Search
- https://chem.libretexts.org/Courses/Honolulu_Community_College/CHEM_100%3A_Chemistry_and_Society/10%3A_Organic_Chemistry/10.03%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/University_of_Kansas/General%2C_Organic%2C_and_Biological_Chemistry/11%3A_Organic_Chemistry/11.02%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/University_of_Kansas/CHEM_110%3A_Introductory_Chemistry_(Sharpe_Elles)_SP25/11%3A_Organic_Chemistry/11.02%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.07%3A_Aromatic_HydrocarbonsThis page discusses Friedrich Kekulé, a 19th-century chemist who conceptualized benzene's cyclic structure, inspired by a dream. Benzene, an aromatic hydrocarbon with six hydrogen atoms and stabilizin...This page discusses Friedrich Kekulé, a 19th-century chemist who conceptualized benzene's cyclic structure, inspired by a dream. Benzene, an aromatic hydrocarbon with six hydrogen atoms and stabilizing delocalized pi electrons, has varied nomenclature based on its substituents. Basic naming involves alkyl groups, while arrangements with multiple substituents are identified by position numbers or ortho, meta, and para prefixes.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.03%3A_Branched_AlkanesThis 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/Courses/Portland_Community_College/CH100%3A_Everyday_Chemistry/08%3A_Energy_from_Fossil_Fules/8.05%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/Nassau_Community_College/Principles_of_Chemistry/16%3A_Organic_Chemistry/16.03%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Beginning_Chemistry_(Ball)/16%3A_Organic_Chemistry/16.03%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/Fullerton_College/Beginning_Chemistry_(Chan)/17%3A_Organic_Chemistry/17.03%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- 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.
