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COURSE INFORMATION
Course CodeCourse TitleL+P HourSemesterECTS
KIM 443STEREOCHEMISTRY2 + 07th Semester3,5

COURSE DESCRIPTION
Course Level Bachelor's Degree
Course Type Elective
Course Objective The main objectives of this course are twofold: to provide the student with a clear and logical presentation of the basic .
Course Content İsomerism: structure isomerisms and stereoisomerism,Enantiomers, Asymmetric molecules and asymmetric carbon atom, Nomenclature of enantiomers; Systems of R-S, Properties of enantiomers, Optic activity, Plane-polarized light, Polarimetry, Specific çevirme,Rasemic form, Optical purity, Synthesis of enantiomers, Rasemic resolution,Compounds with more than one stereo center. .
Prerequisites No the prerequisite of lesson.
Corequisite No the corequisite of lesson.
Mode of Delivery Face to Face

COURSE LEARNING OUTCOMES
1With knowledge of basic sciences, this course uses a combination of learned.
2Analyze the data, and evaluate in relation to the subject.
3Teaches the scientific method and research skills
4Course of vocational qualification and current issues related to the comments.
5Contemporary methods, techniques and analysis tools used in practice.
6Atoms and molecules in space due to differences in the basic principles of stereochemistry yönleniş learn the properties of stereoisomers.
7Finding indicates that the symmetry and chiral centers.
8Stereochemistry of organic compounds and their reactions, their point of view evaluate angle.
9What types of information contained in the grasp of science is another can distinguish
10I use the course content, assessment of current issues
11Experimental design and analyze the data.

COURSE'S CONTRIBUTION TO PROGRAM
PO 01PO 02PO 03PO 04PO 05PO 06PO 07PO 08PO 09PO 10PO 11PO 12PO 13PO 14PO 15PO 16PO 17
LO 0015                
LO 002  4              
LO 003 4     3         
LO 004                 
LO 005                 
LO 006                 
LO 007                 
LO 008     5           
LO 009          4      
LO 010                 
LO 011   4             
Sub Total5444 5 3  4      
Contribution00000000000000000

ECTS ALLOCATED BASED ON STUDENT WORKLOAD BY THE COURSE DESCRIPTION
ActivitiesQuantityDuration (Hour)Total Work Load (Hour)
Course Duration (14 weeks/theoric+practical)14228
Hours for off-the-classroom study (Pre-study, practice)14228
Mid-terms11717
Final examination11818
Total Work Load

ECTS Credit of the Course






91

3,5
COURSE DETAILS
 Select Year   


 Course TermNoInstructors
Details 2018-2019 Fall1ÇİĞDEM ŞAHİN
Details 2017-2018 Fall1AYKUT DEMİRÇALI
Details 2016-2017 Fall1ÇİĞDEM ŞAHİN
Details 2015-2016 Fall1ÇİĞDEM ŞAHİN
Details 2014-2015 Fall1ÇİĞDEM ŞAHİN
Details 2013-2014 Fall1İZZET ŞENER
Details 2012-2013 Fall1İZZET ŞENER
Details 2011-2012 Fall1İZZET ŞENER
Details 2010-2011 Fall1İZZET ŞENER
Details 2008-2009 Fall1RAFET KILINÇARSLAN
Details 2007-2008 Fall1FİKRET KARCI
Details 2006-2007 Fall1İZZET ŞENER
Details 2006-2007 Fall1FİKRET KARCI
Details 2005-2006 Fall1FİKRET KARCI
Details 2002-2003 Fall1MEHMET KARAKUŞ
Details 2002-2003 Fall1FİKRET KARCI


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Course Details
Course Code Course Title L+P Hour Course Code Language Of Instruction Course Semester
KIM 443 STEREOCHEMISTRY 2 + 0 1 Turkish 2018-2019 Fall
Course Coordinator  E-Mail  Phone Number  Course Location Attendance
FEN A0312 %60
Goals The main objectives of this course are twofold: to provide the student with a clear and logical presentation of the basic .
Content İsomerism: structure isomerisms and stereoisomerism,Enantiomers, Asymmetric molecules and asymmetric carbon atom, Nomenclature of enantiomers; Systems of R-S, Properties of enantiomers, Optic activity, Plane-polarized light, Polarimetry, Specific çevirme,Rasemic form, Optical purity, Synthesis of enantiomers, Rasemic resolution,Compounds with more than one stereo center. .
Topics
WeeksTopics
1 isomer and Isomer Compounds
2 geometric isomer in Alkanes
3 forms of the open-chain compounds
4 forms of the ring compounds
5 conformers of cyclohexane
6 chirality
7 rotating of the plane of polarized light
8 determination of configuration ​​R, S and D, L
9 The properties of the enantiomers
10 Optical activity and plane polarized light, polarimeter, specific rotation,
11 More asymmetric carbon
12 front chirality
13 splitting racemic mixtures
14 Atropisomerism
Materials
Materials are not specified.
Resources
Course Assessment
Assesment MethodsPercentage (%)Assesment Methods Title
Final Exam50Final Exam
Midterm Exam50Midterm Exam
L+P: Lecture and Practice
PQ: Program Learning Outcomes
LO: Course Learning Outcomes