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Sodium hypobromite

From Wikipedia, the free encyclopedia
Sodium hypobromite
Names
IUPAC name
Sodium hypobromite
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.034.096Edit this at Wikidata
EC Number
  • 237-520-4
UNII
  • InChI=1S/BrO.Na/c1-2;/q-1;+1
    Key: CRWJEUDFKNYSBX-UHFFFAOYSA-N
  • [O-]Br.[Na+]
Properties
NaOBr
Molar mass118.893 g·mol−1
Appearanceorange solid
Related compounds
Otheranions
Related compounds
Hypobromous acid
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Sodium hypobromite is aninorganic compound with thechemical formulaNaOBr. It is asodiumsalt ofhypobromous acid. It consists of sodiumcationsNa+ andhypobromiteanionsOBr. It is usually obtained as thepentahydrate, so the compound that is usually called sodium hypobromite actually has the formulaNaOBr·5H2O. It is a yellow-orange solid that is soluble in water. It adopts amonoclinic crystal structure with a Br–O bond length of 1.820 Å.[1] It is thebromine analogue ofsodium hypochlorite, the active ingredient in commonbleach. In practice the salt is usually encountered as anaqueous solution.

Sodium hypobromite arises by treatment of aqueous solution of bromine withbase:[2]

Br2 + 2 NaOH → NaBr + NaOBr + H2O

It can be preparedin situ for use as areagent, such as in the synthesis of3-aminopyridine fromnicotinamide[3] (Hofmann rearrangement).

Sodium hypobromite slowlydisproportionates tosodium bromide andsodium bromate:

3 NaOBr → 2 NaBr + NaBrO3

References

[edit]
  1. ^Topić, Filip; Marrett, Joseph M.; Borchers, Tristan H.; Titi, Hatem M.; Barrett, Christopher J.; Friščić, Tomislav (2021). "After 200 Years: The Structure of Bleach and Characterization of Hypohalite Ions by Single-Crystal X-Ray Diffraction".Angew. Chem. Int. Ed.60 (46):24400–24405.doi:10.1002/anie.202108843.PMID 34293249.S2CID 236199263.
  2. ^Schmeisser, M. (1963)."Sodium Hypobromite". In Brauer, Georg (ed.).Handbook of Preparative Inorganic Chemistry. Vol. 1 (2nd ed.). New York:Academic Press. pp. 310–311.ISBN 9780323161275.{{cite book}}:ISBN / Date incompatibility (help)
  3. ^Allen, C. F. H.; Wolf, Calvin N. (1950)."3-Aminopyridine".Organic Syntheses.30: 3.doi:10.15227/orgsyn.030.0003;Collected Volumes, vol. 4, p. 45.
Inorganic
Halides
Chalcogenides
Pnictogenides
Oxyhalides
Oxychalcogenides
Oxypnictogenides
Metalates
Others
Organic
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