Chromyl chloride

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Chromyl chloride
Wireframe model of chromyl chloride
Wireframe model of chromyl chloride
Ball and stick model of chromyl chloride
Ball and stick model of chromyl chloride
Chromyl chloride in vial
Names
Preferred IUPAC name
Chromium(VI) dichloride dioxide
Systematic IUPAC name
Dichlorodioxochromium
Other names
Chromic acid chloride

Chromium oxychloride

Etard Reagent
Chlorochromic anhydride
Chromic oxychloride
Chromium chloride oxide
Chromium dioxide dichloride
Chromium dioxychloride
Chromium oxychloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.035.491 Edit this at Wikidata
EC Number
  • 239-056-8
RTECS number
  • GB5775000
UNII
  • InChI=1S/2ClH.Cr.2O/h2*1H;;;/q;;+2;;/p-2 checkY
    Key: AHXGRMIPHCAXFP-UHFFFAOYSA-L checkY
  • InChI=1S/2ClH.Cr.2O/h2*1H;;;/q;;+2;;/p-2
    Key: AHXGRMIPHCAXFP-UHFFFAOYSA-L
  • InChI=1/2ClH.Cr.2O/h2*1H;;;/q;;+2;;/p-2/rCl2CrO2/c1-3(2,4)5
    Key: AHXGRMIPHCAXFP-GRYJOLFGAD
  • Cl[Cr](Cl)(=O)=O
Properties
CrO2Cl2
Molar mass 154.9008 g/mol
Appearance blood red fuming liquid, similar to bromine
Odor musty, burning, acrid[1]
Density 1.911 g/mL, liquid
Melting point -96.5 °C
Boiling point 117 °C
Very soluble,hydrolysis
Vapor pressure 20 mmHg (20 °C)[1]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
carcinogen, reacts violently with water[1]
GHS labelling:
GHS03: OxidizingGHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard[2]
NFPA 704 (fire diamond)
Flash point noncombustible [1]
NIOSH (US health exposure limits):
PEL (Permissible)
none[1]
REL (Recommended)
Ca TWA 0.001 mg Cr(VI)/m3[1]
IDLH (Immediate danger)
N.D.[1]
Related compounds
Related compounds
SO2Cl2; VOCl3; MoO2Cl2; WO2Cl2; CrO2F2
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Chromyl chloride is a reddish-brown compound of chromium with oxygen and chlorine. The compound is extremely corrosive and will readily generate reddish brown fumes in air. Like most Chromium(VI) compounds, it is also highly carcinogenic.

Preparation

Chromyl chloride can be prepared by the reaction of potassium chromate or potassium dichromate with hydrogen chloride in the presence of sulfuric acid, followed by gentle distillation.[3][4]

K2Cr2O7 + 6 HCl → 2 CrO2Cl2 + 2 KCl + 3 H2O

The sulfuric acid serves as the dehydration agent. It can also be prepared directly by exposing chromium trioxide to anhydrous hydrogen chloride gas.

CrO3 + 2 HCl ⇌ CrO2Cl2 + H2O

The method used to prepare chromyl chloride is the basis for a qualitative test for chloride: a sample suspected of containing chloride is heated with a mixture of potassium dichromate and concentrated sulfuric acid. If chloride is present, chromyl chloride forms as evidenced by red fumes of CrO2Cl2. Analogous compounds are not formed with fluorides, bromides, iodides and cyanides.

Reagent for oxidation of alkenes

Chromyl chloride oxidizes internal alkenes to alpha-chloroketones or related derivatives.[5] It will also attack benzylic methyl groups to give aldehydes via the Étard reaction. Dichloromethane is a suitable solvent for these reactions.[6]

Safety considerations

CrO2Cl2 hydrolyzes to release hydrochloric acid (HCl) and hexavalent chromium (CrVI)

Acute: Exposure to chromyl chloride vapour irritates the respiratory system and severely irritates the eyes, and the liquid burns the skin and eyes. Ingestion would cause severe internal damage.[7]

Chronic: CrVI can produce chromosomal aberrations and is a human carcinogen via inhalation.[8] Frequent exposure of the skin to chromyl chloride may result in ulceration.[7]

References

  1. ^ a b c d e f g NIOSH Pocket Guide to Chemical Hazards. "#0142". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ [1]
  3. ^ Moody, B.J. (1965). "22". Comparative Inorganic Chemistry (1 ed.). London: Edward Arnold. p. 381. ISBN 0-7131-3679-0.
  4. ^ Sisler, Harry H. (1946). "Chromyl Chloride [Chromium(VI) Dioxychloride]". Inorganic Syntheses. 2: 205–207. doi:10.1002/9780470132333.ch63.
  5. ^ Freeman, Fillmore; DuBois, Richard H.; McLaughlin, Thomas G. (1971). "Aldehydes by Oxidation of Terminal Olefins with Chromyl Chloride: 2,4,4-Trimethylpentanal". Org. Synth. 51: 4. doi:10.15227/orgsyn.051.0004.
  6. ^ F. Freeman (2004). "Chromyl Chloride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rc177..}}
  7. ^ a b Prof CH Gray, ed. (1966). "IV". Laboratory Handbook of Toxic Agents (2 ed.). London: Royal Institute of Chemistry. p. 79.
  8. ^ IARC (1999-11-05) [1990]. Volume 49: Chromium, Nickel, and Welding (PDF). pp. 21–23. ISBN 92-832-1249-5. Archived from the original (PDF) on 2008-12-24. Retrieved 2008-03-26.

External links