Propose mechanisms and products for the following transformations. Use the curved-arrow formalism to depict electron movement and show all intermediates/charges. a) b) c) d) НО. CF3 OH NO₂ F₂C Et N CH₂Cl₂, 0 °C CH3 N-CH3 CF3 toluene, 100 °C NH₂ 2) CH₂ CH₂CN, 45 °C 1) SOCI₂, Et₂N NH E CH₂ CH₂
Propose mechanisms and products for the following transformations. Use the curved-arrow formalism to depict electron movement and show all intermediates/charges. a) b) c) d) НО. CF3 OH NO₂ F₂C Et N CH₂Cl₂, 0 °C CH3 N-CH3 CF3 toluene, 100 °C NH₂ 2) CH₂ CH₂CN, 45 °C 1) SOCI₂, Et₂N NH E CH₂ CH₂
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...
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