Search
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/23%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/23%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
- https://chem.libretexts.org/Courses/Smith_College/CHM_223_Chemistry_III%3A_Organic_Chemistry_(2024)/07%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/23%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/23%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/09%3A_Carbonyl_Condensation_ReactionsCarbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-...Carbonyl condensation reactions take place between two carbonyl containing reactants, one of which must possess an alpha-hydrogen atom. The first step of the reaction involves the removal of an alpha-hydrogen atom by a base. In the second step, the enolate anion that results from this removal attacks the carbonyl-carbon of the second reacting molecule. In the final step , a proton is transferred to the tetrahedral intermediate formed in the second step, but may subsequently be dehydrated.
