KE501: Kemi 1 – Fundamental Chemistry (10 ECTS)

STADS: 10004701

Level
Bachelor course

Teaching period
The course is offered in the autumn semester.
1st and 2nd quarter.

Teacher responsible
Email: mip@ifk.sdu.dk
Email: pon@ifk.sdu.dk

Timetable
Group Type Day Time Classroom Weeks Comment
Common I Monday 12-13 U55 37-38, 40-41, 43, 45-49
Common I Wednesday 13-14 U55 37-41, 43, 45-49
Common I Thursday 12-13 U55 36, 38, 40-41, 45-49
Common I Thursday 12-14 U55 37, 39
S1 TE Monday 15-17 U49D 37-41, 43, 45-47,49-51
S1 TE Friday 08-10 U49D 36, 38, 43, 49-51
S1 TE Friday 08-10 U49d 47
S2 TE Monday 10-12 U49D 38, 43
S2 TE Monday 10-12 Kollokvierummet 39
S2 TE Wednesday 10-12 U49D 37-41, 43, 45-51
S2 TE Friday 12-14 U49D 49-51
S3 TE Wednesday 08-10 U49D 37-41, 43, 45-51
S3 TE Friday 08-10 U14 36, 38, 43, 49-51
S4 TE Tuesday 08-10 U49c 38, 43, 51
S4 TE Tuesday 08-10 U131 39
S4 TE Thursday 10-12 U49D 37-41, 43, 45-51
S4 TE Friday 08-10 U69 48,51
S5 TE Tuesday 14-16 U49D 37-41, 43, 45-51
S5 TE Wednesday 10-12 U49c 51
S5 TE Thursday 08-10 U49c 37
S5 TE Thursday 08-10 U49D 38, 43, 51
S5 TE Thursday 13-15 U103 48
S6 TE Monday 08-10 U73 37-41,43,45-51
S6 TE Thursday 14-16 U7 36,38,43,49-51
S12 TE Wednesday 14-16 U49D 37-41, 43, 45-51
S12 TE Friday 08-10 U49d 37
S12 TE Friday 08-10 U17 38
S12 TE Friday 12-14 U49D 43
S12 TE Friday 10-12 U49D 49-51
S13 TE Monday 12-14 U49d 39
S13 TE Tuesday 08-10 U92 38,43,49-51
S13 TE Wednesday 08-10 U66 37-41
S13 TE Friday 10-12 U74 43
S13 TE Friday 10-12 U49b 45-51
S81 TE Monday 08-10 U49D 38, 40, 43, 49-51
S81 TE Monday 08-10 U49d 39
S81 TE Friday 14-16 U49D 37-39, 41, 43, 45-51
S82 TE Monday 10-12 U14 37-38,40-41
S82 TE Monday 14-16 U57 43,45
S82 TE Tuesday 14-16 U7 39,43
S82 TE Tuesday 14-16 U143 46-51
S82 TE Wednesday 08-10 U49c 37
S82 TE Wednesday 08-10 U57 38
S82 TE Thursday 12-14 U59 50-51
S82 TE Friday 08-10 U35 49
T1 TE Monday 13-15 IFK 37-41, 43, 45-51
T1 TE Thursday 14-16 IFK 36, 38, 43, 49-51
Show entire timetable
Show personal time table for this course.

Revison of timetable:
: Skemaændringer i uge 37 og 39.

Prerequisites:
None

Academic preconditions:
None.

Course introduction
The aim of the course is to provide the students with knowledge of chemistry at such a level that the acquired knowledge can form the background of advanced studies within chemistry and support related disciplines, e.g. biology, biochemistry, biotechnology, bioinformatics, biomedicine, physics and chemical engineering.

Expected learning outcome
For the examination, the students are expected to be able to:
- describe the connection between quantum numbers and orbitals
- explain the significance of different types of chemical bonding and recognize the concept of hybridisation
- relate knowledge on chemical bonding, orbitals and hybridization to problems in general chemistry
- draw Lewis-structures for simple molecules and ions and argue for their geometry using the VSEPR-model
- recognize the concept of resonanse in the context of simple inorganic molecules and ions
- employ Le Chatelier’s principle on chemical equilibria and perform calculations on equilibrium mixtures from equilibrium constants
- explain the concept of intermolecular interactions
- determine concentrations from titrations and eqilibrium constants and relate pH-calculations to the titration curves for acid/base titrations
- recognize reaction types of zero, first and second order, employ integrated reaction rate equations, Arrhenius' equation and recognize catalysis and molecularity
- determine reaction order, half lives and activation energies from experimental data
- recognize and employ the concepts of enthalpy, entropy, heat capacity, free energy and solubility constant in simple calculations
- recognize and employ the fundamental concepts of Galvanic and electrolytic cells, Faraday’s law and Nernst’s equation
- perform calculations of concentrations, potentials and equilibrium constants
- read and draw organic chemical structures and formula
- recognize the basic structures and the functional groups and to assess the relevance of these for the properties of concrete compounds including polarity, reactivity in aqueous solutions and the possibility for intermolecular bonds.
- explain the most common reactions for different organic classes of compounds based on basic structures and functional groups including saturated and unsaturated carbonhydrids, aromatic compounds, halogencompounds, alcohols, ethers, amines and carbonylcompounds.
- employ the nomenclature for simple organic molecules and recognize the most common trivial names
- employ the basic concepts for stereochemistry and isomeri as well as the concepts configuration and conformation
- employ simple mechanisms in the explanation of the most common reactions
- explain the most important aspects of nucleophilic substitution, electrophilic addition and elimination.
- explain the most important aspects of elektrophilic aromatic substitution and emply the concept of resonance in accordance to organic molecules
- explain the use of condensation, hydrolysis, oxidation and reduction.
- describe and suggest simple organic syntheses from a judgement of basic structures and functional groups as well as the reactivity of these
- relate chemical reactivity to practical experiment


Subject overview
  • Atomic structure related to the construction of the periodic table
  • Concepts concerning the chemical bonding, includingCovalent and non-covalent bonding
  • Molecular structure, including Aliphatic and aromatic hydrocarbons and alkyl halides, Functional groups, stereochemistry and nomenclature
  • Chemical equilibrium, including Acids and bases, buffers and ampholytes Solubility product and heterogeneous equilibria
  • Thermodynamics, including The first law of thermodynamics, energy and enthalpy, The second law of thermodynamics, entropy and free energy, Electrochemistry
  • Reaction kinetics
  • Organic chemical reactions, including The concept of resonance and reaction mechanisms, Alcohols, phenols and ethers, aldehydes and ketones, Carboxylic acids, carboxylic acid derivatives and amines, Keto-enol tautomerism, Elimination, Nucleophilic substitution, Electrophilic aromatic substitution
Literature
  • Blackman et al.: Chemistry, Wiley 2008.


Syllabus
See syllabus.

Website
This course uses e-learn (blackboard).

Prerequisites for participating in the exam
None

Assessment and marking:
4 hour written exam after the 2nd quarter with all aids allowed. The exam incorporates elements from KE501A and KE501S. External marking and grade according to 7-scale.

Re-examination after 4th quarter.

Expected working hours
The teaching method is based on three phase model.

Forelæsninger (34 t), eksaminatorier og opgaveregning (38 t).
Educational activities

Language
This course is taught in Danish.

Remarks
The 10 ECTS includes following two 1 ECTS elements: KE501A and KE501S

Course enrollment
See deadline of enrolment.

Tuition fees for single courses
See fees for single courses.