Tetrahalomethane

Class of chemical compounds

Tetrahalomethanes are fully halogenated methane derivatives of general formula CFkCllBrmInAtp, where:

k + l + m + n + p = 4 {\displaystyle k+l+m+n+p=4}
Tetrahalomethanes are on the border of inorganic and organic chemistry, thus they can be assigned both inorganic and organic names by IUPAC: tetrafluoromethane - carbon tetrafluoride, tetraiodomethane - carbon tetraiodide, dichlorodifluoromethane - carbon dichloride difluoride.

Each halogen (F, Cl, Br, I, At) forms a corresponding halomethane, but their stability decreases in order CF4 > CCl4 > CBr4 > CI4 from exceptionally stable gaseous tetrafluoromethane with bond energy 515 kJ·mol−1 to solid tetraiodomethane, depending on bond energy.

Many mixed halomethanes are also known, such as CBrClF2.

Uses

Fluorine, chlorine, and sometimes bromine-substituted halomethanes were used as refrigerants, commonly known as CFCs (chlorofluorocarbons).

See also

  • v
  • t
  • e
Unsubstituted
  • CH4
Monosubstituted
  • CH3F
  • CH3Cl
  • CH3Br
  • CH3I
  • CH3At
Disubstituted
  • CH2F2
  • CH2ClF
  • CH2BrF
  • CH2FI
  • CH2Cl2
  • CH2BrCl
  • CH2ClI
  • CH2Br2
  • CH2BrI
  • CH2I2
Trisubstituted
  • CHF3
  • CHClF2
  • CHBrF2
  • CHF2I
  • CHCl2F
  • C*HBrClF
  • C*HClFI
  • CHBr2F
  • C*HBrFI
  • CHFI2
  • CHCl3
  • CHBrCl2
  • CHCl2I
  • CHBr2Cl
  • C*HBrClI
  • CHClI2
  • CHBr3
  • CHBr2I
  • CHBrI2
  • CHI3
Tetrasubstituted
  • CF4
  • CClF3
  • CBrF3
  • CF3I
  • CCl2F2
  • CBrClF2
  • CClF2I
  • CBr2F2
  • CBrF2I
  • CF2I2
  • CCl3F
  • CBrCl2F
  • CCl2FI
  • CBr2ClF
  • C*BrClFI
  • CClFI2
  • CBr3F
  • CBr2FI
  • CBrFI2
  • CFI3
  • CCl4
  • CBrCl3
  • CCl3I
  • CBr2Cl2
  • CBrCl2I
  • CCl2I2
  • CBr3Cl
  • CBr2ClI
  • CBrClI2
  • CClI3
  • CBr4
  • CBr3I
  • CBr2I2
  • CBrI3
  • CI4
* Chiral compound.