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  2. Primary alcohol - Wikipedia

    en.wikipedia.org/wiki/Primary_alcohol

    A primary alcohol is an alcohol in which the hydroxy group is bonded to a primary carbon atom. It can also be defined as a molecule containing a “–CH 2 OH” group. [ 1 ] In contrast, a secondary alcohol has a formula “–CHROH” and a tertiary alcohol has a formula “–CR 2 OH”, where “R” indicates a carbon-containing group.

  3. Alcohol (chemistry) - Wikipedia

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

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  4. Category:Primary alcohols - Wikipedia

    en.wikipedia.org/wiki/Category:Primary_alcohols

    See primary alcohols for description. Subcategories. This category has the following 3 subcategories, out of 3 total. E. Ethanol (2 C, 18 P) Ethanolamines (4 C, 81 P) H.

  5. Primary alcohols - Wikipedia

    en.wikipedia.org/?title=Primary_alcohols&redirect=no

    From Wikipedia, the free encyclopedia. Redirect page

  6. List of alkanols - Wikipedia

    en.wikipedia.org/wiki/List_of_alkanols

    This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2. Ethanol; C3 1-Propanol ... This page was last edited on 27 March 2024, ...

  7. 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. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  8. Krische allylation - Wikipedia

    en.wikipedia.org/wiki/Krische_allylation

    A remarkable feature of these reactions is the ability to conduct carbonyl allylation from the alcohol oxidation state. Due to a kinetic preference for primary alcohol dehydrogenation, diols containing both primary and secondary alcohols undergo site-selective carbonyl allylation at the primary alcohol without the need for protecting groups. [18]

  9. Fatty alcohol - Wikipedia

    en.wikipedia.org/wiki/Fatty_alcohol

    An example of a fatty alcohol. Fatty alcohols (or long-chain alcohols) are usually high-molecular-weight, straight-chain primary alcohols, but can also range from as few as 4–6 carbons to as many as 22–26, derived from natural fats and oils. The precise chain length varies with the source.