PřF:C2021 Organic Chemistry I - Course Information
C2021 Organic Chemistry I
Faculty of ScienceSpring 2024
- Extent and Intensity
- 2/0/0. 2 credit(s) (plus extra credits for completion). Type of Completion: zk (examination).
- Teacher(s)
- doc. Mgr. Kamil Paruch, Ph.D. (lecturer)
Mgr. Jakub Švenda, PhD. (lecturer)
RNDr. Slávka Janků, Ph.D. (seminar tutor)
Mgr. Jaromír Literák, Ph.D. (seminar tutor) - Guaranteed by
- doc. Mgr. Kamil Paruch, Ph.D.
Department of Chemistry – Chemistry Section – Faculty of Science
Supplier department: Department of Chemistry – Chemistry Section – Faculty of Science - Timetable
- Mon 19. 2. to Sun 26. 5. Wed 10:00–11:50 B11/132
- Prerequisites
- ( C1020 General Chemistry || C1601 General and Inorg. Chemistry ) && !NOW( C2700 Basic Organic Chemistry )
Knowledge of General chemistry principles - 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
- Analytical Chemistry (programme PřF, N-CH)
- Inorganic Chemistry (programme PřF, N-CH)
- Physical Chemistry (programme PřF, N-CH)
- Chemistry (programme PřF, B-CH)
- Environmental Chemistry (programme PřF, N-CH)
- Molecular Biology and Genetics (programme PřF, B-EXB)
- Molecular Biology and Genetics (programme PřF, N-EXB)
- Organic Chemistry (programme PřF, N-CH)
- Course objectives
- In the course Organic Chemistry I, the students will learn main rules of nomenclature of organic compounds, basic piece of information about stereochemistry of organic molecules as well as important methods of structure investigation. They will also learn about the basic types of organic reactions, the ionic and radical ones, oxidations and reductions, and some of those controlled by symmetry of frontier orbitals. In the end of the course, the student will be able to draw the molecular structure correctly, to consider the reactivity in different situations, and to decide which reactions will run in common reaction systems.
- Learning outcomes
- After completion of the course students will be able to:
- Understand and apply the basic organic chemistry nomenclature;
- Utilize information of common methods used for structure determination in organic chemistry;
- Recognize the basic structure-reactivity relationships exploring the information about electronic structure, polarity and stereo configuration of organic molecules;
- Understand main types of organic reaction mechanisms and apply them to explain and predict the results of chemical transformations of basic types of organic compounds. - Syllabus
- 1. The scope of Organic Chemistry. Drawing organic molecules. Basic principles of nomenclature. Aliphatic and cyclic skeletons, hierarchy of functional groups. 2. Carbon atom bonding. Hybridization of atomic orbitals, bond angles. Electron structure of molecules, sigma and pi-bond. Molecular orbitals, conjugation and delocalization. Mesomeric effect and resonance structures. Polarity and polarizability, charge distribution in molecules. 3. Basics of organic stereochemistry. Drawing organic molecules. Isomers and stereoisomers. Conformation and configuration. Geometric isomerism of alkenes and cycloalkanes. Conformation of ethane, butane and cyclohexane. Symmetry and chirality. Cahn-Ingold-Prelog nomenclature. Fischer projection. 4. Organic structures determination methods (MS,NMR, IR, UV-Vis). 5. Chemical reactions. Homolysis and heterolysis. Classification of organic reactions according to structural change (S-A-E-R). Reaction mechanism - "Arrow pushing". Depiction of organic reaction. Kinetics and thermodynamics. 6. Acids and Bases. Broensted theory. Chemical equilibrium. pH, pKa. Strength of (organic) acids and bases. Electrophiles and nucleophiles. Lewis theory. Hard and Soft Acids and Bases (HSAB). 7. Oxidation reduction reactions.SN1 and SN2 mechanisms 8. Nucleophilic subtitution and elimination reactions (halogen derivatives, alcohols, amines). Reaction kinetics, rate determining reaction step, carbocations stability, reaction stereospecifity. 9. Nucleophilic addition on cabonyl group. Michael addition, keto-enol tautomerism, Adition-elimination mechanism. 10. Electrophilic addition reactions. Alkenes, alkynes. Radical addition and polymerization. Radical substitution. 1,2- and 1,4-addition reactions pf conjugated dienes. 11. Aromaticity. Electrophilic aromatic substitution. Nucleophilic substituon. 12. Reaction with conservation of orbytal symmetry. Pericyclic reactions. Diels-Alder rection.
- Literature
- recommended literature
- Mc Murry: Organická chemie, překlad z originálu 6. vydání, 2004, vydáno VUT Brno-nakladatelství VUTIUM a VŠCHT Praha, listopad 2007.
- not specified
- SVOBODA, Jiří a kol. Organická chemie I. VŠCHT Praha 2005. ISBN 978-80-7080-561-9.
- MCMURRY, John. Fundamentals of organic chemistry. 4th ed. Pacific Grove: Brooks/Cole publishing company, 1998, xxii, 566,. ISBN 0-534-35245-4. info
- Clayden, J, Greeves, N., Warren, S. Organic Chemistry , 2nd Edition, Oxford University Press Inc., New York., ISBN 978-0-19-927029-3
- SOLOMONS, T. W. Graham. Organic chemistry. 6th ed. New York: John Wiley & Sons, 1996, xxvii, 121. ISBN 0471013420. info
- ČERVINKA, Otakar. Chemie organických sloučenin. 1. vyd. Praha: Státní nakladatelství technické literatury, 1985, 1131 s. info
- ČERVINKA, Otakar. Chemie organických sloučenin. Vyd. 1. Praha: Státní nakladatelství technické literatury, 1987, 1052 s. info
- POTÁČEK, Milan, Ctibor MAZAL and Slávka JANKŮ. Řešené příklady z organické chemie (Problems and Solutions in Organic Chemistry). 2nd ed. Brno: Masarykova univerzita, 2008, 243 pp. ISBN 80-210-2274-4. info
- LITERÁK, Jaromír. Sbírka řešených příkladů k semináři z organické chemie. 1. vyd. Brno: Masarykova univerzita, 2012, 307 s. ISBN 9788021058101. info
- POTÁČEK, Milan. Organická chemie : pro biology. 1. vyd. Brno: Vydavatelství Masarykovy univerzity, 1995, 208 s. ISBN 8021011254. info
- Teaching methods
- lecture
- Assessment methods
- The course introduces into structure, stereochemistry and reactivity knowledge on the basic hydrocarbon skeletons. This knowledge is then tested in 3 tests during semester. Every of them is limited by 33 points. Only those who obtained in all that tests in total sum more than 50 point, may go for the final written examination. 60 points is minimum for passing the final examination.
- Language of instruction
- Czech
- Follow-Up Courses
- Further comments (probably available only in Czech)
- Study Materials
The course is taught annually.
General note: Doporučuje se zapsat Speciální seminář z Organické chemie I. - Listed among pre-requisites of other courses
- C2022 Organic Chemistry I - Seminar
NOW(C2021)||C2021 - C2700 Principles of Organic Chemistry
(C1601||C1601bf||C1020) && !C2021 && !C3022 && !C3050 && !NOWANY(C2021,C3022,C3050) - C3050 Organic Chemistry II
C2021 - C7410 Structure and Reactivity
((C1020&&C2021&&(C3022||C3050)&&(C4660||C3140||C3401)&&(C4020||C4402))&&NOW(C7415))||souhlas - C8435 Heterocyclic compounds
C2021 && C3022 - C8780 Photochemistry: From Concepts to Practice
C1020&&C2021&&C3050&&C4660&&C4020
- C2022 Organic Chemistry I - Seminar
- Enrolment Statistics (Spring 2024, recent)
- Permalink: https://is.muni.cz/course/sci/spring2024/C2021