ORGANIC SYNTHESIS AND SPECTROSCOPY - 2021/2
Module code: CHE3061
In light of the Covid-19 pandemic the University has revised its courses to incorporate the ‘Hybrid Learning Experience’ in a departure from previous academic years and previously published information. The University has changed the delivery (and in some cases the content) of its programmes. Further information on the general principles of hybrid learning can be found at: Hybrid learning experience | University of Surrey.
We have updated key module information regarding the pattern of assessment and overall student workload to inform student module choices. We are currently working on bringing remaining published information up to date to reflect current practice during the academic year 2021/22.
This means that some information within the programme and module catalogue will be subject to change. Current students are invited to contact their Programme Leader or Academic Hive with any questions relating to the information available.
This is a high level module in organic chemistry, moving from the predominantly functional group approach of Level 4 beyond the skeletal construction approach of Level 5, to deal with modern and more conceptually challenging reactions and strategies for dealing with multistep syntheses. These are the reactions that are commonly used in contemporary organic synthetic chemistry.
MULHOLLAND Dulcie (Chemistry)
Number of Credits: 15
ECTS Credits: 7.5
Framework: FHEQ Level 6
Module cap (Maximum number of students): N/A
Overall student workload
Workshop Hours: 9
Independent Learning Hours: 107
Lecture Hours: 5
Tutorial Hours: 2
Guided Learning: 10
Captured Content: 17
Prerequisites / Co-requisites
Indicative content includes:
• Revision of organic reactions: Revision of mechanisms
• Retrosynthetic Analysis: Terms, definitions and basic concepts; retrosynthetic analysis: aromatic compounds; retrosynthetic Analysis: alcohols and carbonyl compounds; retrosynthetic analysis: 1,2, 1,3, 1,4 and 1,5dicarbonyl compounds; -unsaturated and 1,3dihydroxy compounds; retrosynthetic analysis: carbocyclic and heterocyclic; compounds
• Modern reactions: Polar reactions in synthesis, radical reactions in synthesis, pericyclic reactions in synthesis, asymmetric synthesis – an introduction
• Catalytic reactions in organic chemistry: Concept of catalysis. Mechanistic implications: creating a catalytic cycle. Reactions using metal catalysis; palladium-catalysed cross-coupling reactions: Heck, Sonogashira, Stille and Suzuki reactions; Pauson-Khand reaction. Small organic molecules as catalysts: BaylisHillman reaction; olefin metathesis
•Multicomponent reactions: Solid-phase synthesis and combinatorial chemistry
• Spectroscopy: Workshop 1: Introductory revision problems using 1D NMR (1H, 13C), MS, IR, UV. Use of the coupling constant, Karplus equation, coupling in aromatic systems and long range coupling; Workshop 2: Use of COSY, HSQC, DEPT, HMBC and NOESY spectra in structure determination with worked examples; Workshops 3 & 4: Structural determination of compounds using natural products and synthetic compounds (terpenoids; oxygen heterocyclics (chalcones, flavonoids); alkaloids) as examples
|Assessment type||Unit of assessment||Weighting|
|Online Scheduled Summative Class Test||In Class Test (Spectroscopy)||20|
|Examination Online||Online Open Book Exam||80|
The assessment strategy is designed to provide students with the opportunity to demonstrate:
• Examination and coursework: Assimilation of knowledge and its application to problems in modern organic chemistry [LOs 1-6]
• In-class test/assessed workshop on spectroscopy: Ability to assign structure based on spectra [LOs 4]
Thus, the summative assessment for this module consists of:
• Coursework: Problem solving on aspects of the course (15%, 18 h over 8 weeks) [LOs assessed 1-3, 5]
• In-class test/assessed workshop on spectroscopy: (15%, 2 h ICT) [LOs 4]
• Examination: 1.5 hours, closed book (70%) [LOs assessed 1-5]
Formal formative assessment is mainly in the spectroscopy workshops. There is also formative assessment in example problems posted to SurreyLearn for students to attempt and receive written or verbal feedback; also students can opt for informal formative assessment (submission of specimen exams, past papers, etc.) which will be marked and annotated. Feedback: Feedback is provided optionally on the formative practice problems. Coursework is marked and returned with feedback in time for the revision period.
- provide students with the appropriate advanced material in organic chemistry to allow them to describe and methodically rationalize a representative range of standard modern reactions/syntheses
- provide students with the skills to identify organic compounds by spectroscopy
|001||Demonstrate a conceptual understanding of modern advanced organic reactions (including their scope), including abstract concepts (combinatorial)||K|
|002||Explain chemo‐, regio‐ and stereo‐selectivity where observed in given reactions||CK|
|003||Analyse a chemical structure in terms of the retrosynthetic approach to its multistep synthesis||CK|
|004||Solve problems of structure using a range of spectroscopic techniques, particularly NMR (K, C, P – spectroscopy and practical work tend to be intertwined in organic chemistry)||CKP|
|005||Show critical evaluation of different approaches to specific problems in synthesis||C|
|006||Reviewing, assess and demonstrate critical thinking||T|
C - Cognitive/analytical
K - Subject knowledge
T - Transferable skills
P - Professional/Practical skills
Methods of Teaching / Learning
The learning and teaching strategy is designed to:
give the student a good high level knowledge base, but also but the analytical and problem-solving skills to solve unseen (but related), and to attempt some new concepts; all within the context of current practice in organic synthesis.
The learning and teaching methods include:
• Lectures 20, plus two revision lectures = 22 L
• Problem-solving coursework based on the lectures (18 h over 8 weeks)
• Spectroscopy workshop (Contact = 4 x 2 h over 8 weeks, plus self-study time ca. 18 h, plus In-class test assessed workshop 2 h)
• General student independent study.
Indicated Lecture Hours (which may also include seminars, tutorials, workshops and other contact time) are approximate and may include in-class tests where one or more of these are an assessment on the module. In-class tests are scheduled/organised separately to taught content and will be published on to student personal timetables, where they apply to taken modules, as soon as they are finalised by central administration. This will usually be after the initial publication of the teaching timetable for the relevant semester.
Upon accessing the reading list, please search for the module using the module code: CHE3061
Programmes this module appears in
|Chemistry with Forensic Investigation BSc (Hons)||1||Optional||A weighted aggregate mark of 40% is required to pass the module|
|Chemistry BSc (Hons)||1||Compulsory||A weighted aggregate mark of 40% is required to pass the module|
|Medicinal Chemistry BSc (Hons)||1||Compulsory||A weighted aggregate mark of 40% is required to pass the module|
Please note that the information detailed within this record is accurate at the time of publishing and may be subject to change. This record contains information for the most up to date version of the programme / module for the 2021/2 academic year.