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  2. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    Ethane (US: / ˈ ɛ θ eɪ n / ETH-ayn, UK: / ˈ iː θ eɪ n / EE-thayn) is a naturally occurring organic chemical compound with chemical formula C 2 H 6. At standard temperature and pressure, ethane is a colorless, odorless gas. Like many hydrocarbons, ethane is isolated on an industrial scale from natural gas and as a petrochemical by ...

  3. Ethane (data page) - Wikipedia

    en.wikipedia.org/wiki/Ethane_(data_page)

    crystal I → liquid 14.703 kJ/mol at −89.0 °C Std entropy change of vaporization, Δ vap S o crystal I → liquid 79.87 J/(mol·K) at −89.0 °C Std enthalpy change of state transition, Δ trs H o crystal II → crystal I 2.282 kJ/mol at −183.3 °C Std entropy change of state transition, Δ trs S o crystal II → crystal I 25.48 kJ/mol ...

  4. Ethanethiol - Wikipedia

    en.wikipedia.org/wiki/Ethanethiol

    It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of EtSH is infamous. Ethanethiol is more volatile than ethanol due to a diminished ability to engage in hydrogen ...

  5. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    When ethane is the feedstock, ethylene is the product. Ethylene is separated from the resulting mixture by repeated compression and distillation . [ 17 ] In Europe and Asia, ethylene is obtained mainly from cracking naphtha, gasoil and condensates with the coproduction of propylene, C4 olefins and aromatics (pyrolysis gasoline). [ 29 ]

  6. Ethane-1,2-dithiol - Wikipedia

    en.wikipedia.org/wiki/Ethane-1,2-dithiol

    Ethane-1,2-dithiol, also known as EDT, [1] is a colorless liquid with the formula C 2 H 4 2. It has a very characteristic odor which is compared by many people to rotten cabbage . It is a common building block in organic synthesis and an excellent ligand for metal ions.

  7. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    pKa values for acetic, chloroacetic, dichloroacetic and trichloroacetic acids. Inductive effects and mesomeric effects affect the pK a values. A simple example is provided by the effect of replacing the hydrogen atoms in acetic acid by the more electronegative chlorine atom.

  8. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  9. Acetamide - Wikipedia

    en.wikipedia.org/wiki/Acetamide

    Acetamide (systematic name: ethanamide) is an organic compound with the formula CH 3 CONH 2.It is an amide derived from ammonia and acetic acid.It finds some use as a plasticizer and as an industrial solvent. [5]