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  2. Cyclopentanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopentanol

    Cyclopentanol or cyclopentyl alcohol is a cyclic alcohol. It is also known as hydroxycyclopentane. ... Reactions. The dehydration of cyclopentanol produces ...

  3. Cyclopentene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentene

    In the laboratory, it is prepared by dehydration of cyclopentanol. [4] Substituted cyclopentenes are the product of the vinylcyclopropane-cyclopentene rearrangement. [5] It can also be produced by the catalytic hydrogenation of cyclopentadiene. [6]

  4. 3-Methyl-3-pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Methyl-3-pentanol

    This article about an alcohol is a stub. You can help Wikipedia by expanding it.

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    Tertiary alcohols react with strong acids to generate carbocations. The reaction is related to their dehydration, e.g. isobutylene from tert-butyl alcohol. A special kind of dehydration reaction involves triphenylmethanol and especially its amine-substituted derivatives. When treated with acid, these alcohols lose water to give stable ...

  6. 3-Pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Pentanol

    This article about an alcohol is a stub. You can help Wikipedia by expanding it.

  7. 2-Methyl-2-pentanol - Wikipedia

    en.wikipedia.org/wiki/2-Methyl-2-pentanol

    2-Methyl-2-pentanol (IUPAC name: 2-methylpentan-2-ol) is an organic chemical compound.It can be added to a gas chromatograph to help distinguish between branched compounds, especially alcohols. [2]

  8. Category:Cyclopentanols - Wikipedia

    en.wikipedia.org/wiki/Category:Cyclopentanols

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  9. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    The Bogert–Cook synthesis (1933) involves the dehydration and isomerization of 1-β-phenylethylcyclohexanol to the octahydro derivative of phenanthrene [23] The Darzens–Nenitzescu synthesis of ketones (1910, 1936) involves the acylation of cyclohexene with acetyl chloride to methylcyclohexenylketone.