Difference between revisions of "Trichloroethylene"

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===Relevant Sciencemadness threads===
 
===Relevant Sciencemadness threads===
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[[Category:Chemical compounds]]
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[[Category:Organic compounds]]
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[[Category:Organochlorine compounds]]
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[[Category:Haloalkanes]]
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[[Category:Solvents]]
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[[Category:Nonpolar solvents]]
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[[Category:Readily available chemicals]]
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[[Category:Volatile chemicals]]
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[[Category:Carcinogenic]]

Revision as of 09:03, 21 September 2015

Trichloroethylene , also known as trichloroethene is an organic compound, a haloalkene with the chemical formula ClCHCCl2.

Properties

Chemical

Trichloroethylene is unstable in the presence of a metal over prolonged exposure.

Physical

Trichloroethylene is a clear non-flammable liquid with a sweet smell. It melts at −73 °C and boils at 87.2 °C.

Availability

Delete this section if not applicable

Preparation

Trichloroethylene can be synthesized by chlorinating ethylene over a ferric chloride catalyst to produce 1,2-dichloroethane, which is heated to 400 °C with additional chlorine, to yield trichloroethylene.

CH2=CH2 + Cl2 → ClCH2CH2Cl
ClCH2CH2Cl + 2 Cl2 → ClCH=CCl2 + 3 HCl

Projects

  • Extract caffeine
  • Make chloroacetic acid

Handling

Safety

Storage

Disposal

References

Relevant Sciencemadness threads