BSc Biomedical Sciences / Course details
Year of entry: 2022
- View tabs
- View full page
Course unit details:
Fundamentals of Chemistry
|Unit level||Level 1|
|Teaching period(s)||Semester 1|
|Available as a free choice unit?||No|
This course unit detail provides the framework for delivery in 22/23 and may be subject to change due to any additional Covid-19 impact.
This course is specifically designed for Biology students who have not taken Chemistry at A level or equivalent. It aims to provide a basic introduction to the fundamental principles and concepts of chemistry that are relevant to biologists.
CHEM10111 aims to provide a description of: atomic structure and molecular structure using various models for chemical bonding; the structure and properties of aromatic and heteroaromatic molecules; the phenomena of electron delocalisation (resonance); to explain aspects of conformation, isomerism and chirality within molecules; to provide an introduction to the thermodynamics of solutions; and to cover key concepts in chemical reaction kinetics and redox processes.
On successful completion of the course students should be able to demonstrate a working knowledge of the basic principles of physical, inorganic and organic chemistry sufficient to recognise their involvement in biological and other areas.
More specifically, students should be able to:
• State or calculate values associated with a given atom or ion (e.g. atomic / mass number, number of protons / neutrons / electrons, relative atomic mass)
• Determine the electronic configuration and draw orbital energy diagrams using Hund’s rule and the Pauli exclusion principle
• Draw and interpret Lewis structures (including formal charges) for molecules containing H, C, N and O, and predict their geometry based on VSEPR theory
• Identify characteristics of a given atom or molecule (e.g. hybridisation state, relative bond length, bond polarity, molecular dipoles, hindered bond rotation)
• Identify characteristics of biologically-important molecules (e.g. conjugation, planarity, resonance forms, aromaticity, number of pi-electrons)
• Identify chiral molecules and chiral centres of molecules with biological relevance
• Assign groups of molecules as being identical, distinct or isomeric (including constitutional, geometric and optical isomers)
• Identify simple functional groups and interconvert structures and standard names of simple, biologically-relevant molecules.
• State and calculate equilibrium constants and describe the behaviour of reversible reactions using Le Chatelier’s principle
• Calculate the pH of solutions of both strong and weak acids, and of solutions containing buffers
• Calculate the Gibbs free energy from enthalpy and entropy, and from an equilibrium constant and relate this information to the equilibrium position of a reversible reaction
• Calculate the enthalpy of combustion using Hess’s law
• Use transition state theory to relate the free energy barrier and rate of a reaction
• Determine the rate equation for a given reaction and use the concentration-dependence of an observed rate constant to determine the rate order
• Characterise biologically-important reactions as oxidation or reduction reactions and determine reduction potentials from their Nernst half-reactions
CHEM10111 is taught as six topics, or learning modules (LMs):
LM 1. Atoms, ions and molecules; the periodic table and periodicity; atomic structure; electron configurations.
LM 2. Chemical bonding and non-covalent interactions.
LM 3. Functional group recognition and reaction types.
LM 4. Stereochemistry and chirality; resonance and aromatics;
LM 5. Equilibria, pH and buffers; basic thermodynamics.
LM 6. Oxidation and reduction; reaction rates.
Transferable skills and personal qualities
Problem solving and reasoning.
Numerical skills (mathematical calculations).
- Analytical skills
- Analytical skills may be developed through problem-solving clinics and e-learning modules
- Oral communication
- Students are encouraged to ask and answer questions during lectures and workshops.
- Problem solving
- Students have the opportunity to develop their problem solving skills in problem-solving clinics workshops and eLearning modules
Feedback is via two in person workshop/problem solving clinics/revision sessions each week.
There are also regular online quizzes (ePBL tests) that provide feedback via formative (practice) tests.
There are also drop-in sessions for CHEM10111 run by PASS Leaders throughout the semester. The leaders are higher year students in the School of Biological Sciences who took CHEM units in their first year.
Bruice, PY Organic Chemistry, 6th, 7th or 8th edition, Prentice-Hall, 2011, 2014 or 2016.
|Scheduled activity hours|
|Assessment written exam||2|
|Independent study hours|
|Sam Hay||Unit coordinator|
Weighting within unit (if relevant)
LM1-LM6 ePBL blackboard tests
Exam - MCQ and multiple answer format hosted on blackboard.
6 x 10 MCQs