617-0810/01 – Organic Chemistry (OCH)

Gurantor departmentDepartment of ChemistryCredits5
Subject guarantordoc. Ing. Petr Pánek, CSc.Subject version guarantordoc. Ing. Petr Pánek, CSc.
Study levelundergraduate or graduateRequirementCompulsory
Year1Semesterwinter
Study languageCzech
Year of introduction2005/2006Year of cancellation2015/2016
Intended for the facultiesFMTIntended for study typesFollow-up Master
Instruction secured by
LoginNameTuitorTeacher giving lectures
KUL37 doc. Ing. Lenka Kulhánková, Ph.D.
PAN37 doc. Ing. Petr Pánek, CSc.
Extent of instruction for forms of study
Form of studyWay of compl.Extent
Full-time Credit and Examination 3+2

Subject aims expressed by acquired skills and competences

Repeticion of theoretical principles of the organic chemistry and extension of the knowledge about the most important groups of organic substances from the technical and biological point of view.

Teaching methods

Lectures
Tutorials
Experimental work in labs

Summary

The review of the key principles of the organic chemistry, modern methods of organic synthesis and organic analysis, as well as extension of the knowledge about the most important groups of organic compounds.

Compulsory literature:

1) Solomons, T.W.G.,Fryhle C.B: Organic Chemistry. John Wiley & Sons,Inc. 2003 ISBN 0-471-41799-8

Recommended literature:

1) John McMurry Organic chemistry . - 6th ed.. - Belmont : Thomson Brooks/Cole, 2004. pp. 1176, ISBN 0-534-38999-6 2) W. H. Brown: Organic Chemistry (Saunders College Publishing, 1995) 3) W. H. Brown: Organic Polymer Chemistry: (Saunders College Publishing, 1995)

Way of continuous check of knowledge in the course of semester

E-learning

Další požadavky na studenta

There are no additional requirements for students.

Prerequisities

Subject has no prerequisities.

Co-requisities

Subject has no co-requisities.

Subject syllabus:

1. Lecture: Introduction into the organic chemistry. History of organic chemistry. Bonding power of carbon (molecular orbitals,  and  bond, energy of bond, polarity of bond, hybridization, effects of electron). Relation between the structure and the properties of substances. Intermolecular interaction (Van der Waals interaction, interaction of dipole, hydrogen bridges) and their influence on the temperature of the reversion (thaw point, boiling point) and solubility. Theoretical tutorial: Bonding power of carbon. 2. Lecture: Principles of stereochemistry of organic compounds. Drawing organic molecules (types of formulas, projection, models, 3D-shape of molecules). Polymerism and isomerism (constitution, geometric, enantiomerism). The conformation of organic compounds. Theoretical tutorial: Structure, formula, model. Inference of molecular formula, rational formula and structural formula. Determination of isomerism type by the concrete compounds. 3. Lecture: Chemical reactions of organic compounds. Ranking of organic reactions. Homolysis and heterolysis. Electrophilic and nucleophilic agents. Aliphatic and alicyclic hydrocarbons. Nomenclature of saturated hydrocarbons. Radical substitution. Cracking (catalyzed and uncatalyzed) and isomerization. Fischer-Tropsch synthesis. Resources of hydrocarbons and their application. Theoretical tutorial: Nomenclature of organic compounds. 4. Lecture: Unsaturated hydrocarbons. Radical and ion addition to double bond. Elimination reactions. Resources of unsaturated hydrocarbons and their industrial application. Theoretical tutorial: Nomenclature of organic compounds. 5. Lecture: Aromatic compounds. Delocalization of  electrons. Electrophilic aromatic substitution (nitration, sulfonation, alcylation, acylation, halogenation) and others reactions. Resources of aromates and their industrial application. Toxicity of polyaromatic compounds. Theoretical tutorial: Nomenclature of organic compounds. 6. Lecture: Derivatives of hydrocarbons. Derivatives of halogens. Physical properties, toxicity and application. Synthesis and important reactions. Theoretical tutorial: Nomenclature of organic compounds. 7. Lecture: Derivatives of nitrogen (nitrocompounds, amines, diazonium salts, azocompounds). Physical properties, toxicity and application. Synthesis and important reactions. Practical tutorial: Preparing of jodoform. 8. Lecture: Derivatives of sulfure (thioalcohols and thiophenols, sulphides, sulfonic acids). Physical properties and application. Synthesis and important reactions. Detergents. Practical tutorial: Preparing of 4-nitroaniline. 9. Lecture: Derivatives of oxygen. Alcohols and phenols. Ethers. Physical properties, toxicity and application. Synthesis and important reactions. Practical tutorial: Preparing of fumaric acid. 10. Lecture: Carbonyl compounds (aldehydes and ketones). Physical properties, toxicity and application. Synthesis and important reactions. Organometallics. Reactivity, toxicity and application. Grignard reagents and their reactions. Practical tutorial: Preparing of acetylsalicyclic acid. 11. Lecture: Carboxylic acids. Physical properties and application. Synthesis and important reactions (acidity versus structure, neutralization, esterification, decarboxylation). Practical tutorial: Preparing of ethyl formate. 12. Lecture: Carboxylic acids derivatives. Halogenkyseliny. Hydroxykyseliny. Oxo carboxylic acids. Amino-acids. Physical properties and application. Synthesis and important reactions. Practical tutorial: Preparing of soda soap. 13. Lecture: Functional derivatives of carboxylic acids. Acyl halides. Anhydrides. Esters. Amides. Nitriles. Physical properties, toxicity and application. Synthesis and important reactions. Derivatives of carbonic acid (phosgene, urea and their sulfure analogues). Theoretical tutorial: More important reactions of hydrocarbons and derivatives of hydrocarbons. 14. Lecture: Polymers (divided, structure, properties, basic reactions of polymers preparing, summary of more important technical polymers). Theoretical tutorial: Presentation of seminar papers.

Conditions for subject completion

Full-time form (validity from: 2011/2012 Winter semester, validity until: 2015/2016 Summer semester)
Task nameType of taskMax. number of points
(act. for subtasks)
Min. number of points
Exercises evaluation and Examination Credit and Examination 100 (100) 51
        Exercises evaluation Credit 30  16
        Examination Examination 70  35
Mandatory attendence parzicipation:

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Occurrence in study plans

Academic yearProgrammeField of studySpec.FormStudy language Tut. centreYearWSType of duty
2015/2016 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2014/2015 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2013/2014 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2012/2013 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2011/2012 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2010/2011 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2009/2010 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2008/2009 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan
2007/2008 (N3923) Materials Engineering (3911T033) Material Recycling P Czech Ostrava 1 Compulsory study plan

Occurrence in special blocks

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