The course provides fundamental knowledge in organic chemistry; .... 2000. John
McMurry. Organic. Chemistry. 5th ed. Thompson. Learning,. London. 1 ... J.R
Holum Fundamentals of. General, Organic and. Biological Chemistry. 6th. Edition
.
Course code
Course group
Volume in ECTS credits
Course hours
BBK 2004
C
6
160
Course type (compulsory or optional) Course level (study cycle) Semester the course is delivered Study form (face-to-face or distant)
Compulsory Bachelor Spring Face-to-face
Course title in Lithuanian ORGANINĖ CHEMIJA Course title in English ORGANIC CHEMISTRY Short course annotation in Lithuanian (up to 500 characters) Dalyko dėstymo metu pateikiama informacija: pagrindiniai organinės chemijos dėsniai; organinių junginių identifikacija; organinių junginių pavadinimų sudarymas; reakcijų mechanizmai bei jų tipai, cheminių reakcijų lygtys; cheminės jungties prigimtis; molekulių atomų sąveikos ypatumai. Supažindinama su galimais cheminių ryšių tipais priklausomai nuo substrato ir reagentų savybių bei reakcijos sąlygų. Short course annotation in English (up to 500 characters) The course provides fundamental knowledge in organic chemistry; identification of organic compounds; naming rules; reactions types/ mechanisms; chemical reactions of organic compounds. The course includes topics as: the origin of chemical bond; features of interaction between atoms; possible routes of chemical reactions in relationship with properties of substrate and reagents, reaction conditions. Prerequisites for entering the course
General Chemistry Course aim Introduction to the basis of organic chemistry Links between study programme outcomes and criteria of learning achievement evaluation Course outcomes Criteria of learning achievement evaluation Identify organic compound by its functional group; Students can classify organic compounds, can name it Naming organic compounds using IUPAC by IUPAC nomenclature nomenclature system Identify constitutional/ stereoisomers Students are able to identify isomers To know chemical bond types. Determine Students can identify chemical bond, determine type hybridization type of hybridization Students are able to describe induction and Describe induction and mesomerism mesomerism effects Indicate nucelophilic, electrophilic reagents. Know Students can indicate nucelophilic, electrophilic reaction types of organic compounds reagents. Know reaction types of organic compounds Identify organic compounds as Brønsted acids Students are able to identify compounds as Brønsted bases acids bases Be able to name alkanes, alkenes, alkines, to know Students are able to name alkanes, alkenes, alkines, its structure differences, synthesis paths and know its structure differences, synthesis paths and properties properties Identify chiral molecules, its asymmetric centre. To Students can identify molecule asymmetric centre, can know configuration type establishment rules. Name name enantiomers enantiomers Identify aromatic compounds. Describe effects of Students are able to describe aromaticity. Write substituent. Write nucleophilic substitution reactions reactions
To know synthesis paths and properties of the Students know synthesis paths and properties of the alcohols and phenols. alcohols and phenols. To write its synthesis reactions Write its synthesis reactions To write ethers, epoxydes, thiols and thioesters Students can write ethers, epoxydes, thiols and synthesis paths thioesters synthesis paths To know carbonyl compounds reaction mechanism, Students know the carbonyl compounds reaction structure, synthesis mechanism, structure, synthesis To name amino compounds, know its structure, Students can name amino compounds, know its synthesis, properties structure, synthesis, properties To know quintuple heterocycles synthesis paths, Students know quintuple heterocycles synthesis paths, chemical properties chemical properties To know indole, pyridine compounds synthesis and Students know indole, pyridine compounds synthesis its properties and its properties Content (topics) 1. Classification and nomenclature of organic compounds. 2. Spacial structure of organic compounds. 3. Atomic structure and origin of chemical bond. Covalent, hydrogen bonds and its properties. Geometry of the molecules. Atomic orbitals hybridization. Conjugation and resonance. 4. Typical electronic effects of organic compounds molecules. 5. Types of reagents and reactions. 6. Acids and bases. 7. Alkans. Alkenes Alkines. Halogenoalkanes. Cycloalkanes. 8. Chiral molecules and optic activity. Enantiomers. Configuration establishing rules. Diastereoisomers and racemates. Stereochemistry of the additional reactions of alkenes. 9. Benzene and aromaticity. Effects of substituents of aromatic compounds. Nucleophilic substitution in arenes. 10. Alcohols and phenols. 11. Ethers, epoxydes, thiols, thiolethers. 12. Carbonyl compounds. Carboxylic acids and its derivatives. Hydroxy-, oxo- and dicarboxylic acids. Carbon acid derivatives. 13. Amines. 14. Quintuple heterocycles (pyrol, furan, thiophene, imidazole) ring synthesis principles. Quintuple heterocycles chemical properties and reactivity differences. 15. Indole, synthesis and properties of its derivatives, reactions with electrophilic reagents. Pyridine, ring electronis structure, properties as a base. Synthesis of pyridine derivatives. Distribution of workload for students (contact and independent work hours) Lectures - 45 h., laboratory work - 30 h., individual student work - 78 h, knowledge test -7h. Structure of cumulative score and value of its constituent parts Mid-term exam - 20 %, laboratory work report and test - 30 %, final exam - 50 % Recommended reference materials No.
Publication year
1.
2002
2.
2000
3.
2000
Authors of publication and title V. Laurinavičius Organinė ir bioorganinė chemija T.W. Graham Solomons, Craig B. Fryhle. Organic Chemistry. 6th bei 7th ed. John McMurry. Chemistry. 5th ed.
Organic
Publishing house Basic materials Vilnius Mokslo ir enciklopedijų leidykla
University library 45
Wiley, New York
2
Thompson Learning, London
1
Number of copies in Self-study Other libraries rooms
2
4.
1995
5.
1999
6.
2006
1.
2006
2.
1998
3.
1988
4.
2002
R.Baltrušis, J.Degutis, G.Dienys, V.Mickevičius, Žodynas: A.Šačkus, P.Vainilavičius. Vilnius Organinė chemija. I d. R.Baltrušis, J.Degutis, G.Dienys, V.Mickevičius, Žodynas: A.Šačkus, P.Vainilavičius. Vilnius Organinė chemija. II d. Z.J. Beresnevičius, P.R. Kadziauskas. „Technologija“, Organinė Kaunas chemija. Uždavinynas Supplementary materials W.H., Brown, J March, Harcourt Introduction to General, College Organic & Biochemistry, 8th Publishers Edition by F.A. Bettelheim, J.R Holum Fundamentals of General, Organic and John Wiley & Biological Chemistry. 6th Sons Edition R. Šatinskienė ir kt. Organinės chemijos Vilnius laboratoriniai darbai Oxford Marc Loudon. Organic University Chemistry Press, OxfordNew York
24
2
24
2
48
1
1
1
48
1
Course programme designed by Doc. dr. Simona Sutkuvienė, Department of Biochemistry and Biotechnology, Faculty of Natural Sciences
