Syllabus: 

Symmetry-adapted orbitals. Mixing rules and buildup approach to molecules and molecular complexes. Energy surface for bond breaking and making. Kinetic vs thermodynamic control, Curtin-Hammett principle, Hammond Postulate Reactive intermediates: Carbocations, carbanions, carbenes, benzyne. Empirical scales for electronic, steric, and solvent effects. Mechanism according to free-energy correlation and correpondence with theory of orbital interaction. Illustrative examples. Linear free energy relationship, Hammett and Taft equations

Text References: 
  1. E. V. Anslyn and D. A. Dougherty, Modern Organic Chemistry, University Science, 2005.
  2. A. Pross, Theory and Physical Principles of Organic Reactivity, John Wiley, 1995.
  3. A. Rauk, Orbital Interaction Theory of Organic Chemistry, John Wiley, 1994.
  4. T. H. Lowry and K. H. Richardson, Mechanisms and Theory in Organic Chemistry, Harper and Row, 1976.

 

Syllabus: 

Symmetry-adapted orbitals. Mixing rules and buildup approach to molecules and molecular complexes. Energy surface for bond breaking and making. Kinetic vs thermodynamic control, Curtin-Hammett principle, Hammond Postulate Reactive intermediates: Carbocations, carbanions, carbenes, benzyne. Empirical scales for electronic, steric, and solvent effects. Mechanism according to free-energy correlation and correpondence with theory of orbital interaction. Illustrative examples. Linear free energy relationship, Hammett and Taft equations

Text References: 

1) E. V. Anslyn and D. A. Dougherty, Modern Organic Chemistry, University
Science, 2005.
2) A. Pross, Theory and Physical Principles of Organic Reactivity, John
Wiley, 1995.
3) A. Rauk, Orbital Interaction Theory of Organic Chemistry, John Wiley, 1994.
4) T. H. Lowry and K. H. Richardson, Mechanisms and Theory in Organic
Chemistry, Harper and Row, 1976.