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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    Terminal alkynes have the formula RC≡CH, where at least one end of the alkyne is a hydrogen atom. An example is methylacetylene (propyne using IUPAC nomenclature). They are often prepared by alkylation of monosodium acetylide. [4] Terminal alkynes, like acetylene itself, are mildly acidic, with pK a values of around 25.

  3. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    In organic chemistry, terminal alkenes (alpha-olefins, α-olefins, or 1-alkenes) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula C x H 2x, distinguished by having a double bond at the primary, alpha (α), or 1-position. [1]

  4. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    A 3D model of ethylene, the simplest alkene. In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. [1] The double bond may be internal or in the terminal position.

  5. Transition metal alkyne complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkyne...

    Transition metal alkyne complexes are often formed by the displacement of labile ligands by the alkyne. For example, a variety of cobalt-alkyne complexes arise by the reaction of alkynes with dicobalt octacarbonyl. [2] Co 2 (CO) 8 + R 2 C 2 → (R 2 C 2)Co 2 (CO) 6 + 2 CO. Many alkyne complexes are produced by reduction of metal halides: [3]

  6. 1-Pentyne - Wikipedia

    en.wikipedia.org/wiki/1-Pentyne

    It is a terminal alkyne, in fact the smallest that is liquid at room temperature. The compound is a common terminal alkyne substrate in diverse studies of catalysis. The compound is a common terminal alkyne substrate in diverse studies of catalysis.

  7. Alkenylaluminium compounds - Wikipedia

    en.wikipedia.org/wiki/Alkenylaluminium_compounds

    Hydroaluminations of terminal alkynes typically produce terminal alkenylalanes as a result. Selectivity in hydroaluminations of internal alkynes is typically low, unless an electronic bias exists in the substrate (such as a phenyl ring in conjugation with the alkyne).

  8. 1-Butyne - Wikipedia

    en.wikipedia.org/wiki/1-Butyne

    It is a terminal alkyne. The compound is a common terminal alkyne substrate in diverse studies of catalysis. It is a colorless combustible gas. [1] 1-Butyne participates in reactions typical for terminal alkynes, such as alkyne metathesis, [2] hydrogenation, condensation with formaldehyde.

  9. 1-Decyne - Wikipedia

    en.wikipedia.org/wiki/1-Decyne

    1-Decyne is the organic compound with the formula C 8 H 17 C≡CH. It is a terminal alkyne.A colorless liquid, 1-decyne is used as a model substrate when evaluating methodology in organic synthesis.