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  2. IUPAC nomenclature of organic chemistry - Wikipedia

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

    In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended [1] [2] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). [3]

  3. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Combining the names of functional groups with the names of the parent alkanes generates what is termed a systematic nomenclature for naming organic compounds. In traditional nomenclature, the first carbon atom after the carbon that attaches to the functional group is called the alpha carbon ; the second, beta carbon, the third, gamma carbon, etc.

  4. -ane - Wikipedia

    en.wikipedia.org/wiki/-ane

    In organic chemistry, the suffix-ane forms the names of organic compounds where the −C−C− group (a carbon-carbon single bond) has been attributed the highest priority according to the rules of organic nomenclature. Such organic compounds are called alkanes. They are saturated hydrocarbons.

  5. Preferred IUPAC name - Wikipedia

    en.wikipedia.org/wiki/Preferred_IUPAC_name

    The concept of PINs is defined in the introductory chapter and chapter 5 of the "Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013" (freely accessible), [4] which replace two former publications: the "Nomenclature of Organic Chemistry", 1979 (the Blue Book) and "A Guide to IUPAC Nomenclature of Organic Compounds ...

  6. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H 14: n-hexane

  7. Alk- - Wikipedia

    en.wikipedia.org/wiki/Alk-

    The root alk-is used in organic chemistry to form classification names for classes of organic compounds which contain a carbon skeleton but no aromatic rings. It was extracted from the word alcohol by removing the -ol suffix. See e.g. alkyl, alkane. [1

  8. -ol - Wikipedia

    en.wikipedia.org/wiki/-ol

    The IUPAC name of alcohols can derive from the following rules: Identify the longest carbon chain, and number each carbon. Name the base alkane according to the organic nomenclature rules. Identify the hydroxyl group and which carbon it is on. To be alcohol, the -OH must be bonded to a carbon.

  9. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula C n H 2n+2.

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