==
==References==
{{reflist}}
<references/>


{{Hydrogen compounds}}
{{Hydrogen compounds}}
{{Sulfites}}
{{sulfur compounds}}
{{Authority control}}
{{Authority control}}


[[Category:Hydrogen compounds]]
[[Category:Oxoacids]]
[[Category:Sulfites]]
[[Category:Sulfites]]
[[Category:Sulfur oxoacids]]
[[Category:Sulfur oxoacids]]
[[Category:Hypothetical chemical compounds]]

Latest revision as of 13:28, 13 December 2024

Sulfurous acid
Sulfuric(IV) acid
Ball-and-stick model of sulfurous acid
Names
IUPAC name
Sulfurous acid
Other names
Sulfuric(IV) acid
Thionic acid
Sulfinic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.029.066 Edit this at Wikidata
EC Number
  • 231-973-1
1458
KEGG
UNII
  • InChI=1S/H2O3S/c1-4(2)3/h(H2,1,2,3) checkY
    Key: LSNNMFCWUKXFEE-UHFFFAOYSA-N checkY
  • InChI=1/H2O3S/c1-4(2)3/h(H2,1,2,3)
    Key: LSNNMFCWUKXFEE-UHFFFAOYAJ
  • O[S](=O)O
  • Tautomer: O[S+](O)[O-]
Properties
H2SO3
Molar mass 82.07 g/mol
Acidity (pKa) 1.857, 7.172[1]
Conjugate base Bisulfite
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H314, H332
P260, P261, P264, P271, P280, P301+P330+P331, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P363, P405, P501
Flash point Non-flammable
Safety data sheet (SDS) ICSC 0074
Related compounds
Related compounds
Sulfur dioxide
Sulfuric acid
Selenous acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Sulfuric(IV) acid (United Kingdom spelling: sulphuric(IV) acid), also known as sulfurous (UK: sulphurous) acid and thionic acid,[citation needed] is the chemical compound with the formula H2SO3.

Raman spectra of solutions of sulfur dioxide in water show only signals due to the SO2 molecule and the bisulfite ion, HSO3.[2] The intensities of the signals are consistent with the following equilibrium:

SO2 + H2O ⇌ HSO3 + H+          Ka = 1.54×10−2; pKa = 1.81.

17O NMR spectroscopy provided evidence that solutions of sulfurous acid and protonated sulfites contain a mixture of isomers, which is in equilibrium:[3]

[H−OSO2] ⇌ [H−SO3]

Attempts to concentrate the solutions of sulfurous acid simply reverses the equilibrium, producing sulfur dioxide and water vapor. A clathrate with the formula 4SO2·23H2O has been crystallised. It decomposes above 7 °C.

History and production

[edit]

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] The conjugate bases of this elusive acid are, however, common anions, bisulfite (or hydrogen sulfite) and sulfite. Sulfurous acid is an intermediate species in the formation of acid rain from sulfur dioxide.[6]

Uses

[edit]

Aqueous solutions of sulfur dioxide, which sometimes are referred to as sulfurous acid, are used as reducing agents and as disinfectants, as are solutions of bisulfite and sulfite salts. They are oxidised to sulfuric acid or sulfate by accepting another oxygen atom.[7]

See also

[edit]

References

[edit]
  1. ^ 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 217. ISBN 0-08-029214-3. LCCN 82-16524.
  2. ^ Jolly, William L. (1991). Modern Inorganic Chemistry (2nd ed.). New York: McGraw-Hill. ISBN 0-07-032768-8.
  3. ^ Catherine E. Housecroft; Alan G. Sharpe (2008). "Chapter 16: The group 16 elements". Inorganic Chemistry, 3rd Edition. Pearson. p. 520. ISBN 978-0-13-175553-6.
  4. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 719. ISBN 978-0-08-037941-8.
  5. ^ D. Sülzle; M. Verhoeven; J. K. Terlouw; H. Schwarz (1988). "Generation and Characterization of Sulfurous Acid (H2SO3) and of Its Radical Cation as Stable Species in the Gas Phase". Angew. Chem. Int. Ed. Engl. 27 (11): 1533–4. doi:10.1002/anie.198815331.
  6. ^ McQuarrie; Rock (1987). General Chemistry (2nd ed.). New York: W.H. Freeman and Company. p. 243. ISBN 0-7167-1806-5.
  7. ^ L. Kolditz, Anorganische Chemie, VEB Deutscher Verlag der Wissenschaften, Berlin 1983, S. 476.