| Course Unit Title | Course Unit Code | Type of Course Unit | Level of Course Unit | Year of Study | Semester | ECTS Credits |
|---|---|---|---|---|---|---|
| Stereochemistry | KIM429 | Elective | Bachelor's degree | 4 | Fall | 5 |
Name of Lecturer(s)
Prof. Dr. Cavit UYANIK
Prof. Dr. Mehmet YILMAZ
Associate Prof. Dr. Selahaddin GÜNER
Learning Outcomes of the Course Unit
1) Explain three dimentional molecular structure of organic molecules
1) Explain three dimentional molecular structure of organic molecules
2) Separate stereoisomeric structures
2) Separate stereoisomeric structures
3) Explain the effect of stereochemical structures in organic reactions
3) Explain the effect of stereochemical structures in organic reactions
4) Explain stereochemical organic reactions
4) Explain stereochemical organic reactions
5) Read and write stereoisomeric structures
5) Read and write stereoisomeric structures
Program Competencies-Learning Outcomes Relation
| Program Competencies | |||||||||||||
| 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | ||
| Learning Outcomes | |||||||||||||
| 1 | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | |
| 1 | High | High | High | High | High | High | High | High | High | High | High | High | |
| 2 | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | |
| 2 | High | High | High | High | High | High | High | High | High | High | High | High | |
| 3 | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | |
| 3 | High | High | High | High | High | High | High | High | High | High | High | High | |
| 4 | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | |
| 4 | High | High | High | High | High | High | High | High | High | High | High | High | |
| 5 | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | No relation | |
| 5 | High | High | High | High | High | High | High | High | High | High | High | High | |
Mode of Delivery
Face to Face
Prerequisites and Co-Requisites
None
Recommended Optional Programme Components
absent
Course Contents
This course includes chirality, structure of molecules, isomerisms, enantiomers, symmetry plane and mirror image, optical activity, diastereomers and stereoisomers, sterochemical discriptors: D and L notation, R and S notation, alpha and beta notation, axial and equatorial positions, endo and exo definition, erythro and threo definition, syn-anti definition, cis-trans definition, E, Z definition, eclipced and staggered conformations, Gauche and Anti conformations, conformation of alkanes and cycloalkanes, conformational analysis, anomeric effects, stereochemical control asymmetric sythesis with chiral subsrate, conformational analysis with NMR spectroscopy.
Recommended or Required Reading
Planned Learning Activities and Teaching Methods
Assessment Methods and Criteria
Contribution of Midterm Examination to Course Grade |
40% |
|---|---|
Contribution of Final Examination to Course Grade |
60% |
Total |
100% |
Language of Instruction
English
Work Placement(s)
Not Required