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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. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    Cyclopentadiene Cyclobutene: Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...

  5. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The Sandmeyer reaction can also be used to convert aryl amines to phenols proceeding through the formation of an aryl diazonium salt. In the presence of copper catalyst, such as copper(I) oxide , and an excess of copper(II) nitrate , this reaction takes place readily at room temperature neutral water. [ 28 ]

  6. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Diels–Alder_reaction

    The reaction of cyclopentadiene and butenone for example is 700 times faster in water relative to 2,2,4-trimethylpentane as solvent. [14] Several explanations for this effect have been proposed, such as an increase in effective concentration due to hydrophobic packing [15] or hydrogen-bond stabilization of the transition state. [16]

  7. Category:Cyclopentadienes - Wikipedia

    en.wikipedia.org/wiki/Category:Cyclopentadienes

    This list may not reflect recent changes. ... Trimethylsilyl cyclopentadiene This page was last edited on 4 April 2020, at 10:27 (UTC). Text ...

  8. Today’s NYT ‘Strands’ Hints, Spangram and Answers for ...

    www.aol.com/today-nyt-strands-hints-spangram...

    According to the New York Times, here's exactly how to play Strands: Find theme words to fill the board. Theme words stay highlighted in blue when found.

  9. Pentamethylcyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentamethylcyclopentadiene

    1,2,3,4,5-Pentamethylcyclopentadiene is a cyclic diene with the formula C 5 (CH 3) 5 H, often written C 5 Me 5 H, where Me is CH 3. [3] It is a colorless liquid. [1]1,2,3,4,5-Pentamethylcyclopentadiene is the precursor to the ligand 1,2,3,4,5-pentamethylcyclopentadienyl, which is often denoted Cp* (C 5 Me 5) and read as "C P star", the "star" signifying the five methyl groups radiating from ...