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Hückel, AJM
[edit]Understanding Structure and Reactivity, Part 2
- The course looks at carbon 2p orbitals and the π bonds they can form, especially in conjugated systems such as polyenes
- Secular equations — see Quantum Concepts lectures by FRM's predecessor Professor Balint-Kurti: GGBK lecture 6
- Hückel method
- Pericyclic reactions: ChemTube3D - Jmol animations of pericyclic reactions
- Woodward–Hoffmann rules: a set of rules for predicting the stereochemistry of pericyclic reactions based on orbital symmetry
- Cycloadditions
- Electrocyclic reactions
Typical molecules studied in the course
[edit]- ethylene, C2H4
- 1,3-butadiene, C4H6
- benzene, C6H6
- cyclopropenyl radical, [C3H3]•
- cyclopentadienyl anion, [C5H5]−
- trimethylenemethane,
- this is a non-Kekulé molecule that came up in the 2009 exam
- it's a diradical with a triplet ground state, but can 'rearrange' to methylenecyclopropane via an excited singlet state
- cyclopropenyl cation, [C3H3]+
- cyclobutadiene, C4H4