Lesson Structure
Pericyclic Reactions Part 1 (Electrocyclic Reactions)
1.0Â Â Â Â Â Â Â Â Objectives
1.1Â Â Â Â Â Â Â Â Introduction
1.2Â Â Â Â Â Â Â Â Molecular orbital symmetry
1.3Â Â Â Â Â Â Â Â Frontier orbitals of ethylene, 1,3-butadiene, 1,3,5-hexatriene and allyl system.
1.4Â Â Â Â Â Â Â Â Classification of pericyclic reactions.
1.5Â Â Â Â Â Â Â Â Woodward-Hoffmann correlation diagrams
1.5.1Â Â Â Â Correlation diagram Electrocyclic reaction
1.5.2Â Â Â Â Frontier Molecular Orbital (FMO) approach for electrocyclic reactions
1.5.3Â Â Â Â Perturbation Molecular orbital (PMO) approach for electrocyclic reactions(H-M) Huckel-Mobius system
Pericyclic Reactions Part 2 (Cycloadditions and Sigmatropic Reactions)
2.0Â Â Â Â Â Â Â Â Objectives
2.1Â Â Â Â Â Â Â Â Introduction
2.2Â Â Â Â Â Â Â Â Antarafacial and suprafacial additions
2.3        Cycloaddition in 4n π and [4n +2] π system
2.4Â Â Â Â Â Â Â Â 2+2 Cycloaddition Reaction
2.5Â Â Â Â Â Â Â Â cheleotropic reactions
2.5.1Â Â Â Â [2 + 2] Chelotropic cycloaddition
2.6Â Â Â Â Â Â Â Â [1, 3]-dipolar cycloadditions
2.7Â Â Â Â Â Â Â Â Sigmatropic reactions/rearrangement
2.7.1Â Â Â Â Explanation of [1, 3] and [1, 5] sigmatropic shift
2.8Â Â Â Â Â Â Â Â Sigmatropic shifts of alkyl group
2.9Â Â Â Â Â Â Â Â Huckel- Mobius approach in sigmatropic rearrangement
2.10Â Â Â Â Â Â [3,3] sigmatropic rearrangements Cope rearrangements
2.11Â Â Â Â Â Â Claisen rearrangement
2.12Â Â Â Â Â Â [5, 5] rearrangement reactions.
2.13Â Â Â Â Â Â Aza-Cope rearrangements:
2.14Â Â Â Â Â Â Fluxional tautomerism
2.15Â Â Â Â Â Â Ene reaction
CLICK HERE TO DOWNLOAD PDF

Leave A Comment