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Organic Chemistry - MC270P26
Title: Organická chemie (c-biol)
Guaranteed by: Department of Organic Chemistry (31-270)
Faculty: Faculty of Science
Actual: from 2013
Semester: summer
E-Credits: 3
Examination process: summer s.:
Hours per week, examination: summer s.:2/0, Ex [HT]
Capacity: unlimited
Min. number of students: unlimited
4EU+: no
Virtual mobility / capacity: no
State of the course: cancelled
Language: Czech
Note: enabled for web enrollment
Guarantor: prof. Ing. Michal Hocek, CSc., DSc.
Interchangeability : MC270P76
Opinion survey results   Examination dates   Schedule   
Annotation
Basic information: what is organic compound, isomers (constitutional, geometrical, stereoisomers, conformations), chemical bonding (single, double, triple bond, polarity, aromaticity), classification of organic compounds (hydrocarbons, derivatives - functional groups), chemical nomencalture. Overview of organic compounds: alkanes, alkenes, alkynes, arenes, halides, nitro compound, amines, alcohols, phenols, ehters, carbonyl compounds, carboxylic acids and their derivatives. Mechanisms of selected reaction types. Naturally occuring compounds.
Last update: SMRCEK (27.09.2002)
Literature - Czech

J. Svoboda: Organická chemie I.; VŠCHT Praha; http://vydavatelstvi.vscht.cz/katalog/uid_isbn-978-80-7080-561-9/anotace/

J. McMurry: Organická chemie, VŠCHT Praha; http://vydavatelstvi.vscht.cz/katalog/uid_isbn-978-80-7080-637-1/anotace/

Trnka T., Klinotová E., Kotora M., Sejbal J. Organická chemie pro posluchače nechemických oborů, PřF UK

Praha 2002

Last update: Machara Aleš, Ing., Ph.D. (03.05.2012)
Requirements to the exam - Czech

Zkouška písemná - >50% (orientační hodnocení: 50-65 dobře, 65-79 velmi dobře, >80 následuje ústní zkouška). Pro stupeň výborně je třeba úspěšně zvládnout ústní část.

Last update: Machara Aleš, Ing., Ph.D. (03.05.2012)
Syllabus -

Introduction

What is organic chemistry about

Organic chemistry and nature

Organic chemistry in everyday life

Chemical Bond

How are electrons arranged in atoms and hybridization

Covalnt bond ovalentní vazba

Inductive effect, resonance

Isomerism

Alkanes and cycloalkanes

Nomenclature of alkanes

Reactions of alkanes

Isomerism a conformation

Alkenes and alkyesy

Addition reactions

Markovnikov´s rule

1,4-Addition

Stereochemistry

Chirality, elements of symmetry

Enantiomers, biological properties

Aromatic compounds

Definition of aromaticity

Electrofilic aromatic substitution

Directing groups

Polycyclic aromatic compounds

Organic halogen compounds

Synthesis of organic halides

SN1 and SN2 substitutions

E1 and E2 mechanisms

Alkohols a fenols

Properties of alcohols (hydrogen bonding, acidity, bazicity, nucleophilicity)

Reactions of alcohols

Thiols, ethers a thioethers

Aldehydes, ketones

Carbonyl group

Synthesis of alcohols and ketones

Nucleophilic addition to C=O (alcohols, Grignard reagents, hydrides, cyanides)

Keto-enol tautomerism

Enolates, their application in synthesis (aldol condenzation, malonesterreactions)

Quinones

Carboxylic acids

Acidity (pKA), resonance structures of carboxylic anion

  • I effect

Synthesis of carboxylic acids

Esterification and esters, amides, nitriles, acylhalides

Thioesters

Amines

Synthesis of amines

Bazicity, hydrogen bonding

Reaction with acids, quaternization

Reaction with nitrous acid

Diazocoupling

Heterocyclic amines

Carbohydrates

Fischer and Haworth formulas, conformation formulas

Oxidation, reduction

Acylation, etherification

Oligosacharides, polysacharides

Aminoacids and peptides

Peptide bond

Peptide synthesis

Natural compounds

Last update: SMRCEK (20.01.2003)
 
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