Stereochemistry Course
This course builds expertise in stereochemistry, covering 3D molecular representations like wedge-dash, Fischer, and Newman projections. Students learn to assign R/S configurations using CIP rules, distinguish enantiomers, diastereomers, and meso compounds, and understand chirality's role in biological activity, especially drugs. It includes strategies for single-enantiomer synthesis, analytical techniques such as NMR and HPLC, and clear reporting for research and regulations, equipping learners for advanced chemistry applications.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
Gain mastery in 3D molecular representations and R/S assignments through practice with wedge-dash, Fischer, and Newman projections. Explore enantiomers, diastereomers, meso forms, and chirality's impact on biology. Develop skills in single-enantiomer synthesis, analytical methods like NMR and HPLC, and precise reporting for research and regulatory needs.
Elevify advantages
Develop skills
- Master 3D stereochemical drawings using wedge-dash, Fischer, and Newman projections.
- Assign R/S configurations quickly with CIP rules, dodging common errors.
- Analyze chiral drug effects linking enantiomers to binding, metabolism, toxicity.
- Design single-enantiomer syntheses via resolution, chiral pool, catalysis.
- Communicate stereochemistry in IUPAC names, SMILES, NMR, HPLC data.
Suggested summary
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