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  2. Triphenylmethyl chloride - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_chloride

    Molar mass: 278.7754 g/mol Appearance white to yellow solid ... Triphenylmethyl chloride or trityl chloride (TrCl) is a white solid with the chemical formula C 19 H ...

  3. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    Triphenylmethane was first synthesized in 1872 by the German chemist August Kekulé and his Dutch student Antoine Paul Nicolas Franchimont (1844–1919) by heating diphenylmercury (Hg(C 6 H 5) 2, Quecksilberdiphenyl) with benzal chloride (C 6 H 5 CHCl 2, Benzylenchlorid).

  4. Triphenylmethanol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanol

    Triphenylmethanol features three phenyl (Ph) rings and an alcohol group bound to a central tetrahedral carbon atom. All three C–Ph bonds are typical of sp 3-sp 2 carbon-carbon bonds with lengths of approximately 1.47 Å, while the C–O bond length is approximately 1.42 Å.

  5. Molar mass - Wikipedia

    en.wikipedia.org/wiki/Molar_mass

    The molar mass of atoms of an element is given by the relative atomic mass of the element multiplied by the molar mass constant, M u ≈ 1.000 000 × 10 −3 kg/mol ≈ 1 g/mol. For normal samples from Earth with typical isotope composition, the atomic weight can be approximated by the standard atomic weight [ 2 ] or the conventional atomic weight.

  6. Triphenylmethanethiol - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethanethiol

    It is the thiol derivative of the bulky substituent triphenylmethyl (called trityl). [1] [2] The compound forms a number of unusual derivatives that are more stable than less bulky analogues. The sulfenyl chloride (C 6 H 5) 3 CSCl is obtained from the thiol with sulfuryl chloride. It in turn reacts with ammonia to form the sulfenamide (C 6 H 5 ...

  7. Triphenylmethyl radical - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_radical

    The triphenylmethyl radical can be prepared by homolysis of triphenylmethyl chloride 1 by a metal like silver or zinc in benzene or diethyl ether. The radical 2 forms a chemical equilibrium with the quinoid-type dimer 3 (Gomberg's dimer). In benzene the concentration of the radical is 2%. [3] Triphenylmethyl radical

  8. Triphenylcarbenium - Wikipedia

    en.wikipedia.org/wiki/Triphenylcarbenium

    Triphenylcarbenium Space-filling model of the Ph 3 C + ion. In chemistry, triphenylcarbenium, [1] triphenylmethyl cation, tritylium , [2] or trityl cation is an ion with formula [C 19 H 15] + or (C 6 H 5) 3 C +, consisting of a carbon atom with a positive charge connected to three phenyl groups.

  9. Tropylium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tropylium_tetrafluoroborate

    Tropylium tetrafluoroborate is an organic compound with the formula [C 7 H 7] + [BF 4] −.Containing the tropylium cation and the non-coordinating tetrafluoroborate counteranion, tropylium tetrafluoroborate is a rare example of a readily isolable carbocation.