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Faculty of Science Handbook, Session 2019/2020

               SIC2015  ELECTROCHEMISTRY                      SIC3002  ORGANIC CHEMISTRY III

               Background of electrochemical cell, type of electrode, liquid   Brief introduction to organic synthesis: disconnections and
               junction  potential,  concentrations  of  electrolyte.  Basic   retrosynthetic analysis;
               electrochemistry on electrode reaction, electrode kinetics,
               Butler-Volmer equation, Tafel anode and cathode equation,   Use of compounds incorporating main group elements (B,
               overpotential, mass transport, diffusion current and Nernst   S, Si, P, mainly; and, Sn, Se, Al) in organic functional group
               diffusion   layer.   Potentiostatic   and   galvanostatic   transformations;
               electrochemical  methods  including  chronoamperometry,   Use of transition metals in C-C bond formation (e.g., Heck,
               coulometry, polarography, cyclic voltammetry and stripping   Suzuki,  Stille,  Negishi,  Sonogashira,  Kumada,  McMurry,
               voltammetry  methods.  Surface  confined  electrochemical   etc.); Alkene metathesis.
               processes and applications in electroanalytical field.
                                                              Stereochemistry:  Introduction  to  asymmetric  synthesis,
               Assessment Methods:                            axial chirality, importance of enantiopure compounds, chiral
               Continuous assessment:    30%                  pool; selected examples of asymmetric synthesis including
               Final examination:      70%                    hydroboration,   hydride   reduction,   hydrogenation,
                                                              epoxidation, dihydroxylation, and aminohydroxylation, use
               Medium of instruction:                         of  chiral  auxiliaries  in  enolate  alkylation,  crossed-aldol
               English                                        additions, and Diels-Alder cycloaddition, etc.

               References:                                    Selected  total  syntheses  of  biologically-active  natural
               1. A. J Bard and L. R. Faulkner, Electrochemical Methods   products  of  contemporary  significance  (e.g.,  taxoids;
                                         nd
                 Fundamental  and  Application,  2   ed.,  John  Wiley  &   macrolides,  e.g.,  epothilones;  Catharanthus  bisindoles;
                 Sons, 2001.                                  prostanoids; steroids; etc.).
               2. D. Pletcher and F. C. Walsh, Industrial Electrochemistry,
                 Blackie Academic and Profesional, 1993.      Physical  organic  concepts  and  methods  in  the
               3. P.  Monk,  Fundamentals  of  Electroanalytical  Chemistry,   determination  of  reaction  mechanisms:  product  studies,
                 John Wiley & Sons, 2001.                     intermediates,  stereochemistry,  energetics  and  kinetics,
                                            nd
               4. J. Wang, Analytical Electrochemistry, 2  ed., John Wiley   isotope  effects  (non-kinetic  and  kinetic),  and,  linear  free
                 & Sons, 2000.                                energy relationships.

                                                              Assessment Methods:
               SIC3001  INORGANIC CHEMISTRY III               Practical:           25%
                                                              Continuous assessment:    15%
               Organometallic Chemistry:                      Final examination:      60%
               Historical  background,  Classification/bonding  types  of
               Organometallics Compounds of Transition Elements, Main   Medium of instruction:
               Group  Organometallics &  Lanthanides,  18-electron  rules,   English
               Ligands   in   Organometallics   (carbonyl,   hydride,
               alkyl/alkene,  carbene,  carbyne,  metallocene  &  fullerene).   References:
               Spectral  (IR,  NMR)  and  x-ray  structural  analysis.   1. Francis  A.  Carey  and  Richard  J.  Sundberg,  Advanced
                                                                                                      th
               Organometallic reactions.                       Organic Chemistry, Part B: Reactions and Synthesis, 4 .
                                                               ed., Plenum Press, New York & London, 2002.
               Reaction  kinetics  and  mechanism  of  transition  metal   2. E. L. Eliel, S. H. Wilen, L. M. Mander, Stereochemistry of
               complexes:                                      Organic Compounds, John Wiley & Sons Canada, Ltd.,
               Introduction to inorganic reaction mechanism. Dissociative,   1994.
               associative and interchange mechanisms. Derivation of the   3. T. H. Lowry, K. S. Richardson, Mechanism and Theory in
                                                                                 rd
               rate  law  based  on  the  above  mechanisms.  Substitution   Organic  Chemistry,  3   ed.,  Benjamin-Cummings
               reactions  of  octahedral,  tetrahedral  and  5-coordinate   Publishing Company, 1987.
               systems. Substitution reactions catalysed by acid and base.    4. J. M. Harris and C. C. Wamser, Fundamentals of Organic
               Inner-sphere and outer-sphere mechanisms.       Reaction Mechanisms, Wiley & Sons, 1976.
                                                                                            nd
                                                              5. N. Isaacs, Physical Organic Chemistry, 2  ed., Prentice
               Assessment Methods:                             Hall, 1996.
               Practical:            25%                      6. S. Warren; P. Wyatt,  Workbook for Organic Synthesis:
               Continuous assessment:    15%                   The Disconnection Approach, 2  ed., John Wiley & Sons,
                                                                                     nd
               Final examination:      60%                     Ltd.: United Kingdom, 2009.

               Medium of instruction:
               English                                        SIC3003  PHYSICAL CHEMISTRY III

               References:                                    Molecular Quantum Mechanics
               1. C.  Elschenbroich  and  A.  Salzer,  Organometallics  A   Approximate  methods:  variational  method  and  time
                                 nd
                 concise Introduction, 2  rev., VCH, 1992.    independent  Perturbation  theory;  Electronic  structure  of
               2. G.  O.  Spessard  and  G.  L.  Miessler,  Organometallic   molecules:  Born-Oppenheimer  approximation,  molecular
                 Chemistry, Prentice Hall, 1997.              orbital  theory,  valence-bond  theory,  Huckel  molecular
               3. Gary L. Miessler & Donald A. Tarr, Inorganis Chemistry.   orbital  theory,  electron  configuration,  Slater  determinant,
                  rd
                 3  ed., Pearson Prentice Hall, 2004          angular  momentum  coupling,  molecular  term  symbols,
               4. F.  A.  Cotton  and  G.  Wilkinson,  Advanced  Inorganic   spin-orbit  and  other  interactions,  molecule  spectra  and
                 Chemistry, John Wiley & Sons, 1972.          selection rules; Hartree-Fock self-consistent-field method,
               5. Journal of Organometallic Chemistry.        other ab initio methods and hybrid systems.
               6. Fred  Basolo  and  Ralph  G  Pearson,  Mechanism  of
                 Inorganic  Reactions.  A  study  of  metal  complexes  in   Molecular Approach to Thermodynamics
                        nd
                 solution, 2  ed., John Wiley & Sons, 1967.   The  fundamentals  of  statistical  mechanics  from  the
               7. R.  A.  Henderson,  The  mechanisms  of  reactions  at   definitions of molecular interactions giving a set of energy
                 transition metal sites, Oxford Science Publications, 1993.   levels  for  N-molecule  systems.  Statistical  treatment  to
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