ORGANIC STRUCTURE, REACTIVITY AND FUNCTIONAL GROUPS - 2020/1
Module code: CHE1041
In light of the Covid-19 pandemic, and in a departure from previous academic years and previously published information, the University has had to change the delivery (and in some cases the content) of its programmes, together with certain University services and facilities for the academic year 2020/21.
These changes include the implementation of a hybrid teaching approach during 2020/21. Detailed information on all changes is available at: https://www.surrey.ac.uk/coronavirus/course-changes. This webpage sets out information relating to general University changes, and will also direct you to consider additional specific information relating to your chosen programme.
Prior to registering online, you must read this general information and all relevant additional programme specific information. By completing online registration, you acknowledge that you have read such content, and accept all such changes.
Provision of a basic grounding in the canon of organic chemistry, both conceptual and practical.
CUNNINGHAM Ian (Chemistry)
Number of Credits: 15
ECTS Credits: 7.5
Framework: FHEQ Level 4
JACs code: F160
Module cap (Maximum number of students): N/A
Prerequisites / Co-requisites
Indicative content includes:
Structure & bonding
• Bonding in carbon compounds: the C atom, bonds as MOs,
• Energy, electrons and the covalent bond (σ and p bonds)
• Bonding in carbon compounds: hybridisation, sp3, sp2, sp, other atoms, polarization, MOs from ‘filled’ orbitals
• Stereochemistry and conformation
• Reactivity and mechanism: general types, reaction arrows, stabilization of ions and radicals
• Alkenes: structure and reactivity
• Alkenes: additions
• Haloalkanes: nucleophilic substitution and elimination
• The chemistry of alcohols
• Alkanes: free radical halogenation
• The carbonyl group in aldehydes and ketones, nucleophilic addition
• The carbonyl group, α-carbon reactions
• The chemistry of the amines
• The chemistry of the carboxylic acids
• Carboxylic acid derivatives (esters, amides, acid chlorides, acid anhydrides, nitriles)
• The Grignard and related organometallic reactions
Natural product chemistry
• The chemistry of aminoacids
• The chemistry of carbohydrates
• Structure and properties of benzene, introduction to aromaticity, nomenclature of aromatic compounds
• Electrophilic aromatic substitution
• Electrophilic aromatic substitution: directing effects,
• Reactions at the benzylic position
• Aromatic nucleophilic substitution
• Other aromatic systems: naphthalene, heterocyclic aromatic systems, Hückel’s rule
• Multistep reaction examples
• Problem-solving session
Practical organic chemistry (Integrated into the module are basics of organic spectroscopy) comprising a selection of organic experiments such as:
• Hydrolysis of tolunitrile
• Reduction reactions: reduction of 3-nitroacetophenone
• Preparation of cyclohexene by dehydration of cyclohexanol
• Nitration of methylbenzoate
• Preparation of a diazonium salt: Sandmeyer Reaction
|Assessment type||Unit of assessment||Weighting|
|Coursework||Coursework - Laboratory Portfolio||30|
|Examination||Examination (1.5 hours)||70|
Failure in the laboratory component may require reassessment through a defined practical examination.
The assessment strategy is designed to provide students with the opportunity to demonstrate:
• Examination: Application of knowledge to archetypal organic chemistry explanation; and extension of knowledge to a wider range of organic chemistry [LOs 1-3]
• Practicals: Ability carry out basic organic chemistry reactions, and to interpret and analyse them in manner appropriate to the discipline [LOs 1, 2, 4]
Thus, the summative assessment for this module consists of:
• Examination: closed book (70%, 1.5 h)
• Laboratory portfolio: Five stand-alone practicals with 6-7 h in the lab (30%, 35 h plus ca. 10 h write-up
Tutorials: Ability to explain basic principles and to extend these to a wider range of organic chemistry [LOs 1-3].
Formal feedback is provided on tutorial work, optionally on past exam papers and explicitly provided on all aspects of the practical work.
- To provide an introduction to organic chemistry; introducing general concepts of bonding, structure, and reactivity as applied to standard functional groups. In addition it will provide training in, and practice of, basic laboratory procedures.
|001||Recognise basic concepts of structure, bonding and reactivity||K|
|002||Demonstrate an understanding of the concepts by application to specific problems||CK|
|003||Demonstrate an ability to apply concepts to novel situations||C|
|004||Apply basic laboratory techniques to prepare and analyse organic compounds and to report upon it||CKPT|
C - Cognitive/analytical
K - Subject knowledge
T - Transferable skills
P - Professional/Practical skills
Overall student workload
Independent Study Hours: 86
Lecture Hours: 25
Tutorial Hours: 4
Practical/Performance Hours: 35
Methods of Teaching / Learning
The learning and teaching strategy is designed to:
facilitate systematic assimilation of a large volume of information by emphasising atomic/molecular and then mechanistic approaches. This process is designed to allow application to new, but related examples, and is emphasised in the tutorials. The practicals develop skill in basic techniques as well as giving relevance to the lectures.
The learning and teaching methods include:
• Formal lectures (25 hours)
• Practical sessions (35 hours)
• Tutorials (4 hours)
• General self-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.
Reading list for ORGANIC STRUCTURE, REACTIVITY AND FUNCTIONAL GROUPS : http://aspire.surrey.ac.uk/modules/che1041
Programmes this module appears in
|Chemistry BSc (Hons)||2||Compulsory||A weighted aggregate mark of 40% is required to pass the module|
|Chemistry with Forensic Investigation BSc (Hons)||2||Compulsory||A weighted aggregate mark of 40% is required to pass the module|
|Chemistry MChem||2||Compulsory||A weighted aggregate mark of 40% is required to pass the module|
|Chemistry with Forensic Investigation MChem||2||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 2020/1 academic year.