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  • https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_Nomenclature_Workbook_(O'Donnell)/01%3A_Chapters/1.01%3A_Unbranched_Alkanes
    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 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/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.02%3A_Straight-Chain_Alkanes
    This page explores the viability of propane gas as an alternative transportation fuel, highlighting its efficiency, power, and lower pollution compared to gasoline. It also defines hydrocarbons, class...This page explores the viability of propane gas as an alternative transportation fuel, highlighting its efficiency, power, and lower pollution compared to gasoline. It also defines hydrocarbons, classifying them into aliphatic and aromatic types, with a focus on alkanes, which consist solely of single covalent bonds. The text outlines naming conventions for straight-chain alkanes and provides a table of the first ten alkanes in the series.
  • https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.03%3A_Branched_Alkanes
    This page discusses the identification of family trees and the naming of branched alkanes. It emphasizes the importance of precise relative naming for family trees and explains structural isomers, hig...This page discusses the identification of family trees and the naming of branched alkanes. It emphasizes the importance of precise relative naming for family trees and explains structural isomers, highlighting that they share the same molecular formula but differ in structure.
  • https://chem.libretexts.org/Bookshelves/General_Chemistry/Book%3A_Structure_and_Reactivity_in_Organic_Biological_and_Inorganic_Chemistry_(Schaller)/I%3A__Chemical_Structure_and_Properties/06%3A_Conformational_Analysis/6.03%3A_Conformation_of_Butane
    At 60 degrees, the molecule is no longer eclipsed, and just as in ethane the energy is a little bit lower, but the overall shape when viewed from the side is still a sort of twisted C. This factor is ...At 60 degrees, the molecule is no longer eclipsed, and just as in ethane the energy is a little bit lower, but the overall shape when viewed from the side is still a sort of twisted C. This factor is called "sterics" and it refers to the idea that molecules, or parts of molecules, take up space, and so two parts of the butane can't occupy the same place at the same time.

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