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  2. 1-Butyne - Wikipedia

    en.wikipedia.org/wiki/1-Butyne

    1-Butyne is an organic compound with the formula CH 3 CH 2 C≡CH.It is a terminal alkyne.The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas.

  3. Acetylene - Wikipedia

    en.wikipedia.org/wiki/Acetylene

    Acetylene (systematic name: ethyne) is the chemical compound with the formula C 2 H 2 and structure H−C≡C−H. It is a hydrocarbon and the simplest alkyne. [8] This colorless gas is widely used as a fuel and a chemical building block. It is unstable in its pure form and thus is usually handled as a solution. [9]

  4. 2-Butyne - Wikipedia

    en.wikipedia.org/wiki/2-butyne

    Symmetry analysis using the Molecular Symmetry Group [4] [5] G 36 shows that one would need to analyse its high resolution rotation-vibration Raman spectrum to determine its equilibrium structure. 2-Butyne ( dimethylethyne ) forms with 5-decyne ( dibutylethyne ), 4-octyne ( dipropylethyne ) and 3-hexyne ( diethylethyne ) a group of symmetric ...

  5. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    A 3D model of ethyne (), the simplest alkyneIn organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. [1] The simplest acyclic alkynes with only one triple bond and no other functional groups form a homologous series with the general chemical formula C n H 2n−2.

  6. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2.It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. [7] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds).

  7. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    An example of a simple chain reaction is the thermal decomposition of acetaldehyde (CH 3 CHO) to methane (CH 4) and carbon monoxide (CO). The experimental reaction order is 3/2, [4] which can be explained by a Rice-Herzfeld mechanism. [5] This reaction mechanism for acetaldehyde has 4 steps with rate equations for each step :

  8. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    In the following reaction (scheme 1), the alkyne proton of ethyl propiolate is deprotonated by n-butyllithium at -78 °C to form lithium ethyl propiolate to which cyclopentanone is added forming a lithium alkoxide. Acetic acid is added to remove lithium and liberate the free alcohol. [6] Scheme 1.

  9. Butyne - Wikipedia

    en.wikipedia.org/wiki/Butyne

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