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  2. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Identification of the side-chains. Side chains are the carbon chains that are not in the parent chain, but are branched off from it. Identification of the remaining functional groups, if any, and naming them by their ionic prefixes (such as hydroxy for −OH, oxy for =O, oxyalkane for O−R, etc.).

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  4. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl. Ethanol is a volatile, flammable, colorless liquid with a characteristic wine-like ...

  5. Alcohol (chemistry) - Wikipedia

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

    The red and white balls represent the hydroxyl group (−OH). The three "R"s stand for carbon substituents or hydrogen atoms. [1] In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom.

  6. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    This is a free rotation only in the simplest cases like gaseous methyl chloride CH 3 Cl. In most molecules, the remainder R breaks the C ∞ symmetry of the R−C axis and creates a potential V(φ) that restricts the free motion of the three protons. For the model case of ethane CH 3 CH 3, this is discussed under the name ethane barrier. In ...

  7. Carbocation - Wikipedia

    en.wikipedia.org/wiki/Carbocation

    The tert-butyl cation is a relatively stable carbenium ion. [1] A carbocation is an ion with a positively charged carbon atom. Among the simplest examples are the methenium CH + 3, methanium CH + 5, acylium ions RCO +, and vinyl C 2 H + 3 cations. [2] Until the early 1970s, carbocations were called carbonium ions. [3]

  8. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids (R−C(=O)OH). A specific example of an acyl chloride is acetyl chloride, CH 3 COCl.

  9. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    Experiments and calculations generally agree that the methenium ion is planar, with threefold symmetry. [3] The carbon atom is a prototypical (and exact) example of sp 2 hybridization. Preparation and reactions