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  2. Pinacolyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Pinacolyl_alcohol

    3,3-Dimethyl-2-butanol. ... Pinacolyl alcohol (also known as 3,3-dimethylbutan-2-ol and as pine alcohol) is one of the isomeric hexanols and a secondary alcohol.

  3. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.

  4. Parikh–Doering oxidation - Wikipedia

    en.wikipedia.org/wiki/Parikh–Doering_oxidation

    The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively. [1] The procedure uses dimethyl sulfoxide (DMSO) as the oxidant and the solvent, activated by the sulfur trioxide pyridine complex (SO 3 •C 5 H 5 N) in the presence of triethylamine or diisopropylethylamine as base.

  5. Dimethylbutanol - Wikipedia

    en.wikipedia.org/wiki/Dimethylbutanol

    3,3-Dimethyl-1-butanol (DMB) See also. Dimethylbutane; Hexanol This page was last edited on 1 April 2021, at 21:29 (UTC). Text is available under the Creative ...

  6. Oxonium ion - Wikipedia

    en.wikipedia.org/wiki/Oxonium_ion

    Extreme acidity, heat, and dehydrating conditions are usually required. Other hydrocarbon oxonium ions are formed by protonation or alkylation of alcohols or ethers (R−C− + −R 1 R 2). Secondary oxonium ions have the formula R 2 OH +, an example being protonated ethers. Tertiary oxonium ions have the formula R 3 O +, an example being ...

  7. Pinacol coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Pinacol_coupling_reaction

    The reaction is named after pinacol (also known as 2,3-dimethyl-2,3-butanediol or tetramethylethylene glycol), which is the product of this reaction when done with acetone as reagent. The reaction is usually a homocoupling but intramolecular cross-coupling reactions are also possible. Pinacol was discovered by Wilhelm Rudolph Fittig in 1859

  8. 3-Methyl-2-butanol - Wikipedia

    en.wikipedia.org/wiki/3-Methyl-2-butanol

    3-Methyl-2-butanol (IUPAC name, commonly called sec-isoamyl alcohol) is an organic chemical compound. It is used as a solvent and an intermediate in the manufacture of other chemicals. [ 3 ]

  9. tert-Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_alcohol

    tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic [ 3 ] and more recently as a recreational drug . [ 4 ] TAA is mostly a positive allosteric modulator for GABA A receptors in the same way as ethanol . [ 5 ]