Jump to content

Carbonyl bromide

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Smokefoot (talk | contribs) at 14:35, 9 November 2013 (Undid revision 580788393 by 79.243.242.208 (talk) pondering a concept vs reporting). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Carbonyl bromide[1]
Structural formula of carbonyl bromide
Structural formula of carbonyl bromide
Ball-and-stick model of carbonyl bromide
Ball-and-stick model of carbonyl bromide
Names
Other names
Bromophosgene, carbonic dibromide, carbonyl dibromide
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/CBr2O/c2-1(3)4 checkY
    Key: MOIPGXQKZSZOQX-UHFFFAOYSA-N checkY
  • InChI=1/CBr2O/c2-1(3)4
    Key: MOIPGXQKZSZOQX-UHFFFAOYAM
  • BrC(Br)=O
Properties
COBr2
Molar mass 187.818 g/mol
Appearance colorless liquid
Density 2.52 g/ml at 15°C
Boiling point 64.5°C
reacts with water
Thermochemistry
61.8 J·mol-1·K-1 (gas)
309.1 J·mol-1·K-1 (gas)
-127.2 kJ·mol-1 (liquid)
-96.2 kJ·mol-1 (gas)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
4
0
1
Related compounds
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 ?)

Carbonyl bromide, also known as bromophosgene by analogy to phosgene, is an organic chemical compound. It is a decomposition product of halon compounds used in fire extinguishers.[2]

Reactions

Carbonyl bromide is formed when carbon tetrabromide is melted and concentrated sulfuric acid is added. Even at low temperatures, carbonyl bromide decomposes to carbon monoxide and elemental bromine.[3]

References

  1. ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 3–96, 4–50, 5–26, ISBN 0-8493-0594-2
  2. ^ US Occupational Safety and Health Administration (May 1996). "Common Fire Extinguishing Agents". Retrieved 2009-11-21.
  3. ^ Katrizsky, Alan R.; Meth-Cohn, Otto; Wees, Charles W. (1995), Organic Functional Group Transformations, vol. 6, Elsevier, pp. 417–8, ISBN 978-0-08-042704-1, retrieved 2009-11-23