Türkçe English Rapor to Course Content
COURSE SYLLABUS
ORGANIC CHEMISTRY
1 Course Title: ORGANIC CHEMISTRY
2 Course Code: KIM1080
3 Type of Course: Compulsory
4 Level of Course: First Cycle
5 Year of Study: 1
6 Semester: 2
7 ECTS Credits Allocated: 3
8 Theoretical (hour/week): 2
9 Practice (hour/week) : 0
10 Laboratory (hour/week) : 0
11 Prerequisites: None
12 Recommended optional programme components: None
13 Language: Turkish
14 Mode of Delivery: Face to face
15 Course Coordinator: Doç. Dr. AYHAN YILDIRIM
16 Course Lecturers: Prof. Dr. Necdet Coşkun
Doç. Dr. Mustafa Tavaslı
Doç. Dr. Nevin Arıkan Ölmez
17 Contactinformation of the Course Coordinator: yildirim@uludag.edu.tr
Tel: 0 (224) 294 1771
Uludağ Üniversitesi Fen-Edebiyat Fakültesi Kimya Bölümü, Görükle/BURSA 16059
18 Website:
19 Objective of the Course: The aim of the course is to teach the biologically important organic molecules contain functional groups, structural frame and tri-dimensional structural of organic molecules.
20 Contribution of the Course to Professional Development
21 Learning Outcomes:
1 Knowing of the Organic Chemistry and being aware of the importance in Biology.;
2 Learning of the basic Organic Chemistry terms.;
3 Learning the reactions of some basic Organic functional groups.;
4 Learning the physical and chemical properties of some organic compounds that being Biological important.;
5 Learning the bio-effectiveness and/or the bio-harmfulness of some organic compounds and using these with this consciousness ;
6 Being knowledgeable about the applications of some organic compounds existed in nature.;
22 Course Content:
Week Theoretical Practical
1 Alkanes: - Molecular geometry and Bond angle - Closed, Opened, Compressed and Lineer Formula - Straight chained Alkanes (Methane….Decan)
2 Alkyl Groups: -General Formula -Methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl…n-decyl -İsopropyl, sec-butyl, ter-butyl, sec-pentyl, neopentyl
3 Branched alkanes: -Structural isomerism -Systematic nomenclature
4 Alcohols and Ethers: -Water molecule -Molecular geometry and Bond angle Alcohols: -Closed, Opened, Compressed and Lineer Formula -Primary, secondary and tertiary alcohols -Mono and poly alcohols, Systematic nomenclature -Forces that holding the molecules together (H-Bond) Ethers: -Closed, Opened, Compressed and Lineer Formula -Structural isomerism -Forces that holding the molecules together (Dipole-dipole interaction)
5 Amines: -Ammonia molecule -Molecular geometry and Bond angle -Closed, Opened, Compressed and Lineer Formula -Primary, secondary tertiary and quarternary amines -Structural isomerism -Mono and polyamines, Systematic nomenclature -Forces that holding the molecules together (H-Bond and Dipole-dipole interaction)
6 Aldehydes and Ketones: -Carbonyl group -Molecular geometry and Bond angle Aldehydes: -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature Ketones: -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature -Structural isomerism -Forces that holding the molecules together (Dipole-dipole interaction) -Aldose and Ketose sugars
7 Carboxylic acids and Esters: -Carbonyl, Hydroxyl and Alcoxy groups -Molecular geometry and Bond angle Carboxylic acids: -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature -Mono and polycarboxylic acids -Forces that holding the molecules together (H-Bond) Esters: -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature -Forces that holding the molecules together (Dipole-dipole interaction) -Vegetable and animal oils and Waxs
8 Amides: -Carbonyl, Hydroxyl and Amide groups -Molecular geometry and Bond angle -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature -Forces that holding the molecules together (H-Bond or Dipole-dipole interaction) -Aminoacids, Proteins and Peptide bonds
9 Alkenes: -Molecular geometry and Bond angle -Closed, Opened, Compressed and Lineer Formula -Systematic nomenclature -Geometrical isomerism (Cis-Trans isomerism) -Forces that holding the molecules together (Van der Waals interaction) -Vegetable fatty acids
10 Aromatic compounds: -Aromaticity -Benzenoid Aromatic compounds -Heterocyclic Aromatic compounds -Ortho-/meta-/ para- positions
11 Functional group converisons: -Determination of oxidation step -Electronegativity (C, H, O, Cl, Br)
12 Reduction Reaction: -Reductive reagents
13 Oxidation Reaction: -Oxidative reagents
14 Acid-base reaction: -Description of acid and base -Poor acids -Strong acids -Buffer solutions
23 Textbooks, References and/or Other Materials: i) G. Solomons ve C. Fryhle (Çev. Ed. G. Okay ve Y. Yıldırır), Organik Kimya, Literatür Yayınları, 2002.
ii) R. J. Fessenden ve J. S. Fessenden (Çev. Ed. T. Uyar), Organik Kimya, Güneş Kitabevi, 1992.
iii) J. McMurry, Organic Chemistry, Brooks/Cole Publishing Comp., 1992.
iv) P. Y. Bruice, Organic Chemistry, Prentice Hall, 2001.
24 Assesment
TERM LEARNING ACTIVITIES NUMBER PERCENT
Midterm Exam 1 40
Quiz 0 0
Homeworks, Performances 0 0
Final Exam 1 60
Total 2 100
Contribution of Term (Year) Learning Activities to Success Grade 40
Contribution of Final Exam to Success Grade 60
Total 100
Measurement and Evaluation Techniques Used in the Course
Information
25 ECTS / WORK LOAD TABLE
Activites NUMBER TIME [Hour] Total WorkLoad [Hour]
Theoretical 14 3 42
Practicals/Labs 0 0 0
Self Study and Preparation 2 5 10
Homeworks, Performances 0 18 18
Projects 0 0 0
Field Studies 0 0 0
Midtermexams 1 20 20
Others 0 0 0
Final Exams 1 30 30
Total WorkLoad 120
Total workload/ 30 hr 4
ECTS Credit of the Course 4
26 CONTRIBUTION OF LEARNING OUTCOMES TO PROGRAMME QUALIFICATIONS
PQ1 PQ2 PQ3 PQ4 PQ5 PQ6 PQ7 PQ8 PQ9 PQ10 PQ11
LO1 5 0 0 5 0 4 0 0 0 0 0
LO2 0 0 0 5 0 0 0 0 0 0 0
LO3 0 0 0 5 0 0 0 0 0 0 0
LO4 0 0 0 5 0 0 0 0 0 0 0
LO5 0 0 0 0 0 5 0 0 0 0 0
LO6 0 0 0 5 0 0 0 0 0 0 0
LO: Learning Objectives PQ: Program Qualifications
Contribution Level: 1 Very Low 2 Low 3 Medium 4 High 5 Very High
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