Print

COURSE INFORMATION
Course CodeCourse TitleL+P HourSemesterECTS
KIM 301ORGANIC REACTION MECHANISMS2 + 06th Semester3

COURSE DESCRIPTION
Course Level Bachelor's Degree
Course Type Compulsory
Course Objective This course will explain chemical structure, bond break species, acidity and basidity series. In addition, substitution, addition, elimination and rearrangement reactions will be presented.
Course Content Hybridisation and bond broken species, Nucleophilic substitution reactions, Pseudo and nucleophilic substitution reactions, Aromatic substitution reactions, Direction of double bond additive and hydrogen addition, Addition of carbonyl bonds and ozonation, Elimination reactions, Rearrangement reactions, Pericyclic reactions.
Prerequisites No the prerequisite of lesson.
Corequisite No the corequisite of lesson.
Mode of Delivery Face to Face

COURSE LEARNING OUTCOMES
1Will be able to use knowledge belonging fundamental science and learning from this course together
2Will be able to analyze data and evaluate to associate subject.
3Will be able to gain ability for scientific method and research
4Will be able to have technical ability and commend-follow actual subject
5Will be able to use necessary modern techniques and equipment in applications and analysis
6Will be able to write chemical reactions, develop the logic of writing reaction
7Will be able to commend organic reactions
8Will be able to display and query chemical reactions as a three-dimensional

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                 
LO 004  4              
LO 005   5             
LO 006     5 5         
LO 007          5      
LO 008                 
Sub Total5445 5 5  5      
Contribution11110101001000000

ECTS ALLOCATED BASED ON STUDENT WORKLOAD BY THE COURSE DESCRIPTION
ActivitiesQuantityDuration (Hour)Total Work Load (Hour)
Course Duration (14 weeks/theoric+practical)15230
Hours for off-the-classroom study (Pre-study, practice)10110
Mid-terms12323
Final examination11515
Total Work Load

ECTS Credit of the Course






78

3
COURSE DETAILS
 Select Year   


 Course TermNoInstructors
Details 2023-2024 Spring1AYKUT DEMİRÇALI
Details 2022-2023 Spring1AYKUT DEMİRÇALI
Details 2021-2022 Spring1AYKUT DEMİRÇALI
Details 2020-2021 Spring1AYKUT DEMİRÇALI
Details 2019-2020 Spring1AYKUT DEMİRÇALI
Details 2018-2019 Spring1AYKUT DEMİRÇALI
Details 2017-2018 Spring1AYKUT DEMİRÇALI
Details 2016-2017 Spring1ÇİĞDEM ŞAHİN
Details 2015-2016 Spring1ÇİĞDEM ŞAHİN
Details 2014-2015 Spring1ÖZLEM ÖZEN KARAKUŞ
Details 2013-2014 Spring1FİKRET KARCI
Details 2012-2013 Summer1HASALETTİN DELİGÖZ
Details 2012-2013 Summer1HASALETTİN DELİGÖZ
Details 2012-2013 Summer1HASALETTİN DELİGÖZ
Details 2012-2013 Spring1İZZET ŞENER
Details 2011-2012 Summer1İZZET ŞENER
Details 2011-2012 Spring1İZZET ŞENER
Details 2010-2011 Summer1HASALETTİN DELİGÖZ
Details 2010-2011 Spring2İZZET ŞENER
Details 2009-2010 Summer1HASALETTİN DELİGÖZ
Details 2009-2010 Fall3HASALETTİN DELİGÖZ
Details 2008-2009 Fall1FİKRET KARCI


Print

Course Details
Course Code Course Title L+P Hour Course Code Language Of Instruction Course Semester
KIM 301 ORGANIC REACTION MECHANISMS 2 + 0 1 Turkish 2023-2024 Spring
Course Coordinator  E-Mail  Phone Number  Course Location Attendance
Assoc. Prof. Dr. AYKUT DEMİRÇALI ademircali@pau.edu.tr FEN A0213 %
Goals This course will explain chemical structure, bond break species, acidity and basidity series. In addition, substitution, addition, elimination and rearrangement reactions will be presented.
Content Hybridisation and bond broken species, Nucleophilic substitution reactions, Pseudo and nucleophilic substitution reactions, Aromatic substitution reactions, Direction of double bond additive and hydrogen addition, Addition of carbonyl bonds and ozonation, Elimination reactions, Rearrangement reactions, Pericyclic reactions.
Topics
WeeksTopics
1 Conjugated pi bonds, 1,2- and 1,4- are added to 1,2-conjugated dienes
2 Diels-Alder reaction, 1,4- is added to alpha,beta-unsaturated carbonyl compounds
3 Acidity of alpha hydrogen, Alkylation of malonic ester
4 Alkylation of acetoacetic ester, The synthesies are made by alkylation reactions
5 Alkylation and acylation of enamines, aldol condensations
6 Ester condensations, Nucleophilic is added to alpha,beta unsaturated carbonyl compounds
7 Moleculer orbitals of conjugated polyenes, Cyclic addition reactions
8 Electrocyclic reactions
9 Sigmatropic rearrangement
10 Rearrangements by anion migration
11 Rearrangements to nitrogen atom
12 Rearrangements to oxsygene atom
13 Radicalic rearrangements
14 Rearrangements by cation migration
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