Faculty of Science

Model (No 12)

Course Specification : كيمياء عضوية

2010 - 2011

 
Farabi Quality Management of Education and Learning - 24/11/2024
University :Mansoura University
Faculty :Faculty of Science
Department :Chemistry Department
1- Course data :-
Code: 48302
Course title: كيمياء عضوية
Year/Level: ثالثة كيمياء وكيمياء حيوية
Program Title:
  • Chemistry/Biochemistry
Specialization:
Teaching Hours: Theoretical: 4Tutorial: 1Practical: 8
2- Course aims :-
  1. •Introduce the basic information of alicyclic and polynuclear compounds
  2. •Introduce the principles of nomenclature of alicyclic and polynuclear compounds.
  3. •Study the methods of preparation of major classes of alicyclic and polynuclear compounds.
  4. •Study the physical and chemical properties of major classes of alicyclic and polynuclear compounds.
  5. •Introduce the basic information of heterocyclic compounds.
  6. •Introduce the principles of nomenclature of heterocyclic compounds.
  7. •Study the methods of preparation of major classes of heterocyclic compounds
  8. •Study the physical and chemical properties of major classes of heterocyclic compounds.
3- Course Learning Outcomes :-
4- Course contents :-
NoTopicsWeek
1Alicyclic and Polynuclear: General introduction and nomenclature.
2General methods of preparation
3General reactions (ring fission, ring contraction & ring enlargement)
4Derivatives of alicyclic compounds
5Baeyer’s strain theory -stereochemistry.
6Diphenyl- triphenyl- fused systems
7Naphthalene and its derivatives
8Anthraceneand its derivatives-phenanthrene.
9Heterocyclic:• Introduction- nomenclature- three membered rings with one and two heteroatoms.
10• Five membered rings with one and two heteroatoms or more.
11• Fused ring systems involving pyrrol- furane and thiophene (indol, benzofuran and benzothiophene).
12• Six membered rings (with one and two heteroatoms or more; pyridine, pyrylium salts, pyrans, pyrimidines, diazines, triazines, oxazines and thiazines).
13• Benzo analogues of pyridine (e.g. quinolines and isoquinolines).
14Practical: Investigation – Separation of mixtures

5- Teaching and learning methods :-
SMethod
Lectures using board
Home works, reports and discussion groups
Laboratory work

6- Teaching and learning methods of disables :-
  1. The same as normal students, only skeletal disabilities are allowed in the Faculty of Science.

7- Student assessment :-
A. Timing
NoMethodWeek
1Final exam14
2Oral exam14
3Practical exam12
4Quizzes4, 8, 12
5Report10
B. Degree
NoMethodDegree
1Mid_term examination0
2Final_term examination70
3Oral examination 10
4Practical examination 20
5Semester work0
6Other types of asessment0
Total100%

8- List of books and references
SItemType
1Course Notes:Chemistry of Alicyclic and Polynuclear Compounds
2Chemistry of Heterocyclic Compounds
3Morrison & Boyd, Organic Chemistry, Allyn & Bacon, Inc., Boston, 3rd Edn. (1973)
4Finer,L., Organic Chemistry, 5th Edn., ELBS and Longman group Ltd. (1975).
5Fessenden & Fessenden, Organic Chemistry, Willard Grant Press, Boston, Massachusetts, 2nd Edn. (1982)
6http://en.wikipedia.org/wiki/Organic_chemistry
7http://www.organic-chemistry.org/
8http://www.acdlabs.com/iupac/nomenclature/

9- Matrix of knowledge and skills of the course
SContentStudy week
Alicyclic and Polynuclear: General introduction and nomenclature.
General methods of preparation
General reactions (ring fission, ring contraction & ring enlargement)
Derivatives of alicyclic compounds
Baeyer’s strain theory -stereochemistry.
Diphenyl- triphenyl- fused systems
Naphthalene and its derivatives
Anthraceneand its derivatives-phenanthrene.
Heterocyclic:• Introduction- nomenclature- three membered rings with one and two heteroatoms.
• Five membered rings with one and two heteroatoms or more.
• Fused ring systems involving pyrrol- furane and thiophene (indol, benzofuran and benzothiophene).
• Six membered rings (with one and two heteroatoms or more; pyridine, pyrylium salts, pyrans, pyrimidines, diazines, triazines, oxazines and thiazines).
• Benzo analogues of pyridine (e.g. quinolines and isoquinolines).
Practical: Investigation – Separation of mixtures

Course Coordinator(s): -
  1. Eman Mohamed Mahmoud Hessen Keshk
Head of department: -
Awad Ebrahim Ahmed Mohamed