Organic Chemistry 3

In-depth study of the aromatic hydrocarbons (benzene substituents) and the carbonyl group, chemistry of amines and their derivatives, chemistry of the heterocycles. Organic chemistry of biologically important molecules: carboxylic acids, carbohydrates, amino acids, peptides, proteins, natural products
Chapters
Concepts
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Exams
The Carbonyls are studied in this chapter: the deoxygenation of carbonyls, the addition of cyanide, the Wittig reaction, the Baeyer-Villiger oxidation. This chapter is a continuation of chapter 7 – Organic Chemistry 2.
Deoxygenation of the Carbonyl Group Addition of Hydrogen Cyanide Wittig Reaction Baeyer-Villiger Oxidation
The Enols and Enolates are studied in this chapter: the halogenation of aldehydes and ketones, the 1,2- and 1,4-additions of organometallic reagents, the Michael addition, the Robinson annulation. This chapter is a continuation of chapter 8 – Organic Chemistry 2.
Halogenation of Aldehydes and Ketones 1,2- and 1,4-Additions of Organometallic Reagents Michael Addition Robinson Annulation
The Carboxylic Acid Derivatives are studied in this chapter: the Hofmann rearrangement, the naming and properties of alkanenitriles, the hydrolysis of nitriles, their reaction with organometallic reagents, their reduction of nitriles. This chapter is a continuation of chapter 10 – Organic Chemistry 2.
Hofmann Rearrangement Alkanenitriles: Naming and Properties Hydrolysis of Nitriles Nitriles and Organometallic reagents Reduction of Nitriles
The Amines and their Derivatives are studied in this chapter: the naming and properties of amines, their synthesis, the Hofmann elimination, the Mannich reaction.
Naming the Amines Properties of Amines Preparation of Amines Hofmann Elimination Mannich Reaction
The Chemistry of Benzene Substituents is studied in this chapter: the reactivity of methylbenzene, the benzylic oxidation and reduction, the nucleophilic aromatic substitution, the properties and reactivities of phenol, the Claisen rearrangement, the arenediazonium salts.
Reactivity of the Methylbenzene Benzylic Oxidation and Reduction Nucleophilic Aromatic Substitution Properties and Reactivities of Phenol Claisen Rearrangement Arenediazonium Salts
The Ester Enolates and the Claisen Condensation are studied in this chapter: the acidity and formation of β-dicarbonyl compounds, the nucleophilicity of β-dicarbonyl anions, the 3-ketoacids decarboxylation, the malonic ester synthesis, the Michael addition.
Acidity of the β-Dicarbonyls Formation of β-Dicarbonyl compounds Other Methods to form β-Dicarbonyl Compounds Nucleophilicity of β-Dicarbonyl Anions 3-Ketoacids Decarboxylation Malonic Ester Synthesis Michael Addition
The Carbohydrates are studied in this chapter: the naming and structures of carbohydrates, the Fischer projection, the conformations and cyclic forms of sugars, the Haworth projection, the oxidation and reduction of sugars, the ester and ether formations, the polysaccharides.
Names and Structures of Carbohydrates Fischer Projection Conformations and Cyclic forms of Sugars Haworth Projection Oxidation of Sugars Reduction of Sugars Ester and Ether Formation Polysaccharides
The Heterocycles are studied in this chapter: the reactivity of nonaromatic heterocycles, the synthesis, properties and reactivity of aromatic heterocyclopentadienes, the synthesis, properties and reactivity of pyridine.
Naming the Heterocycles Reactivity of Nonaromatic Heterocycles Aromatic Heterocyclopentadienes Aromatic Heterocyclopentadienes - Reactivity Pyridine Reactivity of Pyridine
The Amino Acids, Peptides and Proteins are studied in this chapter : the structure and properties of amino acids, the synthesis of amino acids (Hell-Volhard-Zelinsky , Gabriel and Strecker synthesis), the structure and properties of peptides and proteins, the amino acids sequencing, the synthesis of polypeptides, the Merrifield solid-phase peptide synthesis.
Structure and Properties of Amino Acids Synthesis of Amino Acids Peptides and Proteins Amino Acids Sequencing Synthesis of Polypeptides Merrifield Solid-Phase Peptide Synthesis
Midterm 1 includes 5 questions and it covers Organic Chemistry 1, Organic Chemistry 2 and Chapters 1, 2 and 3 of Organic Chemistry 3. At the end of the test you can see the answers and determine whether you have solved the questions. You have 1 hour to resolve Midterm 1.
Questions
60 Minutes
Midterm 2 includes 5 questions and it covers Organic Chemistry 1, Organic Chemistry 2 and chapters 1 to 6 of Organic Chemistry 3 (mainly chapters 4, 5 and 6). At the end of the test you can see the answers and determine whether you have solved the questions. You have 1 hour to resolve Midterm 2.
Questions
60 Minutes
Final Exam includes 13 questions and it covers all chapters of Organic Chemistry 1, 2 and 3. At the end of the test you can see the answers and determine whether you have solved the questions. You have 3 hours to resolve Final Exam.
Questions
180 Minutes