有机化学暑期课程教学大纲
【课程名称COURSE TITLE】） 有机化学
【授课教师INSTRUCTOR】
姓 名：Yi Pang
国 籍：美国 职 称：教授
来自学校：The University of Akron Email地址：
【授课对象STUDENTS】
本科生
【授课语言TEACHING LANGUAGE】
英语
【授课方式METHODS OF INSTRUCTION】
课堂讲授为主，学生分组讨论
【课堂规模CLASSROOM CAPACITY】
20-40人
【课程考核EVALUATION】
出勤考核、课堂参与、随堂测验
【课程学分CREDITS】
1 学分 （16学时）
【课程教材Textbooks】
Organic Chemistry（8e），John McMurry，2012
【课程简介COURSE DESCRIPTION】
Organic chemistry is a fundamental academic course. This course is opened for those major in chemistry biology and relative specialty. It mainly introduce the basic organic theory, such as the structure , property and synthesis of organic compound. It give background knowledge for the future courses such as biochemistry.
【课程内容及教学进度SYLLABUS】
1. Structure and Bonding（3h）
1.1 Atomic Structure: The Nucleus 1.2 Atomic Structure: Orbitals
1.3 Atomic Structure: Electron Configurations 1.4 Development of Chemical Bonding Theory
1.5 Describing Chemical Bonds: Valence Bond Theory 1.6 sp 3 Hybrid Orbitals and the Structure of Methane 1.7 sp 3 Hybrid Orbitals and the Structure of Ethane 1.8 sp 2 Hybrid Orbitals and the Structure of Ethylene 1.9 sp Hybrid Orbitals and the Structure of Acetylene
1.10 Hybridization of Nitrogen, Oxygen, Phosphorus, and Sulfur 1.11 Describing Chemical Bonds: Molecular Orbital Theory
2. Polar Covalent Bonds; Acids and Bases（3h）
2.1 Polar Covalent Bonds: Electronegativity 2.2 Polar Covalent Bonds: Dipole Moments 2.3 Formal Charges 2.4 Resonance
2.5 Rules for Resonance Forms
2.6 Drawing Resonance Forms
2.7 Acids and Bases: The Br?nsted–Lowry Definition 2.8 Acid and Base Strength
2.9 Predicting Acid–Base Reactions from pK a Values 2.10 Organic Acids and Organic Bases 2.11 Acids and Bases: The Lewis Definition
2.12 Noncovalent Interactions Between Molecules
3.1 Enantiomers and the Tetrahedral Carbon
3.2 The Reason for Handedness in Molecules: Chirality 3.3 Optical Activity
3.4 Pasteur’s Discovery of Enantiomers
3.5 Sequence Rules for Specifying Configuration 3.6 Diastereomers 3.7 Meso Compounds
3.8 Racemic Mixtures and the Resolution of Enantiomers 3.9 A Review of Isomerism
3. Stereochemistry at Tetrahedral Centers（3h）
3.10 Chirality at Nitrogen, Phosphorus, and Sulfur 3.11 Prochirality
4. An Overview of Organic Reactions （3h）
4.1 Kinds of Organic Reactions
4.2 How Organic Reactions Occur: Mechanisms 4.3 Radical Reactions 4.4 Polar Reactions
4.5 An Example of a Polar Reaction: Addition of HBr to Ethylene 4.6 Using Curved Arrows in Polar Reaction Mechanisms
4.7 Describing a Reaction: Equilibria, Rates, and Energy Changes 4.8 Describing a Reaction: Bond Dissociation Energies
4.9 Describing a Reaction: Energy Diagrams and Transition States 4.10 Describing a Reaction: Intermediates
5. pericyclic reactions（4h）
5.1 Molecular Orbitals of Conjugated Pi Systems 5.2 Electrocyclic Reactions
5.3 Stereochemistry of Thermal Electrocyclic Reactions 5.4 Photochemical Electrocyclic Reactions
5.5 Cycloaddition Reactions
5.6 Stereochemistry of Cycloadditions 5.7 Sigmatropic Rearrangements
5.8 Some Examples of Sigmatropic Rearrangements 5.9 A Summary of Rules for Pericyclic Reactions
化学与药学院 2019年4月25日
有机化学暑期课程教学大纲 - 图文
