Degree | Type | Year | Semester |
---|---|---|---|
2501922 Nanoscience and Nanotechnology | OB | 2 | 1 |
It is appropriate to have approved the subjects “Reactivitat Química” and "Enllaç Químic i Estructura de la Matèria”.
Organic Chemistry studies the reactivity of carbon and systematizes the properties of the compounds that contain it. Basic ideas about the characteristics and reactivity of the different functional groups are given, as well as the conformational analysis and the stereochemistry of organic compounds.
The objectives are:
1. Identify the functional groups and name and formulate the corresponding compounds.
2. Draw Lewis structures of organic chemical compounds and qualitatively predict their molecular properties from them (molecular geometry and polarity).
3. Describe the conformational isomerism in alkanes and cycloalkanes.
4. Determine and represent the configuration of the stereogenic centers in organic compounds.
5. Describe the basics of organic reactions.
6. Resolve basic problems of organic chemistry.
1. Introduction (Lewis structures, resonance, coordinates and reaction profile).
2. Alcans (Constitutional isomerism, optical isomerism, enantiomers, diastereoisomers).
3. Halogenated derivatives (Structure and obtaining, nucleophilic substitution, reactions SN1 and SN2, eliminations).
4. Alkene and alkynes (Bond, isomers, properties, reactions, additions, oxidations).
5. Alcohols and ethers (Alcohols: structure and properties, obtaining and reactions, oxidation of alcohols, ethers: properties, synthesis, epoxides).
6. Aldehydes and ketones (The carbonyl group: structure and properties, obtaining aldehydes and ketones, reactions of oxidation, reduction and addition, keto-enol tautomerism).
7. Carboxylic acids and derivatives (Electronic structure, acidic character, physical properties, obtaining, derivatives, esters, lactones).
8. Nitrogen derivatives (Amines, properties, obtaining, ammonium salts).
9. Diens, polyens and benzene (Electronic structure, benzene-aromaticity, aromatic hydrocarbons, aromatic electrophilic substitution).
10. Benzene derivatives (Ring reactions, effect of substituents, nitrogen derivatives, phenols).
11. Polymers (Characteristics, obtaining, most important polymers, structure and properties).
Theory classes
The student acquires the own knowledge of the subject attending the classes of theory that will complement with the individualized study.
Problems classes
The student consolidates the knowledge acquired in theory classes by solving problems. A dossier of exercises will be delivered that will have to be resolved throughout the course. A selected part of these exercises will be solved by problem teachers so that students learn the appropriate methodology to find the solutions. During this process, students' participation will be important. Teachers will help to develop the critical sense and logical reasoning, in order to increase the ability of students to solve problems.
Classes of Practices
The laboratory classes focus on the learning of the basic techniques and to familiarize the student with the conditions of security that manipulation of chemical products requires. In order to be able to attend the sessions of laboratory practices, the student must justify having passed the security tests that will be found in the Virtual Campus and be aware of, and accept, the rules of operation of the laboratories of the Faculty.
Annotation: Within the schedule set by the centre or degree programme, 15 minutes of one class will be reserved for students to evaluate their lecturers and their courses or modules through questionnaires.
Title | Hours | ECTS | Learning Outcomes |
---|---|---|---|
Type: Directed | |||
Laboratory practices | 16 | 0.64 | 1, 2, 22, 9, 5, 11, 13, 15, 12, 26, 27, 16, 24, 17, 18, 19, 20, 40, 6, 7, 39, 4, 41, 25, 28, 29, 30, 31, 32, 34, 35, 33, 14, 36, 37, 38, 47, 8, 23, 42, 43, 46, 45, 44 |
Problems | 12 | 0.48 | 22, 5, 10, 11, 13, 15, 24, 18, 19, 4, 41, 25, 28, 29, 30, 31, 32, 34, 35, 14, 38, 47, 45 |
Theory | 26 | 1.04 | 1, 2, 22, 9, 5, 10, 11, 13, 15, 12, 24, 18, 19, 4, 41, 25, 28, 29, 30, 31, 32, 34, 35, 33, 14, 38, 47 |
Type: Supervised | |||
Tutorials | 4 | 0.16 | |
Type: Autonomous | |||
Homework | 7.5 | 0.3 | 22, 10, 13, 16, 24, 32, 45, 44 |
Laboratory practices | 3.5 | 0.14 | 1, 2, 22, 9, 5, 12, 26, 27, 16, 24, 17, 18, 19, 20, 40, 6, 7, 39, 4, 41, 25, 29, 32, 35, 33, 14, 36, 37, 38, 47, 8, 23, 42, 43, 46, 45, 44 |
Problems | 13.5 | 0.54 | 1, 22, 5, 10, 11, 13, 15, 24, 18, 4, 41, 25, 28, 29, 30, 31, 32, 34, 35, 33, 38, 47, 45, 44 |
Theory | 56.5 | 2.26 | 2, 22, 5, 10, 11, 13, 15, 24, 18, 19, 4, 25, 28, 30, 31, 32, 34, 35, 14, 38, 47 |
A continuous evaluation of the competences will be carried out that will include a work and written tests.
The system is organized in 3 modules, each of which will have a specific weight assigned to the final grade:
- Written work module: Assess the learning and use of a free molecular naming and drawing program with individual work. This module will have a global weight of 10%.
- Laboratory module: the student's performance in the laboratory will be evaluated and an examination with a global weight of 20% will be performed.
- Module of partial written tests: it will consist of two partial tests with a weight of 30% the first one, and 40% the second.
In order to pass the subject, you must draw at least 4 points out of 10 in each of the two written partial tests and the writen work and laboratory practices must be done and approved. The subject will be considered to be exceeded when the average of the modules is equal to or greater than 5 points out of 10.
- Students who do not pass the first and / or the second partial exam may take a recovery test after the second partial exam. In order to do this recovery, the student is obligated to submit to both partial examinations.
- The students who finally do not obtain the minimum qualification required to be able to pass each one of the tests of the partial written test module or the minimum qualification to be able to pass the module of written work or the module of Laboratory, will not approve the subject. In this case, the final maximum grade will be 4.
-From the second enrollment of the subject it will not be necessary for the student to complete the written work module or the laboratory module if he has achieved the competences of this part of the subject in the previous year. A student will obtain the non-appraising (No Avaluable) qualification when the number of assessment activities carried out is less than 50% of those programmed for the subject (work, both exams and four practical sessions).
Title | Weighting | Hours | ECTS | Learning Outcomes |
---|---|---|---|---|
Laboratory module | 20% | 4 | 0.16 | 1, 2, 22, 9, 5, 11, 13, 15, 12, 26, 27, 16, 17, 18, 19, 21, 20, 40, 6, 7, 39, 4, 41, 28, 29, 30, 31, 32, 34, 35, 33, 14, 36, 37, 38, 8, 23, 42, 43, 46, 45, 44, 3 |
Module of partial written tests and examination of recovery | 40% (first writen test) + 30% (second writen test) | 6 | 0.24 | 2, 9, 10, 11, 13, 15, 18, 19, 20, 4, 41, 28, 29, 30, 31, 32, 34, 35, 38 |
Work of molecular naming and drawing | 10% | 1 | 0.04 | 22, 5, 10, 13, 24, 18, 4, 25, 29, 32, 35, 38, 47, 45 |
1.- i) Bruice, P.Y. Organic Chemistry, 8th Ed. Ed. Pearson Education, 2017 (ISBN 9781292160344, ISBN1292160349 ).
ii) Bruice, P.Y. Essential Organic Chemistry, 3rd Ed. Ed. Pearson Education, 2016 (ISBN 9781292089034).
iii) Bruice, P. Y. Química Orgánica, 5ª Edición, Ed. Pearson Educación, México, 2008 (ISBN 9789702607915).
2.- Solomons T.W.G. Química Orgánica, 3ª Ed. Ed. Limusa S.A. 2014 (Vol. 1: ISBN 10 9786070506963, Vol 2: 9786070506970).
3.- Carey F.A., Giuliano R.M. Química Orgánica, 9a Ed. Ed. McGraw-Hill, 2014 (ISBN 9786071512109).
4- IUPAC Nomenclatureof Organic Chemistry:
i) https://iupac.qmul.ac.uk/BlueBook/
ii) https://publicacions.iec.cat/repository/pdf/00000195/00000013.pdf
iii) https://www.upo.es/depa/webdex/quimfis/docencia/quimbiotec/Nomenclatura_organica.pdf
5.- ACD/ChemSketch for Academic and Personal Use. A Free Comprehensive Chemical Drawing Package: http://www.freechemsketch.com
6.- Pulido F. Nomenclatura de Química Orgánica: http://es.slideshare.net/manoa21/nomenclatura-quimicaorganica-29646851?next_slideshow=1
7.- Rosso V. Química Orgánica Nomenclatura: http://es.slideshare.net/verorosso/qumica-orgnica-nomenclatura?qid=09239331-ba5c-4096-9104-dd4cb26fe630&v=qf1&b=&from_search=3
The course material will be found in the space of the subject of the Virtual Campus of the UAB. Among this material you will find: general information, marks of the final exam and any other information that is considered of interest to the students.
ACD/ChemSketch for Academic and Personal Use. A Free Comprehensive Chemical Drawing Package: http://www.freechemsketch.com