Survey
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project
Course Specifications Valid as from the academic year 2017-2018 Organic Chemistry II (I620002) Course size Credits 6.0 (nominal values; actual values may depend on programme) Study time 180 h Contact hrs 60.0 h Course offerings and teaching methods in academic year 2017-2018 A (semester 2) lecture 24.0 h seminar: coached exercises 12.0 h practicum 24.0 h Lecturers in academic year 2017-2018 Wille, Christophe LA16 lecturer-in-charge Offered in the following programmes in 2017-2018 crdts Bachelor of Science in Bioindustrial Sciences 6 Bachelor of Science in Chemical Engineering Technology 6 Bachelor of Science in Environmental Engineering Technology 6 Preparatory Course Master of Science in Biochemical Engineering 6 Technology Preparatory Course Master of Science in Chemical Engineering 6 Technology Preparatory Course Master of Science in Environmental Engineering 6 Technology offering A A A A A A Teaching languages Dutch Keywords functional groups, organic compounds, reactivity, synthesis and reaction mechanisms Position of the course This course builds on the course organic chemistry I and will continue to introduce the student to some basic concepts of organic chemistry, as well as a number of functional groups in detail. Contents Theory Study of organic compounds according to functional groups: structure, nomenclature, basic syntheses, physical properties, chemical reactions, and applications of aldehydes and ketones, carboxylic acids and functional derivatives of carboxylic acids, amines, diazonium salts, phenols, sulfonic acids and its derivatives, heterocyclic compounds and natural products Exercises Training sessions about the studied groups of components Practical part: 1 Testing for functional groups 2 Synthesis of various organic compounds 3 Extraction from organic material. The practical sessions focus on the synthesis and isolation of organic substances and on the application of the technology involved (extraction, distillation, recrystallization). There are also different identification methods for organic substances: mp, functional group tests, TLC, IR. Initial competences (Proposal) 1 The course builds on certain competences of the following courses: General Chemistry, Applied Chemistry and Organic chemistry I Final competences 1 The student has a basic understanding of structure, nomenclature, principles of 1 synthesis, physical properties, chemical reactions, occurrence and uses of some 1 important classes of organic compounds (alcohols, aldehydes and ketones, 1 carboxylic acids and functional derivatives of carboxylic acids, amines, diazonium 1 salts, phenols, sulfonic acids and derivatives, heterocyclic compounds and natural 1 products. The student can develop a detailed reaction scheme. 2 The student can develop a detailed reaction scheme. 3 The student is capable to write a scientific lab report concerning the lab experiment Conditions for credit contract Access to this course unit via a credit contract is determined after successful competences assessment Conditions for exam contract This course unit cannot be taken via an exam contract Teaching methods Lecture, practicum, seminar: coached exercises Learning materials and price 1 Slides-Christophe Wille 2 Bruice organic chemistry , Pearson (80 euro, can also be used in organic chemistry 1 II) global ed. ISBN 9781292160344 3 lab course only available in the course center(can also be used for organic chemistry 1 II) References 1 L.M. Harwood& J.C.Moody (1989). Experimental Organic Chemistry. Blackwell 1 Scientific publications Oxford – London. 2 R.Morrisson & R.Boyd (1992). Organic Chemistry, 6th ed. Prentice Hall, 1 Englewood Cliffs, New Jersey 3 Fessenden, R & Fessenden, J (1995). Organic Chemistry, Fifth Edition, Brooks/Cole, 1 California 4 A.I. Vogel, A.R. Tatchell, B.S. Furnis, A.J. Hannaford, P.W.G. Smith (1996). 1 Vogels’s Textbook of Practical Organic Chemistry, 5th ed. John Wiley & Sons, Inc., 1 New York Course content-related study coaching Questions during and after class. Lecturer availability for questions and additional explanations regarding theory and practice after appointment Evaluation methods end-of-term evaluation and continuous assessment Examination methods in case of periodic evaluation during the first examination period Written examination, oral examination Examination methods in case of periodic evaluation during the second examination period Written examination, oral examination Examination methods in case of permanent evaluation Job performance assessment, report Possibilities of retake in case of permanent evaluation examination during the second examination period is possible in modified form Extra information on the examination methods PE1 and PE2 consist of a number of questions which can be prepared on paper. During the oral exam, the answers are controlled and there could besome additional questions asked. Calculation of the examination mark First examination period: 2/3 of the points are on the written exam (theory + exercises) and 1/3 of the points are on the non-periodical evaluation (lab + report) (Proposal) 2 Second examination period: 2/3 of the points are on the written exam (theory + exercises), 1/6 of the points from the first examination period of the non-periodical evaluation (lab + report) and 1/6 on alternative laboratory assignement General rule: if a student is three times unlawfully absent from a practicum session , then (s)he gets a score ABSENT for the complete course. In order to pass the course, at least 8/20 must be achieved for both periodic evaluation (PE) and non-periodic evaluation (NPE) .If this condition is not fulfilled there is a deviation from the calculated figure if this is 10 or more : - the student achieves no less than 8/20 for both PE and NPE , then the final score becomes 9/20 - the student achieves less than 8/20 for either PE or NPE , then the final score is the lowest figure of PE or NPE (Proposal) 3