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  2. Menthol - Wikipedia

    en.wikipedia.org/wiki/Menthol

    Chemical formula. C 10 H 20 O: Molar mass: ... Menthol is an organic compound, ... It begins with the synthesis of the terpene limonene, ...

  3. Menthone - Wikipedia

    en.wikipedia.org/wiki/Menthone

    In the experimental laboratory, l-menthone may be prepared by oxidation of menthol with acidified dichromate. [ 10 ] [ needs update ] If the chromic acid oxidation is performed with stoichiometric oxidant in the presence of diethyl ether as co-solvent, a method introduced by H.C. Brown and colleagues in 1971, the epimerization of l -menthone to ...

  4. Monoterpene - Wikipedia

    en.wikipedia.org/wiki/Monoterpene

    [15] [16] Menthol, hinokitiol and thymol are also used in oral hygiene products. Thymol also has antiseptic and disinfectant properties. [17] Volatile monoterpenes produced by plants can attract or repel insects, thus some of them are used in insect repellents, such as citronellol, eucalyptol, limonene, linalool, hinokitiol, menthol and thymol ...

  5. Menthol (data page) - Wikipedia

    en.wikipedia.org/wiki/Menthol_(data_page)

    Phase behavior Triple point? K (? °C), ? Pa Critical point? K (? °C), ? Pa Std enthalpy change of fusion, Δ fus H o? kJ/mol Std entropy change of fusion, Δ fus S oJ/(mol·K)

  6. Alcohol (chemistry) - Wikipedia

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

    The hydroboration-oxidation and oxymercuration-reduction of alkenes are more reliable in organic synthesis. Alkenes react with N-bromosuccinimide and water in halohydrin formation reaction. Amines can be converted to diazonium salts, which are then hydrolyzed.

  7. p-Menthane-3,8-diol - Wikipedia

    en.wikipedia.org/wiki/P-Menthane-3,8-diol

    p-Menthane-3,8-diol, also known as para-menthane-3,8-diol, PMD, or menthoglycol, is an organic compound classified as a diol and a terpenoid.It is colorless. Its name reflects the hydrocarbon backbone, which is that of p-menthane.

  8. Benzilic acid rearrangement - Wikipedia

    en.wikipedia.org/wiki/Benzilic_acid_rearrangement

    It has become a classic reaction in organic synthesis and has been reviewed many times before. [3] [4] [5] It can be viewed as an intramolecular redox reaction, as one carbon center is oxidized while the other is reduced. Scheme 1. Benzilic acid rearrangement

  9. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters.The reaction mainly applies to primary and secondary alcohols.