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Carboxylic Acid Preparation


Fischer Esterification


Methyl Ester Preparation


Acid Chloride Formation


Nucleophilic Acyl Addition


Acid Chloride Hydrolysis


Dicarbonyl Hydrolysis


Ester Hydrolysis


Amide Hydolysis


Nitrile Hydrolysis


Acid Chloride + Alcohol


Dicarbonyl + Alcohol


Ester + Alcohol


Acid Chloride + Amine


Dicarbonyl + Amine


Ester + Amine


Acid Chloride + Carboxylic Salt


Ester + Gringard


Ester + Organolithium


Acid Chloride + Gilman


Ester Reduction


Ester Reduction


Amide Reduction


Nitrile Reduction


Enolate Anion Formation


Enolate Anion Alkylation


Carbonyl Addition


Aldol Reaction


Acid Catalyzed Dehydration


Claisen Condensation


Diekmann Condensation


Decarboxilation


Enamine Formation


Alkylation of Enamines


Acylation of Enamines


Acetoacetic Substitution


Acetoacetic Saponification


Acetoacetic Decarboxilation


Michael Addition


Robinson Annulation


Conjugate Addition of Lithium Diorgano-Copper


Crossed Enolate Reaction


Grignard Formation


Organolithium Formation










Gillman Preparation




Carbene Prep




Simmons-Smith Synthesis






Wittig Rxn


Wittig Prep 1


Wittig Prep 2


HWE Rxn 1


HWE Rxn 2
“E”!!!


Hemiacetals


Acetals


Primary Amine
Imine


Secondary Amine
Enamine


Keto-Enol Tautomers


Keto-Enol Equilibrium


Deuterium Exchange






Pinnick Oxidation


NaBH4 cannot reduce carboxylic acids to primary alcohols, only LAH








Clemmensen


Wolff-Kischner
















Anti-Markovnikov




Simmons-Smith Rxn (Can write CH2I2 and Zn(Cu) as reactants)
cyclopropane formation


Diels Alder Reaction


Cyclohexene Reduction


Benzene Reduction


Williamson Ether Synthesis


Benzylic Oxidation


Benzylic Halogenation


Hydrogenolysis


Benzene Chlorination


Benzene Bromination


Nitrobenzene Amination


Nitrobenzene Amination


Sulfonation


Friedel-Crafts Alkylation


Friedel-Crafts Acylation
