Structure and Reactivity of Organic Compounds II

Module titleStructure and Reactivity of Organic Compounds II
Module codeBIO2085
Academic year2019/0
Credits15
Module staff

Dr Mark Wood (Convenor)

Duration: Term123
Duration: Weeks

11

Number students taking module (anticipated)

75

Description - summary of the module content

Module description

A vital aim of organic chemistry is to be able to synthesise biologically active molecules. With this in mind, you will explore some of the most important organic reactions used in research laboratories. These reactions, along with those introduced in earlier modules, are then studied in the laboratory. Having been introduced to modern spectroscopic methods for determining the structures of organic molecules, these techniques are then used to identify the compounds you have prepared. Aromatic compounds are central to the structure of a vast number of important organic molecules and the chemistry of these species will also be studied.
This module builds on your knowledge of the basic principles of organic (and inorganic and physical) chemistry (including practical) learned in the first year. In particular, it is assumed that you will have a thorough working knowledge of the basic principles of structural representation, mechanism, reactivity, functional group chemistry and stereochemistry.

Module aims - intentions of the module

This module aims to show you how chemists determine and confirm the structures of organic compounds spectroscopically and to describe a number of key, basic reactions, particularly of molecules that contain carbonyl groups and aromatic compounds. Each part of the module is designed to reinforce and build on earlier material, thereby giving you a sound understanding of the fundamentals of modern organic chemistry.

Intended Learning Outcomes (ILOs)

ILO: Module-specific skills

On successfully completing the module you will be able to...

  • 1. Recall the large variety of carbonyl-containing functional groups and understand their basic reactivity
  • 2. Describe (and estimate) the acidity of ?-hydrogen atoms in the common carbonyl group-containing compounds
  • 3. Discuss the formation of enols and enolates from carbonyl compounds
  • 4. Illustrate the basic reactions of enols and enolates, including their use in C-C bond formation
  • 5. Describe in some detail and use basic spectroscopic techniques (ultraviolet, infrared and NMR [1H and 13C] spectroscopies and mass spectrometry)
  • 6. Explain the synthesis and reactivity of benzenoid aromatic compounds (including substituted derivatives)
  • 7. Explain the synthesis and reactivity of 5 and 6-membered ring aromatic heterocyclic compounds
  • 8. Use the basic practical techniques learned in the first year to prepare organic molecules

ILO: Discipline-specific skills

On successfully completing the module you will be able to...

  • 9. Describe and evaluate approaches to our understanding of organic chemistry with reference to primary literature, reviews and research articles
  • 10. Describe in some detail essential facts and theory across a subdiscipline of the chemical and biosciences
  • 11. Identify critical questions from the literature and synthesise research-informed examples from the literature into written work
  • 12. With some guidance, deploy established techniques of analysis, practical investigation and enquiry within the chemical and biosciences

ILO: Personal and key skills

On successfully completing the module you will be able to...

  • 13. Communicate ideas, principles and theories fluently by written means in a manner appropriate to the intended audience
  • 14. Develop, with some guidance, a logical and reasoned argument with valid conclusions
  • 15. Collect and interpret appropriate data, drawing on a range of sources, with limited guidance

Syllabus plan

Syllabus plan

Section 1 – The first part of the module will examine the influence that the carbonyl group has on other positions in a molecule and in particular, the -carbon. The concept of a-hydrogen acidity will be introduced and illustrated using the pKa values of commonly encountered molecules that contain carbonyl groups. An emphasis will be placed on how this acidity is affected by electronic effects. The generation of enols and enolates will be explained and their use in a wide range of reactions will be explained. These reactions will include, a-hydrogen exchange, racemisation, -halogenation and C-C bond formation. The latter category of reaction will include the common acid and base-catalysed condensation reactions.

Section 2 – Concurrently with part 1 (above), this module will cover the principles behind the spectroscopic techniques which are commonly used in the study and determination of the structure of organic molecules, namely ultraviolet, infrared and NMR (1H and 13C) spectroscopy and mass spectrometry.

Section 3 – The structure and reactivity of benzenoid aromatic compounds will be covered after introduction of the general concept of aromaticity. This section of the module will focus mainly on electrophilic substitution but will also examine the special cases of nucleophilic substitition within these systems. Regiochemical issues associated with the use of substituted benzene derivatives will also be explained.

Section 4 – After introducing the key, basic molecules, the synthesis and reactions of 5 and 6-membered ring heterocyclic systems will be compared and contrasted with the benzene derivatives.

Section 5 – The basic practical techniques learned in the first year will be used to synthesise a range of organic molecules. The reactions used will draw on the chemistry covered in sections 1, 3 and 4 (above) and the experiments will use the spectroscopic techniques covered in section 2 for identification of the reaction products.

Where appropriate, all of the sections above will be illustrated with examples of biological relevance.

Learning and teaching

Learning activities and teaching methods (given in hours of study time)

Scheduled Learning and Teaching ActivitiesGuided independent studyPlacement / study abroad
371130

Details of learning activities and teaching methods

CategoryHours of study timeDescription
Scheduled Learning and Teaching22Lectures
Scheduled Learning and Teaching15Laboratory practicals (5 x 3 hours)
Guided Independent Study12Problem-based coursework
Guided Independent Study6Practical write-ups
Guided Independent Study20Guided reading
Guided Independent Study75Independent reading and revision

Assessment

Formative assessment

Form of assessmentSize of the assessment (eg length / duration)ILOs assessedFeedback method
Discussion of problem sheets2 hours1-7, 9-11, 13-15Oral in lectures

Summative assessment (% of credit)

CourseworkWritten examsPractical exams
06040

Details of summative assessment

Form of assessment% of creditSize of the assessment (eg length / duration)ILOs assessedFeedback method
Problem-based examination602 hours1-7, 9-11, 13-15Written via tutor
Problem sheet 1103 hours1-7, 9-11, 13-15Written
Problem sheet 2103 hours1-7, 9-11, 13-15Written
Laboratory report 18800 wordsAllWritten
Laboratory report 2121200 wordsAllWritten

Re-assessment

Details of re-assessment (where required by referral or deferral)

Original form of assessmentForm of re-assessmentILOs re-assessedTimescale for re-assessment
Problem-based examinationProblem-based examination1-7, 9-11, 13-15August Ref/Def
Problem sheet 1Not applicableNot applicableNot applicable
Problem sheet 2Not applicableNot applicableNot applicable
Laboratory report 1Not applicableNot applicableNot applicable
Laboratory report 2Not applicableNot applicableNot applicable

Re-assessment notes

Deferral – if you miss an assessment for certificated reasons judged acceptable by the Mitigation Committee, you will normally be either deferred in the assessment or an extension may be granted. The laboratory/practical assessments are not deferrable because of their practical nature. The mark given for a re-assessment taken as a result of deferral will not be capped and will be treated as it would be if it were your first attempt at the assessment.

Referral – if you have failed the module overall (i.e. a final overall module mark of less than 40%) you will be required to sit a further examination. The mark given for a re-assessment taken as a result of referral will count for 100% of the final mark and will be capped at 40%.

Resources

Indicative learning resources - Basic reading

  • J. Clayden, N. Greeves and S. Warren, Organic Chemistry (Second Edition), Oxford University Press, 2012, ISBN 0-19-927029-5 (essential core text)
  • J. H. Jones, Core Carbonyl Chemistry, (Oxford Chemistry Primer 47), Oxford University Press, 1997, ISBN 0-19-855959-3
  • D. T. Davies, Aromatic Heterocyclic Chemistry, (Oxford Chemistry Primer 2), Oxford University Press, 1992, ISBN 0-19-855660-8

Module has an active ELE page

Indicative learning resources - Other resources

Lecture notes will be made available via ELE after the lectures have been delivered and all lecture handouts, coursework, past examination papers and practical instructions will also be available at the appropriate time. Model answers to coursework problems will also be provided.

Key words search

Synthesis, structures of organic molecules

Credit value15
Module ECTS

7.5

Module pre-requisites

BIO1345 Structure and Reactivity of Organic Compounds I or NSC1003 Foundations in Natural Science

Module co-requisites

None

NQF level (module)

5

Available as distance learning?

No

Origin date

01/11/2011

Last revision date

14/02/2019