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:	4
8	Theoretical (hour/week):	3
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. NEVİN ARIKAN ÖLMEZ
16	Course Lecturers:	Prof. Dr. Necdet COŞKUN, Doç. Dr. Nevin ARIKAN ÖLMEZ
17	Contactinformation of the Course Coordinator:	mtavasli@uludag.edu.tr +90 224 29 41 731 Uludağ Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümü, 16059 Görükle / BURSA, TÜRKİYE
18	Website:
19	Objective of the Course:	The aim of the course is being able to make the classification of organic compounds and know the examples of these classes.
20	Contribution of the Course to Professional Development

Learning Outcomes:

1	Learning the basic organic chemistry terms ;
2	Realizing the general properties of organic compounds ;
3	Learning the risks about organic compounds (personal and environmental) and using the chemicals carefully;
4	Being able to link some organic functional groups with textile ;

22	Course Content:

Week	Theoretical	Practical
1	Alkanes Molecule Geometry and Bond Angle Dash, Condensed and Bond-Line Formulas Aliphatic Alkanes (Methane, ..... Decane)
2	Alkyl Groups: General Formula Methyl, ethyl, n-propil, n-buthyl, n-pentil, n-hekzil,....n-desil İso-propil, sec-butyl, tert-butyl, sec-pentyl, neopentyl
3	Branched alkanes: Structural isomery Systematical nomenclature
4	Alcohols and Ethers: Water molecule Molecular Geometry and Bond Angle Alcoholes: Dash, Condensed and Bond-Line Formulas Primer, seconder and tertier alcoholes Mono and polialcoholes, Systematical nomenclature Intermolecular Forces (H-Bond) Ethers: Dash, Condensed and Bond-Line Formulas Structural isomery Intermolecular Forces (Dipole-Dipole Interactions)
5	Aminles: Ammonia Molecule Molecular Geometry and Bond Angle Dash, Condensed and Bond-Line Formulas Primer, seconder, tertier and quaternery amines Structural isomery Mono and poliamines, Systematical nomenclature Intermolecular Forces (H-Bond or Dipole-Dipole Interactions)
6	Aldehides and Ketones: Carbonyl Group Molecular Geometry and Bond Angle Aldehide: Dash, Condensed and Bond-Line Formulas Systematical nomenclature Ketones: Dash, Condensed and Bond-Line Formulas Systematical nomenclature Structural isomery Intermolecular Forces (Dipole-Dipole Interactions) (Aldose and Ketose sugars)
7	Carboxylic acids and Esters: Carbonyl, Hydroxyl and Alkoxy Groups Molecular Geometry and Bond Angle Carboxylic acids : Dash, Condensed and Bond-Line Formulas Systematical nomenclature Mono and policarboxylic acids Intermolecular Forces (H-Bond) Esters: Dash, Condensed and Bond-Line Formulas Systematical nomenclature Intermolecular Forces (Dipole-Dipole Interactions) Plantal and animal oils, and vaxes
8	Amidles: Carbonyl, Hydroxyl and Amide Groups Molecular Geometry and Bond Angle Dash, Condensed and Bond-Line Formulas Systematical nomenclature Intermolecular Forces (H-Bond and Dipole-Dipole Interactions) (Amino Acids, Proteinsr and Peptide Bonds)
9	Alkenles: Molecular Geometry and Bond Angle Dash, Condensed and Bond-Line Formulas Systematical nomenclature Geometrical Izomery (Cis-/Trans-Isomery) Intermolecular Forces (Van der Waals Interactions) Plantal Fatty Acids
10	Aromatic Compounds: Aromaticity Benzenoid Aromatic Compounds Heterocyclic Aromatic Compounds Ortho-/meta-/para-positions
11	Funtional Group Transformations: Determining the oxidation State Elektronegativity (C, H, O, Cl, Br)
12	Reduction Reaction: Reductive Reactants Oxidation Reaction: Oxidative Reactants
13	Acid-Base Reactions: Descriptions of Acid and Base Weak Acids Stronge Acids Buffer solutions
14

23	Textbooks, References and/or Other Materials:	G. Solomons ve C. Fryhle (Çev. Ed. G. Okay ve Y. Yıldırır), Organik Kimya, Literatür Yayınları, 2002. J. McMurry, Organic Chemistry, Brooks/Cole Publishing Comp., 1992. P. Y. Bruice, Organic Chemistry, Prentice Hall, 2001. R. J. Fessenden ve J. S. Fessenden (Çev. Ed. T. Uyar), Organik Kimya, Güneş Kitabevi, 1992.
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

ECTS / WORK LOAD TABLE

Activites	NUMBER	TIME [Hour]	Total WorkLoad [Hour]
Theoretical	14	2	28
Practicals/Labs	0	0	0
Self Study and Preparation	14	0,5	7
Homeworks, Performances	0	0	0
Projects	0	0	0
Field Studies	0	0	0
Midtermexams	1	24	24
Others	0	0	0
Final Exams	1	34	34
Total WorkLoad			93
Total workload/ 30 hr			3,1
ECTS Credit of the Course			3

CONTRIBUTION OF LEARNING OUTCOMES TO PROGRAMME QUALIFICATIONS

	PQ1	PQ2	PQ3	PQ4	PQ5	PQ6	PQ7	PQ8	PQ9	PQ10	PQ11	PQ12	PQ13	PQ14	PQ15	PQ16
LO1	5	1	1	1	4	1	2	5	2	4	2	1	2	1	3	5
LO2	5	1	1	2	4	1	2	5	2	4	2	1	2	1	3	5
LO3	5	3	2	1	3	1	2	4	2	4	2	1	2	3	3	5
LO4	4	3	2	1	3	1	2	5	2	4	2	1	2	1	3	5

LO: Learning Objectives

PQ: Program Qualifications

Contribution Level:

1 Very Low

2 Low

3 Medium

4 High

5 Very High