CHEM C220: Organic Chemistry A
Item | Value |
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Curriculum Committee Approval Date | 10/17/2008 |
Top Code | 190500 - Chemistry, General |
Units | 3 Total Units |
Hours | 54 Total Hours (Lecture Hours 54) |
Total Outside of Class Hours | 0 |
Course Credit Status | Credit: Degree Applicable (D) |
Material Fee | No |
Basic Skills | Not Basic Skills (N) |
Repeatable | No |
Grading Policy | Standard Letter (S) |
Local General Education (GE) |
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California General Education Transfer Curriculum (Cal-GETC) |
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Intersegmental General Education Transfer Curriculum (IGETC) |
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California State University General Education Breadth (CSU GE-Breadth) |
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Course Description
This course is the first semester of Organic Chemistry, a two-semester course, which includes topics on the properties and reactions of aliphatic and aromatic organic compounds. Emphasis is placed on the reaction mechanisms, fundamental principles, and modern instrumental methods. PREREQUISITE: CHEM C185. Transfer Credit: CSU; UC: Credit Limitations: no credit for CHEM C110 if taken after CHEM C180 or CHEM C220; no credit for CHEM C130 if taken after CHEM C180 or CHEM C220; no credit for CHEM C140, PHYS C140 if taken after CHEM C180 or CHEM C220. C-ID: CHEM 150, CHEM 160 S.C-ID: CHEM 150, CHEM 160 S.
Course Level Student Learning Outcome(s)
- Deduce the structure of organic molecules using infrared and NMR spectroscopy
- Apply Lewis structural theory, VSEPR theory, molecular orbital theory, resonance structures, and polarity to represent organic molecules.
- Use IUPAC nomenclature rules to provide a systematic name for a chemical structure or derive chemical structure from the systematic name for alkanes, alkyl halides, alkenes, alkynes, alcohols, and esters.
- Identify the anticipated products of substitution (SN1 and SN2) and elimination reactions (E1 and E2) and the factors that influence them
- Explain the stereochemistry for reactions, including nucleophilic substitution, elimination, alkene additions, alkyne additions, and free-radical halogenations.
- Use Fischer projections to represent chiral centers and apply the R/S system to name enantiomers.
Course Objectives
- 1. Apply principles of electron configurations, Lewis structural theory, VSEPR Theory, and molecular orbital theory to predict the structure, bonding, and three-dimensional shapes of organic molecules.
- 2. Use IUPAC nomenclature rules to provide systematic names for chemical structures or sketch the appropriate chemical structure from a systematic name for organic molecules
- 3. Illustrate reaction mechanisms using curved-arrow notation and predict the expected products, including stereoisomers, for common organic reactions, including nucleophilic substitution, elimination, addition, oxidation, and reduction reactions.
- 4. Interpret infrared, 1H and 13C NMR spectra of organic compounds.
Lecture Content
Review of structure and bonding Electron configurations, Lewis dot structures, VSEPR, hybrid orbitals Bronsted-Lowry acids and bases; Lewis acids and bases Functional Groups Infrared Spectroscopy Alkanes and Cycloalkanes Nomenclature Conformational Analysis Stability Chirality Optical activity, R/S configurations, Enantiomers and diastereomers; racemic mixtures Stereospecific chemical reactions Alkyl Halides Nomenclature and reaction chemistry Nucleophilic Substitution Reactions SN1 vs. SN2 Effects of Solvent, nucleophile, leaving group, alkyl substitution Elimination Reactions E1 vs. E2 Stereochemical considerations Alkenes Nomenclature, isomerism Addition Reactions Alkynes Nomenclature Addition reactions; acidity NMR Spectroscopy Chemical shift, integration, splitting patterns Mass Spectrometry Fragmentation patterns Alcohols and Ethers Reaction Chemistry
Method(s) of Instruction
- Lecture (02)
- DE Live Online Lecture (02S)
- DE Online Lecture (02X)
Instructional Techniques
Lecture Group Problem-solving exercises Computer-generated molecular modeling
Reading Assignments
Reading textbook selections prior to lectures Conducting literature research to gather information about spectroscopic data
Writing Assignments
Weekly Homework exercises including detailed explanations of reaction pathways
Out-of-class Assignments
Internet research for applications of lecture topics
Demonstration of Critical Thinking
Problem-solving exercises
Required Writing, Problem Solving, Skills Demonstration
Homework assignments, quizzes and exams consist of problem-solving exercises
Eligible Disciplines
Chemistry: Masters degree in chemistry OR bachelors degree in chemistry or biochemistry AND masters degree in biochemistry, chemical engineering, chemical physics, physics, molecular biology, or geochemistry OR the equivalent. Masters degree required.
Textbooks Resources
1. Required Wade, Leory G. Organic Chemistry, 9th ed. Upper Saddle River: Pearson , 2017 Rationale: -
Other Resources
1. Coastline Library