Learning Outcomes:
On completion of this module students should have an understanding of:Acidity of Alpha, Beta, Gamma- hydrogens; enolate anion generation, stabilisation; keto/enol tautomerism; halogenation of acetone; alkylation of enolates; regioselctive formation of enolate anions; aldol reactions; claisen reactions; Michael addition chemistry; conjugate addition followed by aldol cyclization; Robinson annelation.Retrosynthetic analysis and how it can be useful in planning synthesis; the application of a range of reactions (nucleophilic substitution, electrophilic aromatic substitution, amide and ester synthesis, addition to carbonyl groups, reactions of nucleophiles with epoxides; reactions of enolates and enols; stereoselective synthesis of alkenes; ring closing and cross metathesis; diels Alder reaction; chemoselectivity and reactions of dianions, reduction of carbonyl compounds; catalytic hydrogenation; oxidation.Laboratory based synthetic organic chemistry with practical and analytical techniques.