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  2. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    Carbon tetrachloride, also known by many other names (such as carbon tet for short and tetrachloromethane, also recognised by the IUPAC), is a chemical compound with the chemical formula CCl 4. It is a non-flammable, dense, colourless liquid with a "sweet" chloroform-like odour that can be detected at low levels.

  3. Molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Molecular_geometry

    Molecular geometry is the three-dimensional arrangement of the atoms that constitute a molecule. It includes the general shape of the molecule as well as bond lengths , bond angles , torsional angles and any other geometrical parameters that determine the position of each atom.

  4. Carbon tetrachloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride_(data...

    Structure and properties Index of refraction, n D: 1.460 Abbe number? Dielectric constant, ε r: 2.2379 ε 0 at 20 °C : Bond strength? Bond length: 175pm Bond angle: 109.5° Cl–C–Cl

  5. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron. The bond angles are arccos (− ⁠ 1 / 3 ⁠ ) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane ( CH 4 ) [ 1 ] [ 2 ] as well as its heavier analogues .

  6. Chloroform - Wikipedia

    en.wikipedia.org/wiki/Chloroform

    Chloroform undergoes further chlorination to yield carbon tetrachloride (CCl 4): CHCl 3 + Cl 2 → CCl 4 + HCl The output of this process is a mixture of the four chloromethanes: chloromethane , methylene chloride (dichloromethane), trichloromethane (chloroform), and tetrachloromethane (carbon tetrachloride).

  7. Gauche effect - Wikipedia

    en.wikipedia.org/wiki/Gauche_effect

    The gauche effect is very sensitive to solvent effects, due to the large difference in polarity between the two conformers.For example, 2,3-dinitro-2,3-dimethylbutane, which in the solid state exists only in the gauche conformation, prefers the gauche conformer in benzene solution by a ratio of 79:21, but in carbon tetrachloride, it prefers the anti conformer by a ratio of 58:42. [9]

  8. Boron trichloride - Wikipedia

    en.wikipedia.org/wiki/Boron_trichloride

    Colourless diboron tetrachloride (m.p. -93 °C) is a planar molecule in the solid, (similar to dinitrogen tetroxide, but in the gas phase the structure is staggered. [4] It decomposes (disproportionates) at room temperatures to give a series of monochlorides having the general formula (BCl) n, in which n may be 8, 9, 10, or 11.

  9. Thiophosgene - Wikipedia

    en.wikipedia.org/wiki/Thiophosgene

    Thiophosgene decomposes at 200 °C or above to form carbon disulfide and carbon tetrachloride. [9] It has also been observed decomposing to hydrogen sulfide, hydrogen chloride, and carbonyl sulfide gases via contact with human tissue. [10] [failed verification]