Department of...
 
Organic chemistry 2
 
Organic chemistry 2
 
Code: 40765
ECTS: 6.0
Lecturers in charge: izv. prof. dr. sc. Vesna Petrović Peroković - Lectures
Lecturers: Ivan Kodrin - Exercises
Take exam: Studomat
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1. komponenta

Lecture typeTotal
Lectures 60
Exercises 15
* Load is given in academic hour (1 academic hour = 45 minutes)
Description:
COURSE GOALS: Introduction to structure and reactivity of carbon compounds.

LEARNING OUTCOMES AT THE LEVEL OF THE PROGRAMME:
1. KNOWLEDGE AND UNDERSTANDING
1.2. demonstrate a thorough knowledge and understanding of the fundamental concepts in chemistry
1.4. demonstrate a thorough knowledge and understanding of the most important chemistry laws and theories laws and theories
2. APPLYING KNOWLEDGE AND UNDERSTANDING
2.2. describe important aspects of chemical change
5. LEARNING SKILLS
5.1. search for and use professional literature as well as any other sources of relevant information

LEARNING OUTCOMES SPECIFIC FOR THE COURSE:
Students will be able:
1. to represent organic molecules in space using structural formulae and give them names using IUPAC nomenclature
2. to write and to explain the mechanisms of elimination reactions, electrophilic additions on unsaturated and conjugated substrates, pericyclic reactions and electrophilic and nucleophilic aromatic substitution
3. explain the influence of structure on reactivity of organic molecules
4. to define aromaticity and antiaromaticity and explaine on examples
5. to plan a multistep synthesis of simple organic compounds on the basis of acquired knowledge in organic chemistry
6. to connect structure of biologically important molecules with their biological role.

COURSE DESCRIPTION:
1. Elimination reactions
1.1. Mechanisms and stereochemistry of elimination reactions
1.2. Elimination versus substitution
2. Electrophilic additions to unsaturated carbon
2.1. Mechanisms and stereochemistry of addition reactions
2.2. Addition to conjugated dienes and conjugated carbonyl compounds
2.3. Homogenic and heterogenic catalysis
3. Pericyclic reactions
3.1. (4 + 2) cycloaddition and dipolar cycloaddition
3.2. Orbital symetry control of pericyclic reactions (HOMO-LUMO and correlation diagram methods)
3.3. Electrocyclic reactions and sigmatropic rearrangements
4. Electrophilic aromatic substitutions
4.1. Aromatic and antiaromatic compounds
4.2. Mechanism of electrophilic aromatic substitution
4.3. Substituent effects on orientation in electrophilic aromatic substitution
4.4. Reactions of heteroaromatic compounds
5. Nucleophilic aromatic substitution
6. Molecular rearrangements
7. Free radical reactions
8. Organic synthesis
8.1. Design of a synthesis (starting materials, construction reactions, functional group
interconvesions and protecting groups)
8.2. Retro-synthetic approach
9. Natural organic compounds
9.1. Carbohydrates
9.2. Amino acids and proteins
9.3. Lipids
9.4. Alkaloids
9.5. Pheromones

REQUIREMENTS FOR STUDENTS:
Attendance to lectures and exercises.

GRADING AND ASSESSING THE WORK OF STUDENTS:
Written and oral final exam.
Literature:
  1. S. H. Pine, Organska kemija, Školska knjiga 1994.
  2. L. G. Wade: Organic Chemistry, 7. izdanje, Pearson Prentice Hall, NJ, SAD, 2010.
  3. J. Clayden, N. Greeves, S.Warren and P. Wothers, Organic Chemistry, Oxford University Press, 2001.
Prerequisit for:
Enrollment :
Attended : Physical Chemistry

Examination :
Passed : Organic chemistry 1
6. semester
Mandatory course - Mandatory studij - Physics and Chemistry Education
Consultations schedule:
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