Module Details

The information contained in this module specification was correct at the time of publication but may be subject to change, either during the session because of unforeseen circumstances, or following review of the module at the end of the session. Queries about the module should be directed to the member of staff with responsibility for the module.
Title Main Group Organic Chemistry
Code CHEM431
Coordinator Dr IA O'Neil
Year CATS Level Semester CATS Value
Session 2022-23 Level 7 FHEQ First Semester 7.5

Pre-requisites before taking this module (or general academic requirements):



The aim of this module is to broaden and extend the knowledge of modern Organic Chemistry so that students will be able to enter directly into a PhD or embark on a career as a specialist chemist.

Learning Outcomes

(LO1) By the end of the module students will have achieved a solid foundation in Organic Chemistry. In particular they will have a clear understanding of Main Group Organic Chemistry and Organopalladium Chemistry and be able to give examples of their use in modern synthetic methodology.

(S1) Students will develop their chemistry-related cognitive abilities and skills, ie abilities and skills relating to intellectual tasks, including problem-solving as required by the Chemistry subject benchmark statement. In particular, at master's level, they will gain the ability to adapt and apply methodology to the solution of unfamiliar problems.

Teaching and Learning Strategies

This module will be delivered by 18 in-person lectures, including revision sessions.
The lecture material is supported by 2 in-person tutorials.

Lectures: 18 hr
Tutorials: 2 hr



Main Group Organic Chemistry
• Chemistry of Lithium: Lithium amide bases, structure and aggregation of organolithiums. Use of sterically hindered bases in controlling enolate formation via kinetic deprotonation. Lithium mediated cyclisation reactions. α-Heteroatom functionalised organolithiums. Transmetallation of organolithiums. Modern application of Grignard reagents.
• Chemistry of Boron: Structure and synthesis of organoboranes. Hydroboration reaction. Reactions of organoboranes. Introduction of heteroatoms via borane intermediates. Use of organoboranes in the synthesis of carbon-carbon bonds. Chemistry of allylboranes.
• Chemistry of Silicon: Comparison of silicon and carbon compounds. Peterson olefination. Chemistry of vinyl, aryl silanes and allylsilanes. Silyl enol ethers, formation and reactions.
• Chemistry of Tin: Synthesis of tin compounds. Transmetallation reactions. Chemistry of vinyl and allyl stannanes. Tin hydr ides and their use in radical mediated reactions.

Organopalladium Chemistry
• Fundamental mechanistic steps: Ligand variation, bonding modes, oxidative addition, reductive elimination, migratory insertion, carbonylation, β-hydride elimination.
• Palladium (II) catalysed C-C formation: Heck simple and tandem processes, isomerisation. Nucleophilic addition to alkenes - Wacker, heterocycle synthesis, catalytic option.
• Palladium (0) catalysed bond formation: C-C Stille and Suzuki couplings with optional carbonylation, Sonogashira alkyne coupling. C-X Formation of amines, sulfides, phosphines etc.
• π-allyl Complexes: Alkylation, mechanism, stereo- and regiochemistry. Carbonates and epoxides - in situ base formation. Intramolecular examples.Trimethylenemethane complexes, [3+2] cycloadditions.

Recommended Texts

Reading lists are managed at Click here to access the reading lists for this module.

Teaching Schedule

  Lectures Seminars Tutorials Lab Practicals Fieldwork Placement Other TOTAL
Study Hours 18


Timetable (if known)              
Private Study 55


EXAM Duration Timing
% of
Penalty for late
No assessment details provided  120    85       
CONTINUOUS Duration Timing
% of
Penalty for late
The coursework consists of one set of assignment problems.    15