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Hydrogen bromide

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Hydrogen bromide
Hydrogen bromide
Hydrogen bromide
Names
IUPAC name
Hydrogen bromide
Other names
Bromane
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.090 Edit this at Wikidata
EC Number
  • 233-113-0
RTECS number
  • MW3850000
UN number 1048
  • InChI=1S/BrH/h1H checkY
    Key: CPELXLSAUQHCOX-UHFFFAOYSA-N checkY
  • InChI=1/BrH/h1H
    Key: CPELXLSAUQHCOX-UHFFFAOYAZ
  • Br
Properties
HBr
Molar mass 80.91 g/mol
Appearance Colorless gas.
Density 3.307 g/L, gas.
Melting point –86.80 °C (186.35 K)
Boiling point –66.38 °C (206.77 K)
193 g/100 ml (20 °C)
Acidity (pKa) ≈ –9.5
1.325
Structure
Diatomic
0.82 D
Thermochemistry
0.3507 J/g K
-0.4486 kJ/g, -36.3 kJ/mol
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3
0
0
Related compounds
Other anions
Hydrogen fluoride,
Hydrogen chloride,
Hydrogen iodide
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 ?)

Hydrogen bromide is the diatomic molecule HBr. HBr is a gas at standard conditions. Hydrobromic acid forms upon dissolving HBr in water. Conversely, HBr can be liberated from hydrobromic acid solutions with the addition of a dehydration agent, but not by distillation. Hydrogen bromide and hydrobromic acid are, therefore, not the same, but they are related. Commonly, chemists refer to hydrobromic acid as "HBr", and this usage, while understood by most chemists, is imprecise and can be confusing to the non-specialist.

General description

At room temperature, HBr is a nonflammable gas with an acrid odor, fuming in moist air because of the formation of hydrobromic acid. HBr is very soluble in water, forming hydrobromic acid solution, which is saturated at 68.85% HBr by weight at room temperature. Aqueous solutions that are 47.38% HBr by weight form a constant-boiling mixture (reverse azeotrope) that boils at 126°C. Boiling less concentrated solutions releases H2O until the constant boiling mixture composition is reached.

Uses of HBr

There are many uses of HBr in chemical synthesis. For example, HBr is used for the production of alkyl bromides from alcohols:

ROH + HBr → RBr + H2O

HBr adds to alkenes to give bromoalkanes, an important family of organobromine compounds:

RCH=CH2 + HBr → RCH(Br)–CH3

HBr adds to alkynes to yield bromoalkenes. The stereochemistry of this type of addition is usually anti:

RC≡CH + HBr → RC(Br)=CH2

HBr adds to the haloalkene to form a geminal dihaloalkane. (This type of addition follows Markovnikov's rule):

RC(Br)=CH2 + HBr → RC(Br2)–CH3

Also, HBr is used to open epoxides and lactones and in the synthesis of bromoacetals. Additionally, HBr catalyzes many organic reactions.[1][2][3][4]

Industrial preparation

Hydrogen bromide (along with hydrobromic acid) is produced on a much smaller scale than the corresponding chlorides. In the primary industrial preparation, hydrogen and bromine are combined at temperatures 200-400 °C. The reaction is typically catalyzed by platinum or asbestos.[2][5]

Laboratory synthesis

HBr can be synthesized by a variety of methods. A convenient laboratory synthesis entails the reaction between strong acids and NaBr:[6] Sulfuric acid is ineffective because HBr formed will be oxidized to bromine gas:

2 HBr + H2SO4 → Br2 + SO2 + 2H2O

Non-oxidising acids like phosphoric acid can be used for the purpose. Alternatively, it can be prepared by the bromination of tetraline (1,2,3,4-tetrahydronaphthalene):[6]

C10H12 + 4 Br2 → C10H8Br4 + 4 HBr

Alternatively bromine can be reduced with phosphorous acid:[2]

Br2 + H3PO3 + H2O → H3PO4 + 2 HBr

Anhydrous hydrogen bromide can also be produced on a small scale by thermolysis of triphenylphosphonium bromide in refluxing xylene.[1]

HBr prepared by the above methods can be contaminated with Br2, which can be removed by passing the gas through Cu turnings or through phenol.[5]

References

  1. ^ a b Hercouet, A.;LeCorre, M. (1988) Triphenylphosphonium bromide: A convenient and quantitative source of gaseous hydrogen bromide. Synthesis, 157-158.
  2. ^ a b c Greenwood, N. N.; Earnshaw, A. Chemistry of the Elements; Butterworth-Heineman: Oxford, Great Britain; 1997; pp. 809-812.
  3. ^ Carlin, William W. U.S. patent 4,147,601, April 3, 1979
  4. ^ Vollhardt, K. P. C.; Schore, N. E. Organic Chemistry: Structure and Function; 4th Ed.; W. H. Freeman and Company: New York, NY; 2003.
  5. ^ a b Ruhoff, J. R.; Burnett, R. E.; Reid, E. E. "Hydrogen Bromide (Anhydrous)" Organic Syntheses, Vol. 15, p.35 (Coll. Vol. 2, p.338).
  6. ^ a b WebElements: Hydrogen Bromide