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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/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. Terminal alkenes are also known as α-olefins. The International Union of Pure and Applied Chemistry (IUPAC) recommends using the name "alkene" only for acyclic hydrocarbons ...

  3. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    Terminal alkynes, like acetylene itself, are mildly acidic, with pK a values of around 25. They are far more acidic than alkenes and alkanes, which have pK a values of around 40 and 50, respectively. The acidic hydrogen on terminal alkynes can be replaced by a variety of groups resulting in halo-, silyl-, and alkoxoalkynes.

  4. Alkyne metathesis - Wikipedia

    en.wikipedia.org/wiki/Alkyne_metathesis

    Alkyne metathesis. Alkyne metathesis is an organic reaction that entails the redistribution of alkyne chemical bonds. The reaction requires metal catalysts. Mechanistic studies show that the conversion proceeds via the intermediacy of metal alkylidyne complexes. [1][2][3] The reaction is related to olefin metathesis.

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkane. In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula CnH2n+2.

  6. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    As with organic compounds, the cis isomer is generally the more reactive of the two, being the only isomer that can reduce alkenes and alkynes to alkanes, but for a different reason: the trans isomer cannot line its hydrogens up suitably to reduce the alkene, but the cis isomer, being shaped differently, can.

  7. Organoaluminium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoaluminium_chemistry

    Organoaluminium chemistry is the study of compounds containing bonds between carbon and aluminium. It is one of the major themes within organometallic chemistry. [1][2] Illustrative organoaluminium compounds are the dimer trimethylaluminium, the monomer triisobutylaluminium, and the titanium-aluminium compound called Tebbe's reagent.

  8. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    The double bond of an alpha olefin is between the #1 and #2 (IUPAC) or α and β (common) carbon atoms. 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 CxH2x, distinguished by having a double bond at the primary ...

  9. Reductions with diimide - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_diimide

    The transition state of the hydrogen transfer step is likely early; however, high stereoselectivity has been obtained in many reductions of chiral alkenes. [6] (3) The order of reactivity of unsaturated substrates is: alkynes, allenes > terminal or strained alkenes > substituted alkenes. Trans alkenes react more rapidly than cis alkenes in ...