Organic Chemistry 2 - Practice

Adatok

A Tantárgybejelentőben megadott hivatalos adatok az alábbi tanévre: 2020-2021

Tematika

The aims of this course are to introduce students into several basic laboratory techniques and to demonstrate some characteristic reactions of organic compounds with various functional groups.

Előadások

Gyakorlatok

• 1. General instructions for work in the laboratory, safety precautions; Purification of benzaldehyde, synthesis of benzoin.
• 2. General instructions for work in the laboratory, safety precautions; Purification of benzaldehyde, synthesis of benzoin.
• 3. General instructions for work in the laboratory, safety precautions; Purification of benzaldehyde, synthesis of benzoin.
• 4. Synthesis of 2,6-dibenzylidene-cyclohexanone; Characteristic tube reactions of oxo compounds.
• 5. Synthesis of 2,6-dibenzylidene-cyclohexanone; Characteristic tube reactions of oxo compounds.
• 6. Synthesis of 2,6-dibenzylidene-cyclohexanone; Characteristic tube reactions of oxo compounds.
• 7. Synthesis of benzil; Identification of 4th unknown compound.
• 8. Synthesis of benzil; Identification of 4th unknown compound.
• 9. Synthesis of benzil; Identification of 4th unknown compound.
• 10. Characteristic tube reactions of carbohydrates; Preparation of oxalic acid, isolation of citric acid.
• 11. Characteristic tube reactions of carbohydrates; Preparation of oxalic acid, isolation of citric acid.
• 12. Characteristic tube reactions of carbohydrates; Preparation of oxalic acid, isolation of citric acid.
• 13. Acetylation of glucose; Identification of 5th unknown compound;
• 14. Acetylation of glucose; Identification of 5th unknown compound;
• 15. Acetylation of glucose; Identification of 5th unknown compound;
• 16. 1st written test; Synthesis of aspirin. Polarimetry.
• 17. 1st written test; Synthesis of aspirin. Polarimetry.
• 18. 1st written test; Synthesis of aspirin. Polarimetry.
• 19. Synthesis of lidocain (1st step); Characteristic tube reactions of carboxylic acids and carboxylic acid derivatives.
• 20. Synthesis of lidocain (1st step); Characteristic tube reactions of carboxylic acids and carboxylic acid derivatives.
• 21. Synthesis of lidocain (1st step); Characteristic tube reactions of carboxylic acids and carboxylic acid derivatives.
• 22. Synthesis of lidocain (2nd step);
• 23. Synthesis of lidocain (2nd step);
• 24. Synthesis of lidocain (2nd step);
• 25. Synthesis of heterocycles I. (five membered): benzimidazole, dilantin; Characteristic tube reactions of pyridine.
• 26. Synthesis of heterocycles I. (five membered): benzimidazole, dilantin; Characteristic tube reactions of pyridine.
• 27. Synthesis of heterocycles I. (five membered): benzimidazole, dilantin; Characteristic tube reactions of pyridine.
• 28. Synthesis of heterocycles II. (six membered): 4-phenyl-5-carbethoxy-6-methyl-1,2,3,4-tetrahyropyrimidin-2-one, 4-methyl-7-hydroxycoumarine.
• 29. Synthesis of heterocycles II. (six membered): 4-phenyl-5-carbethoxy-6-methyl-1,2,3,4-tetrahyropyrimidin-2-one, 4-methyl-7-hydroxycoumarine.
• 30. Synthesis of heterocycles II. (six membered): 4-phenyl-5-carbethoxy-6-methyl-1,2,3,4-tetrahyropyrimidin-2-one, 4-methyl-7-hydroxycoumarine.
• 31. 2nd written test. Isolation of caffeine.
• 32. 2nd written test. Isolation of caffeine.
• 33. 2nd written test. Isolation of caffeine.
• 34. Isolation of quercetin and myristic acid.
• 35. Isolation of quercetin and myristic acid.
• 36. Isolation of quercetin and myristic acid.
• 37. Characteristic tube reactions of amino acids and peptides.
• 38. Characteristic tube reactions of amino acids and peptides.
• 39. Characteristic tube reactions of amino acids and peptides.
• 40. Evaluation.
• 41. Evaluation.
• 42. Evaluation.

Szemináriumok

A tananyag elsajátításához szükséges segédanyagok

Kötelező irodalom

Saját oktatási anyag

Kálai, T., Bognár, B. Organic Chemisry Laboratory Manual, Dept. of Org. and Med. Chem., Medical Faculty, University of Pécs, 2010.

Jegyzet

Ajánlott irodalom

Charles F. Wilcox, Jr., Mary F. Wilcox: Experimental Organic Chemistry: a Small-scale Approach, 2nd ed., Prentice-Hall, London, 1995.
Dana W. Mayo, Ronald M. Pike, Peter K. Trumper: Microscale Organic Laboratory with Multistep and Multiscale Syntheses, 3rd ed., Wiley, New York, 1994.

A félév elfogadásának feltételei

Maximum of 25 % absence allowed

Félévközi ellenőrzések

The organic chemistry laboratory course will be graded (1-5), based on the two written tests on 6th and 11th week, first of all. The evaluation can be modified by grades of semi-micro preparations, success of unknown identification as well as the outlook of the records of exercise book.

Távolmaradás pótlásának lehetőségei

Students have to contact their lab TA within 48 hours of missing lab to make the necessary arrangements.

Vizsgakérdések

The written tests will contain the matter of practice.

Vizsgáztatók

Gyakorlatok, szemináriumok oktatói

• Dr. Bognár Balázs
• Dr. Kálai Tamás