PH1S085 - Organic Molecules: their Structure, Reactivity and Analysis 01 Aug 2023 - 31 Aug 2029 | Version 1
Associated Module Information
| Module Code: | PH1S085 | ||
|---|---|---|---|
| Module Title: | Organic Molecules: their Structure, Reactivity and Analysis | ||
| Faculty: | Faculty of Computing, Engineering and Science | ||
| Faculty Group: | Applied Sciences | ||
| Faculty Sub Group: | Chemistry and Pharmaceutical Science | ||
| Module Leader: | Suzanna Kean | ||
| Module Team: | Andrew Graham, Rehana Karim | ||
| First Intended Intake: | SEP 2028 | Final Year of Intake: | 2028 |
| Date Closed: | |||
| Credit Value: | 20 | Credit Level: | 4 |
| Language: | English | ||
| Percentage of Module Taught in Welsh: | 0 | ||
| Equivalent Module: | |||
| HECOS codes: | 100413 - analytical chemistry | 100422 - organic chemistry | |
| HECOS Code Weighting: | 20 | 80 | |
Document Version Information
| Version | 1 |
|---|---|
| Valid From | 01 Aug 2023 |
| Valid To | 31 Aug 2029 |
Module Aims
1. To introduce the scope and special features of fundamental organic chemistry.
2. To introduce techniques of organic/spectroscopic analysis and apply relevant data to problem solving in organic chemistry
3. To illustrate concepts in the laboratory and to impart relevant practical skills
Content Summary
This module is designed to develop and support the students application of fundamental concepts in the areas of organic and analytical chemistry. Students will study the following:
1) Understanding organic molecules:
Recognising bonding within organic molecules (valency, hybridization, bonding orbital theory (sigma/pi bonds))
Using names and drawing structures to communicate about molecules (functional group recognition, concept of homologous series, nomenclature of organic compounds, drawing/representing organic compounds: molecular formula, condensed formula, full displayed structural formula, line diagrams).
The complexity of organic structures (structural isomers: positional, functional group and chain isomers. Stereoisomers: geometric and optical isomers (assigning/naming both E/Z and cis/trans for geometric isomers and R/S for optical isomers up to two chiral centres), their properties, how to draw, concept of diastereomers and meso compounds. Conformers of alkanes: importance in some reactions, Newman projects of different conformers, concept of steric hinderance).
How do organic molecules react/interact (Intermolecular forces: types and how they govern the physical properties of organic compounds. Fundamental reactions in organic chemistry: bond polarity, bond breakage/formation (homolysis, heterolysis), type of reagents (electrophiles/nucleophiles/radical), types of reactions (addition/elimination/substitution/rearrangement). Fundamental mechanisms in organic chemistry: non-polar (radical addition/substitution, chain reactions, the stability of radical species), polar (electrophilic addition reactions: importance of stability of carbocations in determining product, Markovnikov’s rule; SN1/SN2: factors affecting, e.g., solvent nucleophile, leaving group, steric factors; E1/E2: factors that govern choice of).
2) Organic Transformations
The properties and reactions of some fundamental organic compounds including characteristic chemical tests for: the alkanes, alkenes, halogenoalkanes and alcohols, an introduction to the carbonyl containing compounds (aldehydes/ketones/carboxylic acids/carboxylic acid derivatives) and the amines, nitriles and amides. Multistep reactions that interconvert between these functional groups.
Aromatic compounds: The special case of benzene, conjugation and resonance, introduction to aromaticity (Huckels rule), naming benzene compounds, electrophillic aromatic substitution reactions, substituent effects (directing/activating effects of electron withdrawing or electron donating groups), nucleophilic aromatic substitution, specific aromatic compounds and their reactions: halogenated aromatic compounds, phenols, phenyl amine, akylbenzenes
3) Fundamental Organic Analysis
Elemental analysis, determination of double bond equivalency, UV-Vis spectroscopy (basic principles and interpretation of spectra), IR analysis (basic principles and interpretation of spectra primarily to identify characteristic functional groups), 1H and 13C NMR (basic principles and interpretation of spectra (number of signals/chemical shift/integration/splitting patterns) to elucidate full structures), mass spectrometry (basic principles and interpretation of spectra primarily for mass determination and fragment identification, introduction to concept of rearrangements of fragments). Multispectral analysis.
4) Fundamental laboratory skills
Extraction techniques e.g., liquid/liquid extraction, chromatography (e.g., thin layer chromatography), purification techniques e.g., recrystallisation, methods of analysis (e.g., chromatography, melting points), relevant data analysis and calculations. Safe laboratory practices.
Learning and Teaching Methods
| Activity Type | Hours |
|---|---|
| Lecture | 18 |
| Practical classes and workshops | 12 |
| Independent Study | 50 |
| Directed Study | 102 |
| Problem / challenge based learning | 18 |
| Total Hours Selected | 200 |
Learning Outcomes
| # | Learning Outcome |
|---|---|
| LO1 | Acquire and apply the basic concepts that underpin organic chemistry including structures, shapes, physical interactions, reaction mechanisms, and analysis. |
| LO2 | Evaluate scientific data and develop practical skills to solve problems. |
Assessment Criteria
| Assessment Category | Assessment Type | Description | Duration | Word Count | Weight (%) | Best of? | Pass Mark |
|---|---|---|---|---|---|---|---|
| Synchronous Onsite Practical Assessment | Practical Coursework (Onsite) 1 | A series of guided assessments demonstrating the application of practical skills and problem solving | 0 | 2000 | 50 | No | 40 |
| Asynchronous Assessment | Report 1 | Written assignment allowing demonstration of the taught theory of the module. | 0 | N/A | 50 | No | 40 |
Assessment Matrix
| Assessment Type | Learning Outcomes | ||
|---|---|---|---|
| LO1 | LO2 | ||
| Practical Coursework (Onsite) 1 | ✔ | ✔ | |
| Report 1 | ✔ | ✔ | |