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- https://chem.libretexts.org/Courses/Alma_College/Organic_Chemistry_I_(Alma_College)/09%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/9.08%3A_Elimination_Reactions-_Zaitsev's_RuleIn the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breakin...In the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic carbon, and the formation of a pi bond between these two carbons.
- https://chem.libretexts.org/Courses/Nassau_Community_College/Organic_Chemistry_I_and_II/06%3A_Alkyl_Halides%3A_Nucleophilic_Substitution_and_Elimination/6.14%3A_Zaitsev's_RuleZaitsev's Rule can be used to predict the regiochemistry of elimination reactions. Regiochemistry describes the orientation of reactions about carbon-carbon double bonds (C=C).
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/11%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.08%3A_Elimination_Reactions-_Zaitsev's_RuleIn the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breakin...In the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic carbon, and the formation of a pi bond between these two carbons.
- https://chem.libretexts.org/Courses/Sacramento_City_College/SCC%3A_Chem_420_-_Organic_Chemistry_I/Text/07%3A_Alkyl_Halides%3A_Nucleophilic_Substitution_and_Elimination/7.14%3A_Zaitsev's_RuleZaitsev's Rule can be used to predict the regiochemistry of elimination reactions. Regiochemistry describes the orientation of reactions about carbon-carbon double bonds (C=C).
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/11%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.08%3A_Elimination_Reactions-_Zaitsev's_RuleAccording to Zaitsev’s rule, formulated in 1875 by the Russian chemist Alexander Zaitsev, base-induced elimination reactions generally (although not always) give the more stable alkene product—that is...According to Zaitsev’s rule, formulated in 1875 by the Russian chemist Alexander Zaitsev, base-induced elimination reactions generally (although not always) give the more stable alkene product—that is, the alkene with more alkyl substituents on the double-bond carbons. To find the products in a specific case, locate the hydrogen atoms on each carbon next to the leaving group, and then generate the potential alkene products by removing HX in as many ways as possible.
- https://chem.libretexts.org/Courses/Smith_College/CHM_223_Chemistry_III%3A_Organic_Chemistry_(2024)/02%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/2.08%3A_Elimination_Reactions-_Zaitsev's_RuleFor most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic c...For most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic carbon, and the formation of a pi bond between these two carbons.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/11%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.07%3A_Elimination_Reactions-_Zaitsev's_RuleIn the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breakin...In the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic carbon, and the formation of a pi bond between these two carbons.
- https://chem.libretexts.org/Courses/Chabot_College/Chem_12A%3A_Organic_Chemistry_Fall_2022/09%3A_Elimination_Reactions/9.03%3A_Zaitsev's_RuleZaitsev's Rule can be used to predict the regiochemistry of elimination reactions. Regiochemistry describes the orientation of reactions about carbon-carbon double bonds (C=C).
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/11%3A_Reactions_of_Alkyl_Halides-_Nucleophilic_Substitutions_and_Eliminations/11.07%3A_Elimination_Reactions-_Zaitsev's_RuleIn the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breakin...In the second step of the mechanism the lone pair electrons of the carbanion move to become the pi bond of the alkene. For most elimination reactions, the formation of the product involves the breaking of a C-X bond from the electrophilic carbon, the breaking of a C-H bond from a carbon adjacent to the electrophilic carbon, and the formation of a pi bond between these two carbons.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Alkenes/Synthesis_of_Alkenes/Zaitsev's_RuleZaitsev's Rule can be used to predict the regiochemistry of elimination reactions.
- https://chem.libretexts.org/Workbench/Chemistry_LHS_Bridge/13%3A_Alkenes/13.03%3A_Synthesis_of_Alkenes/13.3.08%3A_Zaitsev's_RuleZaitsev's Rule can be used to predict the regiochemistry of elimination reactions.
