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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The prefix form is "amino-". For secondary amines (of the form R−NH−R), the longest carbon chain attached to the nitrogen atom becomes the primary name of the amine; the other chain is prefixed as an alkyl group with location prefix given as an italic N: CH 3 NHCH 2 CH 3 is N-methylethanamine.

  3. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    While the use of the affix mono-is rarely necessary in organic chemistry, it is often essential in inorganic chemistry to avoid ambiguity: carbon oxide could refer to either carbon monoxide or carbon dioxide. In forming compound affixes, the numeral one is represented by the term hen-except when it forms part of the number eleven (undeca-): hence

  4. Meta (chemistry) - Wikipedia

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

    In organic chemistry, meta indicates the positions of substituents in aromatic cyclic compounds. The substituents have the 1,3-positions, for example in resorcinol. Meta may also denote the dehydrated form of an acid, salt or organic derivative in a series. For example: metabisulfite: 2 bisulfite (HSO − 3) → 1 metabisulfite (S 2 O 2− 5 ...

  5. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    Chemical nomenclature is a set of rules to generate systematic names for chemical compounds.The nomenclature used most frequently worldwide is the one created and developed by the International Union of Pure and Applied Chemistry (IUPAC).

  6. Locant - Wikipedia

    en.wikipedia.org/wiki/Locant

    Organic molecules with more than one functional group can be a source of confusion. Generally the functional group responsible for the name or type of the molecule is the 'reference' group for purposes of carbon-atom naming. For example, the molecules nitrostyrene and phenethylamine are quite similar; the former can even be reduced into the latter.

  7. Alk- - Wikipedia

    en.wikipedia.org/wiki/Alk-

    Prefixes, suffixes, and infixes are known as organic chemistry affixes. These affixes provide details about the molecule's structure, such as the quantity of carbon atoms, the kind of carbon-to-carbon bonds, and the existence of functional groups. [2] The following are a few typical additions in organic chemistry: Prefixes

  8. Wikipedia:Naming conventions (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Wikipedia:Naming...

    Non-numerical prefixes are italicized and uncapitalized in titles (tert-Butyl alcohol, for example). Both numerical and non-numerical prefixes are followed by a hyphen. The template {{DISPLAYTITLE}} is used to display titles which start with lowercase letters or include italics.

  9. Arene substitution pattern - Wikipedia

    en.wikipedia.org/wiki/Arene_substitution_pattern

    Trimethylsilyl, tert-butyl, and isopropyl groups can form stable carbocations, hence are ipso directing groups. Meso-substitution refers to the substituents occupying a benzylic position. It is observed in compounds such as calixarenes and acridines. Peri-substitution occurs in naphthalenes for substituents at the 1 and 8 positions. [citation ...

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