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  2. 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.

  3. Prilezhaev reaction - Wikipedia

    en.wikipedia.org/wiki/Prilezhaev_reaction

    An illustrative example is the epoxidation of trans-2-butene with m-CPBA to give trans-2,3-epoxybutane: [4] The oxygen atom that adds across the double bond of the alkene is taken from the peroxy acid, generating a molecule of the corresponding carboxylic acid as a byproduct.

  4. 2-Pentyne - Wikipedia

    en.wikipedia.org/wiki/2-Pentyne

    Ethylmethylacetylene, 1-Ethyl-2-methylacetylene propyl acetylene. ... 2-Pentyne, an organic compound with the formula CH 3 CH 2 C≡CCH 3 and is an internal alkyne.

  5. Reductive elimination - Wikipedia

    en.wikipedia.org/wiki/Reductive_elimination

    The rate of reductive elimination is greatly influenced by the geometry of the metal complex. In octahedral complexes, reductive elimination can be very slow from the coordinatively saturated center; and often, reductive elimination only proceeds via a dissociative mechanism, where a ligand must initially dissociate to make a five-coordinate ...

  6. Oxymercuration reaction - Wikipedia

    en.wikipedia.org/wiki/Oxymercuration_reaction

    In organic chemistry, the oxymercuration reaction is an electrophilic addition reaction that transforms an alkene (R 2 C=CR 2) into a neutral alcohol. In oxymercuration, the alkene reacts with mercuric acetate (AcO−Hg−OAc) in aqueous solution to yield the addition of an acetoxymercury (−HgOAc) group and a hydroxy (−OH) group across the ...

  7. Electrocyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Electrocyclic_reaction

    The increased reaction rate for the trimethylsilyl compound can be explained by silicon hyperconjugation as the βC-Si bond weakens the cyclobutane C-C bond by donating electrons. Scheme 2. benzocyclobutane ring opening. A biomimetic electrocyclic cascade reaction was discovered in relation to the isolation and synthesis of certain endiandric ...

  8. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Because the cis–trans and E–Z systems compare different groups on the alkene, it is not strictly true that Z corresponds to cis and E corresponds to trans. For example, trans-2-chlorobut-2-ene (the two methyl groups, C1 and C4, on the but-2-ene backbone are trans to each other) is (Z)-2-chlorobut-2-ene (the chlorine and C4 are together ...

  9. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For monoalkenes, the configuration is often indicated by the prefixes cis- (from Latin "on this side of") or trans- ("across", "on the other side of") before the name, respectively; as in cis-2-pentene or trans-2-butene. The difference between cis-and trans-isomers