COURSE SYLLABUS

CARBONION CHEMISTRY

1	Course Title:	CARBONION CHEMISTRY
2	Course Code:	KIM4011
3	Type of Course:	Optional
4	Level of Course:	First Cycle
5	Year of Study:	4
6	Semester:	7
7	ECTS Credits Allocated:	5
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 Prof. Dr. Mustafa Tavaslı
17	Contactinformation of the Course Coordinator:	narikan@uludag.edu.tr +90 224 29 41 731 Uludağ Üniversitesi, Fen-Edebiyat Fakültesi, Kimya Bölümü, 16059 Görükle / BURSA,
18	Website:
19	Objective of the Course:	The aim of the course is to provide information about properties, synthesis, reactions and applications of carbonyl compounds and derivatives, amines and phenols.
20	Contribution of the Course to Professional Development

Learning Outcomes:

1	Learning the general properties and applications of organic compounds such as carbonyl compounds and derivatives, amines and phenols.;
2	Learning the methods of synthesis of these compounds.;
3	Comprehending and being construe of the basic reaction mechanisms.;
4	Earning the ability of planning and designing the synthesis reactions having steps of some organic compounds;

22	Course Content:

Week	Theoretical	Practical
1	Carboxyclic acids Description and general properties, synthesis and reactions of carboxyclic acids. Classification of the carboxyclic acid derivatives (acid chloride, ester, acid anhydride, amide, nitrile compounds). Efficiency range of carboxyclic acid derivatives
2	Acid chlorides and Anhydrides Description, nomenclature, and general properties, synthesis and reactions of acid chlorides Description, nomenclature and general properties, synthesis and reactions of acid anhydrides
3	Esters Description, nomenclature, and general properties, synthesis and reactions of esters Hydrolysis reaction of esters in acidic and basic mediums. Synthesis of cyclic ester compounds (lactone)
4	Amides Description, nomenclature, and general properties , base properties, synthesis and reactions of amides. Reduction of amides. Synthesis of cyclic amide compounds
5	Nitriles Description, nomenclature, and general properties, synthesis and reactions of nitriles. Synthesis of carboxylic acid from nitrile compounds
6	Conjugated diene systems Description and general properties of conjugated diene systems. Stability of conjugated dienes. Description of MO. 1,2 and 1,4- additions to conjugated diene systems. 1,4 cycloaddition reactions of conjugated dienes (Diels-Alder reaction and its general principles)
7	Carbonyl Alpha-Substitution Reaction Keto-Enole tautomerism: Formation of enole and enolate. Stability of the enolate structures. Acidity of alpha-hydrogens Reactions of Enoles: Alpha-halogenation of Aldehydes and ketone. Alpha-bromination of carboxylic acids
8	Problem solving Midterm Exam
9	Reactions of Enolate Ions: Alkylation of enolate ion. Halogenation of enolate ion. Selenization of enolat ion
10	Carbonyl Condensation Reactions Aldole condensation reaction-between Aldehyde and ketones. Claisen condensation reaction-between esters. Knoevenagel condensation reaction-between diethyl malonate/Malononitrile and Aldehyde/Ketone
11	Phenol, Aniline and Aryl halogenides Electrophilic aromatic substitution reactions. Nucleophilic aromatic substitution reactions. Acid-base reactions
12	Aliphatic Amines Nomenclature and physical properties Basicity of amines. Synthesis of Amines.
13	Reactions of amines
14	Polycyclic and Heterocyclic Compounds Samples and applications to polycyclic and heterocyclic compounds. Reactions and synthesis methods of polycyclic and hetrocyclic compounds

23	Textbooks, References and/or Other Materials:	1) G. Solomons ve C. Fryhle (Çev. Ed. G. Okay ve Y. Yıldırır), Organik Kimya, Literatür Yayınları, 2002. 2) R. J. Fessenden ve J. S. Fessenden (Çev. Ed. T. Uyar), Organik Kimya, Güneş Kitabevi, 1992. 3) J. McMurry, Organic Chemistry, Brooks/Cole Publishing Comp., 1992. 4) P. Y. Bruice, Organic Chemistry, Prentice Hall, 2001.
24	Assesment

TERM LEARNING ACTIVITIES	NUMBER	PERCENT
Midterm Exam	1	25
Quiz	1	15
Homeworks, Performances	0	0
Final Exam	1	60
Total	3	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	3	42
Practicals/Labs	0	0	0
Self Study and Preparation	13	1,5	19,5
Homeworks, Performances	0	0	0
Projects	0	0	0
Field Studies	0	0	0
Midtermexams	1	24	24
Others	1	24	24
Final Exams	1	48	48
Total WorkLoad			157,5
Total workload/ 30 hr			5,25
ECTS Credit of the Course			5

CONTRIBUTION OF LEARNING OUTCOMES TO PROGRAMME QUALIFICATIONS

	PQ1	PQ3	PQ5	PQ7
LO1	5	0	5	0
LO2	0	5	0	0
LO3	0	0	0	5
LO4	0	5	0	5

LO: Learning Objectives

PQ: Program Qualifications

Contribution Level:

1 Very Low

2 Low

3 Medium

4 High

5 Very High