orbitals and mechanism 1 - university of...
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Orbitals and Mechanism 1 Dr Robert Paton [email protected] http://paton.chem.ox.ac.uk
Digital versions of handouts and supplementary material will be made available for download: http://paton.chem.ox.ac.uk/teaching
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Orbitals and Mechanism 1
http://paton.chem.ox.ac.uk 1
Course Outline:
These eight lectures focus on structure, to develop the ability to understand & predict reactivity before the
introduction of new functional group transformations and experimental detail. Overall the lectures will:
introduce curly arrow formalisms for organic reactions; provide an overview that unifies the classical
mechanisms through the primitive steps that are common to each; link this with simple MO concepts and
with stereochemical features of mechanism.
Lecture 1: Acids: equilibrium, pKa, resonance effects. Phenols, C-H bond acidity. Importance of solvent.
Lecture 2: Bases: pKaH, amines, amides, anilines – resonance and inductive effects.
Lecture 3: Basic thermodynamics, reaction diagrams, transition states and intermediates, kinetic vs.
thermodynamic control. Hammond postulate. Reactivity: polarity in molecules, nucleophilicity &
electrophilicity. Electrophiles (El) and nucleophiles (Nu). Relate to FMO interactions/relative energies and
electronegativity, ±I & ±M. Consequences of conjugation; vinylogy.
Lecture 4: Reactions: curly arrow rules illustrated with simple one-step processes. ‘Neutralisation reactions’
and non-charged counterparts. The concept of electron flow. Atoms bearing formal charges do not
necessarily react according to that charge (a-atom activation: eg R2C=OH+, BH4–). Where do the electrons
come from and go? Homing-in on reaction sites: filled and empty orbitals, HOMO & LUMO add a 3D aspect
to mechanism. Relate mechanism with structure as a natural consequence of FMO interactions.
Lecture 5: The importance of the reaction medium. Refer to earlier acid/base discussion. Solvent effects on
neutral and charged species, ability to promote ionisation, counterions. Reactive intermediates: C–, C•, C+.
A unified approach to mechanism. Real examples to illustrate [A+ + B–] (neutralisation) and its exact reverse
(ionisation) leads to SN1. Generalise [A+ + B:] & [A + B–] etc leads to 1,2-addition to C=O and b-elimination
(E1cB, E2). Extension of this leads to SN2. MO discussion as appropriate.
Lecture 6: The case of B: = an alkene. Electrophilic addition with H+ giving a cation leads to discussion of
cation structure, stabilisation & regiochemistry. Hyperconjugation. Exact reverse leads to E1 mechanism. El+
where El bears a lone pair (El = Cl, Br, I) leads to bridged ions and directionality in their opening,
stereospecificity.
Lecture 7: Special case where C=C + El+ is followed by loss of H+ leads to SEAr. Attack by neutral species I
(carbenes, dienes) = pericyclic (should follow naturally from Br2 attack). Attack by neutral species II
(radicals), orientation.
Lecture 8: Review of mechanism types setting the scene for the rest of the course. Redox concepts –
prelude to carbonyl course.
General Texts: Clayden, Greeves, Warren and Wothers, Organic Chemistry, OUP; Keeler and Wothers,
Why Chemical Reactions Happen, OUP
Primers: Hornby and Peach, Foundations of Organic Chemistry OCP #9; Meakins, Functional Groups:
Characteristics and Interconversions, OCP #35; Hornby and Peach, Foundations of Organic Chemistry:
Worked Examples, OCP #87; Robinson, Organic Stereochemistry, OCP #88.
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