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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Nomenclature_Workbook_(O'Donnell)/01%3A_Chapters/1.01%3A_Unbranched_AlkanesThe page discusses the naming of unbranched alkanes, which are saturated hydrocarbons with only single carbon-carbon bonds and maximum hydrogen atoms. It provides a table listing alkanes with up to te...The page discusses the naming of unbranched alkanes, which are saturated hydrocarbons with only single carbon-carbon bonds and maximum hydrogen atoms. It provides a table listing alkanes with up to ten carbon atoms, including methane, ethane, propane, and others, with their molecular and condensed structural formulas, and boiling points.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Nomenclature_Workbook_(O'Donnell)/01%3A_Chapters/1.03%3A_Alkyl_SubstituentsThis page provides guidance on naming organic molecules with alkyl substituents. An alkyl group is an alkane-derived substituent attached to a molecular structure to form a branched molecule. Alkyl gr...This page provides guidance on naming organic molecules with alkyl substituents. An alkyl group is an alkane-derived substituent attached to a molecular structure to form a branched molecule. Alkyl groups are named similarly to straight-chain alkanes. Several examples, such as methyl, ethyl, propyl, and butyl groups, are given, with condensed structures listed. The page further explains the IUPAC naming system, using a prefix, parent, and suffix.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Nomenclature_Workbook_(O'Donnell)/01%3A_Chapters/1.06%3A_Benzene_and_ConjugationThe page provides an educational overview of naming benzene derivatives, explaining the unique chemistry and unexpected stability of aromatic hydrocarbons. Despite being labeled as 1,3,5-cyclohexatrie...The page provides an educational overview of naming benzene derivatives, explaining the unique chemistry and unexpected stability of aromatic hydrocarbons. Despite being labeled as 1,3,5-cyclohexatriene, benzene's double bonds do not behave as typical alkenes due to electron sharing, forming a conjugated system. The text explains naming conventions for benzene derivatives, including positional terms like ortho, meta, and para.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Nomenclature_Workbook_(O'Donnell)/01%3A_Chapters/1.05%3A_HalogensThis page provides a guide to naming halogenated hydrocarbons, emphasizing the use of halogens from Group 7A, including fluorine, chlorine, bromine, and iodine, in reactions to form alkyl halides. It ...This page provides a guide to naming halogenated hydrocarbons, emphasizing the use of halogens from Group 7A, including fluorine, chlorine, bromine, and iodine, in reactions to form alkyl halides. It explains the IUPAC system of nomenclature using the prefix-parent-suffix method to reflect the molecule's substituents, carbon count, and family. Practice questions are posed to apply this knowledge, alongside tasks to write naming instructions and practice naming drawn alkyl halides.
