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- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/01%3A_CHEM_1151_Organic_Review/1.S%3A_CHEM_1151_Organic_Review_(Summary)Summary of Chapter.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.15%3A_Substitution_ReactionsThis page discusses halothane, an anesthetic, and its limited use due to toxicity. It explains substitution reactions in organic compounds, detailing how alkyl halides form from methane and chlorine, ...This page discusses halothane, an anesthetic, and its limited use due to toxicity. It explains substitution reactions in organic compounds, detailing how alkyl halides form from methane and chlorine, and further reactions producing dichloromethane and carbon tetrachloride. The text also covers halogen substitution in benzene and the introduction of alkyl groups, as well as the formation of alcohol from alkyl halides through reactions with bases.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introductory_Chemistry_(CK-12)/25%3A_Organic_Chemistry/25.16%3A_Addition_ReactionsThis page compares margarine and butter, noting margarine's cost-effectiveness, lower fat content, and extended shelf life due to hydrogenated vegetable fats. It also covers addition reactions, partic...This page compares margarine and butter, noting margarine's cost-effectiveness, lower fat content, and extended shelf life due to hydrogenated vegetable fats. It also covers addition reactions, particularly hydrogenation, which converts alkenes to alkanes using a platinum catalyst, and hydration reactions involving water and alkenes. Additionally, the text points out that benzene is resistant to addition reactions under mild conditions but can react under high temperatures and pressure.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/01%3A_CHEM_1151_Organic_Review/1.05%3A_Halogenated_AlkanesThe replacement of an hydrogen atom on an alkane by a halogen atom—F, Cl, Br, or I—forms a halogenated compound.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/01%3A_CHEM_1151_Organic_Review/1.E%3A_CHEM_1151_Organic_Review_(Exercises)Select problems and solutions to chapter.
- 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.
