COURSE UNIT TITLE

: ORGANIC CHEMISTRY II

Description of Individual Course Units

Course Unit Code Course Unit Title Type Of Course D U L ECTS
KIM 2106 ORGANIC CHEMISTRY II COMPULSORY 2 2 0 3

Offered By

Chemistry Teacher Education

Level of Course Unit

First Cycle Programmes (Bachelor's Degree)

Course Coordinator

PROFESSOR DOCTOR GÜLTEN ŞENDUR

Offered to

Chemistry Teacher Education

Course Objective

The aim of this course is to teach the basic concepts of aromatic compounds and organic molecules with functional groups, and to examine the chemical reactions and synthesis of these molecules.

Learning Outcomes of the Course Unit

1   To be able to explain the conditions of being aromatic.
2   To be able to distinguish the chemical reactions of alcohols and ethers.
3   To be able to distinguish chemical reactions of aldehydes and ketones.
4   To be able to distinguish the chemical reactions of carboxylic acids and their derivatives.
5   To be able to propose synthesis of carboxylic acids and their derivatives.

Mode of Delivery

Face -to- Face

Prerequisites and Co-requisites

None

Recomended Optional Programme Components

None

Course Contents

Week Subject Description
1 Aromaticity, benzene and substituted benzene
2 Electrophilic aromatic substitution reactions and mechanisms-1
3 Electrophilic aromatic substitution reactions and mechanism2 Chemical Properties of Alcohols-2 Aromaticity, benzene and substituted benzene Electrophilic aromatic substitution reactions and mechanisms-1 Electrophilic aromatic substitution reactions and mechanism2 Chemical Properties of Alcohols-1 Chemical Properties of Alcohols-2
4 Chemical Properties of Alcohols-1
5 Chemical Properties of Alcohols-2
6 Synthesis of Alcohols
7 Ethers-Epoxides: Chemical Properties- Synthesis
8 Midterm exam
9 Chemical Properties-Synthesis of Aldehydes
10 Chemical Properties-Synthesis of Ketones
11 Chemical Properties of Carboxylic Acids-1
12 Chemical Properties of Carboxylic Acids-2 Amides/Amines: Chemical Properties-Synthesis -1 Amides/Amines: Chemical Properties-Synthesis -2
13 Synthesis of Carboxylic Acids
14 Amides/Amines: Chemical Properties-Synthesis -1
15 Amides/Amines: Chemical Properties-Synthesis -2
16 Final Exam

Recomended or Required Reading

. G.Solomons, C.Fryhle, Organic Chemistry John Willey&Sons (2000)
2. H.Hart, D.J.Hart, L.E.Craine, Organic Chemistry Houghton Mifflin Company (1995)
3. R.J.Fessenden, J.S.Fessenden, Organic Chemistry Brooks/Cole Pub.Com. (2001)
4. R.C. Atkins, F.A. Carey, Organik Kimya Kısa ve Öz (Edt: Gürol Okay, Yılmaz Yıldırır) Bilim Yayınevi (2009)

Planned Learning Activities and Teaching Methods

Presentation, Discussion, Question-Answer technique

Assessment Methods

SORTING NUMBER SHORT CODE LONG CODE FORMULA
1 VZ Midterm
2 FN Semester final exam
3 BNS BNS Student examVZ * 0.40 + Student examFN * 0.60
4 BUT Make-up note
5 BBN End of make-up grade Student examVZ * 0.40 + Student examBUT * 0.60


Further Notes About Assessment Methods

None

Assessment Criteria

Assessment of the students will be done by using mid-term exam and final examination as can be seen from above gradings.

Language of Instruction

Turkish

Course Policies and Rules

Attendance to at least 70% for the lectures is an essential requirement of this course and is the responsibility of the student. It is necessary that attendance to the lecture and homework delivery must be on time. Any unethical behavior that occurs either in presentations or in exams will be dealt with as outlined in school policy. You can find the undergraduate policy at https://bef.deu.edu.tr/tr/

Contact Details for the Lecturer(s)

e-mail: gulten.sendur@deu.edu.tr

Office Hours

It will be annoced during the semester

Work Placement(s)

None

Workload Calculation

Activities Number Time (hours) Total Work Load (hours)
Lectures 14 2 28
Tutorials 14 2 28
Preparations before/after weekly lectures 14 1 14
Preparation for midterm exam 1 3 3
Preparation for final exam 1 5 5
Final 1 2 2
Midterm 1 2 2
TOTAL WORKLOAD (hours) 82

Contribution of Learning Outcomes to Programme Outcomes

PO/LOPO.1PO.2PO.3PO.4PO.5PO.6PO.7PO.8PO.9PO.10PO.11PO.12PO.13PO.14PO.15PO.16PO.17PO.18PO.19
LO.153
LO.253
LO.353
LO.453
LO.5533