Orgo 2: Unit 5 Reactions
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162 Terms
Acid Chloride
Ester
Anhydride
Amide
General Reaction for Nucleophilic Substitution Mechanism (4 types)
Nucleophilic Acyl Substitution Mechanism
Carboxylate salt
Ammonium salt
(any combo of H and R groups, just has to be 4 to make quaternary + charge on salt aka N)
Acid Chloride Hydrolysis General Reaction
Acid Chloride Hydrolysis Mechanism (CAD Nucleophilic Acyl Substitution)
Acid Chloride Alcoholysis General Reaction
Acid Chloride Alcoholysis Mechanism CAD
General Reaction
Acid Chloride Aminolysis CAD Mechanism
Anhydride to Ester General Reaction
Anhydride to Ester General Mechanism Utilizing Alcohols
Transesterification General Reaction
Transesterification General Reaction Example
Base Catalyzed Transesterification Mechanism
Acid Catalyzed Transesterification Mechanism
Saponification General Reaction
Saponification Mechanism
General Reaction of Amide Hydrolysis
Acidic Hydrolysis of Amines Mechanism
General Reaction of Basic Hydrolysis of Amides
Mechanism of Basic Hydrolysis of Amides
Making an Acid Chloride General Reaction
Making an Acid Chloride Mechanism
Ester to Aldehyde General Reaction
Ester to Alcohol General Reaction
Reducing an Ester to Aldehyde Reaction
Reducing an Acid Chloride to Aldeyde General Reaction
Reducing an Acid Chloride to Aldehyde Part II
Ester to Alehyde using Li
Nitrile
General Reaction: SN2 of Nitriles
Creating Nitriles via SN2 Mechanism
Dehydration of Amides—>Nitriles General Reaction
Dehydration of Amides—>Nitriles Mechanism
Acidic Nitrile Hydrolysis General Reaction
Acidic Nitrile Hydrolysis Mechanism
