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  2. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    The process, which is catalyzed by platinum supported by aluminium oxide, is exemplified in the conversion methylcyclohexane (a naphthene) into toluene (an aromatic). [2] Dehydrocyclization converts paraffins (acyclic hydrocarbons) into aromatics. [3] A related aromatization process includes dehydroisomerization of methylcyclopentane to benzene:

  3. Cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadiene

    Cyclopentadiene is a highly reactive diene in the Diels–Alder reaction because minimal distortion of the diene is required to achieve the envelope geometry of the transition state compared to other dienes. [11] Famously, cyclopentadiene dimerizes. The conversion occurs in hours at room temperature, but the monomer can be stored for days at ...

  4. Cyclopentadienyliron dicarbonyl dimer - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadienyliron_di...

    Cp 2 Fe 2 (CO) 4 was first prepared in 1955 at Harvard by Geoffrey Wilkinson using the same method employed today: the reaction of iron pentacarbonyl and dicyclopentadiene. [7] [8] 2 Fe(CO) 5 + C 10 H 12 → (η 5-C 5 H 5) 2 Fe 2 (CO) 4 + 6 CO + H 2. In this preparation, dicyclopentadiene cracks to give cyclopentadiene, which reacts with Fe(CO ...

  5. Alkyne trimerisation - Wikipedia

    en.wikipedia.org/wiki/Alkyne_trimerisation

    An alkyne trimerisation is a [2+2+2] cycloaddition reaction in which three alkyne units (C≡C) react to form a benzene ring. The reaction requires a metal catalyst. The process is of historic interest as well as being applicable to organic synthesis. [1] Being a cycloaddition reaction, it has high atom economy.

  6. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The Sandmeyer reaction provides a method through which one can perform unique transformations on benzene, such as halogenation, cyanation, trifluoromethylation, and hydroxylation. The reaction was discovered in 1884 by Swiss chemist Traugott Sandmeyer , when he attempted to synthesize phenylacetylene from benzenediazonium chloride and copper(I ...

  7. Hückel's rule - Wikipedia

    en.wikipedia.org/wiki/Hückel's_rule

    Benzene, the most widely recognized aromatic compound with six delocalized π-electrons (4n + 2, for n = 1). In organic chemistry , Hückel's rule predicts that a planar ring molecule will have aromatic properties if it has 4 n + 2 π-electrons , where n is a non-negative integer .

  8. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Cyclopentene is a chemical compound with the formula (CH 2) 3 (CH) 2. It is a colorless liquid with a petrol-like odor. It has few applications, and thus is mainly used as a minor component of gasoline, present in concentrations of less than 1%. [1] [2] It is one of the principal cycloalkenes.

  9. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...