PřF:C3060 Organic Chemistry-lab.course - Course Information

C3060 Organic Chemistry - laboratory course

Extent and Intensity

0/0/7. 7 credit(s). Recommended Type of Completion: graded credit. Other types of completion: z (credit).

Teacher(s)

RNDr. Slávka Janků, Ph.D. (seminar tutor)
Mgr. Jaromír Literák, Ph.D. (seminar tutor)
RNDr. Stanislav Man, Ph.D. (seminar tutor)
Ing. Alena Pálková (seminar tutor)

Guaranteed by

RNDr. Slávka Janků, Ph.D.
Department of Chemistry – Chemistry Section – Faculty of Science
Contact Person: RNDr. Slávka Janků, Ph.D.

Timetable

Mon 7:00–13:50 MP1,01014, Tue 7:00–13:50 MP1,01014, Wed 7:00–13:50 MP1,01014, Thu 7:00–13:50 MP1,01014, Fri 7:00–13:50 MP1,01014

Prerequisites

C1080; You have to pass tests of your knowledge.

Course Enrolment Limitations

The course is also offered to the students of the fields other than those the course is directly associated with.

fields of study / plans the course is directly associated with

there are 25 fields of study the course is directly associated with, display

Course objectives

Fundamental laboratory methods of organic chemistry for synthesis (heating, stirring, cooling, introduction of gases, working with decrease of pressure, drying) and separation of organic compounds (filtering, crzstallization, distillation, extraction). The methods are trained an the compounds synthesis of important types of organic reactions. The products are characterized bz melting point, thin-layer chromathography, refractive index, and infra-red spectroscopy.

Syllabus

• 1. a) Ethyl bromide (SN2 mechanism, distillation) b) tert-Butyl chloride (SN1 mechanism, distillation) 2. 3-Phenylpropanoic acid (Catalytic hydrogenation, work with hydrogen, recrystallization, work with rotary evaporator) 3. Phenole nitration(SEAr mechanism , steam distillation , recrystallization) 4. Azobenzene (electrochemical reduction, recrystallization, TLC) 5. Ethyl 3-oxobutanoate ethylenacetale(AN mechanism to C=O, azeotropic and vacuum distillation, work with rotary evaporator) 6. a) 4,4-diphenyl-4-hydroxy-2-butanone ethylenacetale (AN mechanism to C=O, extraction, work with rotary evaporator, recrystallization) b) 4,4-Diphenyl-4-hydroxy-2-butanone (acid catalyzed hydrolysis of acetale, extraction, work with rotary evaporator, recrystallization) 7. 3-Nitroacetophenone (SEAr mechanism , recrystallization, IR spectroscopy) 8. a) 1-(3-Nitrophenyl)ethanol (selective reduction, extraction, recrystallization, IR spectroscopy) b) 3-Aminoacetophenone (selective reduction, recrystallization, IR spectroscopy) 9. Pinacol (metal reduction in anhydrous non-polar solvents, work with rotary evaporator) 10. Benzoic acid(AN to C=O, work with anhydrous solvents, extraction, sublimation) 11. Anthranilic acid (Hofmannovo odbourávání amide, recrystallization) 12. Ethyl-acetate (esterifikace, distillation) 13. 2-Hydroxy-5-methyl-2'-nitroazobenzene (diazotization and diazonium coupling, recrystallization, TLC) 14. 2-(2-Hydroxy-5-methylfenyl)benzotriazol (biochemical reductive cyclization, extraction, work with rotary evaporator, recrystallization) 15. 2-chlorbenzoic acide (diazotisation a Sandmayer reakction, recrystallization) Every student have to pass at least 14 practices. Practice 3, 5, 6, 7, 10 a 15 are required.

Literature

• NOVÁČEK, Eduard and Milan POTÁČEK. Laboratorní technika ke cvičení z metod organické chemie. Edited by Slávka Janků. 1. vyd. Brno: Masarykova univerzita, 1997, 91 s. ISBN 8021015004. info

Assessment methods (in Czech)

Laboratorní cvičení ukončené klasifikovaným zápočtem.

Language of instruction

Czech

Further comments (probably available only in Czech)

Study Materials
The course is taught annually.
General note: Vyučují učitelé katedry organické chemie.

Teacher's information

http://koch.chemi.muni.cz/

• Enrolment Statistics (Autumn 2006, recent)
  
• Permalink: https://is.muni.cz/course/sci/autumn2006/C3060