Page 167 - Handbook Bachelor Degree of Science Academic Session 20202021
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Faculty of Science Handbook, Session 2019/2020

               Non-spectroscopic techniques:                  rearrangements, and cycloadditions, including tandem and
               Concept of magnetic dipoles and magnetic susceptibility,   cascade processes, in organic synthesis.
               Ideal  paramagnets  (Curie  Law)  and  weakly  interacting
               paramagnets (Curie-Weiss), types of magnetic response,   Assessment Methods:
               experimental  techniques  of  magnetic  susceptibility   Practical:       25%
               measurements in solution and solid state.      Continuous assessment:    15%
               Other  related  methods,  eg.  xray  diffractometry,  PXRD,   Final examination:      60%
               mass spectrometry.
                                                              Medium of instruction:
               Assessment Methods:                            English
               Practical:            25%
               Continuous assessment:    15%                  References:
               Final examination:      60%                    1. F.  A.  Carey  and  R.  J.  Sundberg,  Advanced  Organic
                                                                                                  th
                                                               Chemistry,  Part  B:  Reactions  and  Synthesis,  5 .  Ed.,
               Medium of instruction:                          Plenum Press, New York & London, 2010.
               English                                        2. E.L. Eliel, S.H. Wilen, L.M. Mander, Stereochemistry of
                                                               Organic Compounds, John Wiley & Sons Canada, Ltd.,
               References:                                     1994.
               1. C.  M.  A.  Brett  and  A.  M.  O.  Brett,  Electrochemistry   3. T.H. Lowry, K.S. Richardson, Mechanism and Theory in
                 Principles, Methods and Applications, Oxford Uni. Press   Organic  Chemistry,  3   Ed.,  Benjamin-Cummings
                                                                                 rd
                 Inc., 1993.                                   Publishing Company, 1987.
               2. P.  T.  Kissinger  and  W.  R.  Heinemmen,  Laboratory   4. J.M. Harris and C.C. Wamser, Fundamentals of Organic
                 Techniques  in  Electroanalytical  Chemistry,  Marcel   Reaction Mechanisms, Wiley & Sons, 1976.
                 Dekker Inc., 1984.                           5. Warren, S.; Wyatt, P. Workbook for Organic Synthesis:
               3. D. Pletcher and F.C. Walsh, Industrial Electrochemistry,   The Disconnection Approach, 2nd ed., John Wiley &
                 Blackie Academic and Professional, 1993.      Sons, Ltd.: United Kingdom, 2009.
               4. D. B. Hibbert, Introduction to Electrochemistry, MacMillan   6. R. B. Woodward, R. Hoffmann, The Conservation of
                 Press Ltd., 1993.                             Orbital Symmetry, Academic Press Inc., 2014 (reprint).
               5. K. B. Oldham, J. C. Myland, A. M. Bond, Electrochemical
                 Science   and   Technology:   Fundamentals   and   SID3003  ADVANCED PHYSICAL CHEMISTRY
                 Applications, John Wiley & Sons, Ltd, 2011.
                                                              Molecular Quantum Mechanics
                                                              Approximate  methods:    variational  method  and  time
               SID3002  ADVANCED ORGANIC CHEMISTRY            independent  Perturbation  theory;    Electronic  structure  of
                                                              molecules:  Born-Oppenheimer  approximation,  molecular
               Brief introduction to organic synthesis: disconnections and   orbital  theory,  valence-bond  theory,  Huckel  molecular
               retrosynthetic analysis.                       orbital  theory,  electron  configuration,  Slater  determinant,
                                                              angular  momentum  coupling,  molecule  terms,  spin-orbit
               Use of compounds incorporating main group elements (B,   and  other  interactions,  symmetry,  molecule  spectra  and
               S, Si, P, mainly; and, Sn, Se, Al) in organic functional group   selection rules; Hartree-Fock self-consistent-field method,
               transformations;                               other ab initio methods and hybrid systems.
               Use of transition metals in C-C bond formation (e.g., Heck,
               Suzuki,  Stille,  Negishi,  Sonogashira,  Kumada,  McMurry,   Molecular Approach to Thermodynamics
               etc.); Alkene metathesis.                      The  fundamentals  of  statistical  mechanics  from  the
                                                              definitions of molecular interactions giving a set of energy
               Stereochemistry:  Introduction  to  asymmetric  synthesis,   levels  for  N-molecule  systems.    Statistical  treatment  to
               axial chirality, importance of enantiopure compounds, chiral   obtain  a  distribution  of  the  most  probable  energy
               pool; selected examples of asymmetric synthesis including   configuration or    Boltzmann distribution.  Introduction to
               hydroboration,   hydride   reduction,   hydrogenation,   partition function of molecules containing all the information
               epoxidation, dihydroxylation, and aminohydroxylation, use   on N-molecule systems.  Ensemble concept, incorporated
               of  chiral  auxiliaries  in  enolate  alkylation,  crossed-aldol   partition  function  and  its  relation  to  thermodynamic
               additions, and Diels-Alder cycloaddition, etc.    properties.  Intermolecular  forces  for  various  systems
                                                              including liquid and soft matters. Simple applications of this
               Selected  total  syntheses  of  biologically-active  natural   method in various chemical problems.
               products  of  contemporary  significance  (e.g.,  taxoids;
               macrolides,  e.g.,  epothilones;  Catharanthus  bisindoles;   Application
               prostanoids; steroids; etc.).                    Chemical  Kinetics  and  the  Dynamics  of  Reactions
                                                               Diffusion controlled reactions.  Activated complex theory
               Reactive  intermediates  in  organic  chemistry  including   and  reactions  in solutions.  The  dynamics  of molecular
               carbocations, free radicals, carbenes, nitrenes, and radical-  collisions.   The   kinetics   of   fast   reactions.
               ions. Chemistry of free radicals: reactions and mechanisms   Thermodynamics and kinetics of adsorption.  Structure,
               of   free   radicals   including   abstraction,   addition,   Stability  and  reactivity  in  different  state  of  matter.  The
               rearrangement, cyclization and fragmentation; applications   properties of nonequilibrium.
               of  radical  reactions  in  organic  synthesis;  reactions  of
               carbenes,  carbenoids,  nitrenes,  and  ion-radicals,  and     Photochemistry
               applications  in  synthesis.  Formation,  stability,  and   Kinetics of photophysical and photochemical processes.
               rearrangements  of  carbocations;  tandem  and  cascade   Timescales  of  photophysical  process,  quantum  yield,
               cyclizations.  Mechanistic  details  of  selected  classes  of   mechanism  of  decay  of  excited  states,  quenching.
               organic  reactions  such  as  nucleophilic  substitution,   Applications   of   photochemistry:   photosynthesis,
               hydrolysis,   polar   rearrangements,   electron-transfer   photosynthesis, photobiology and photomedicine.
               reactions,  photochemical  reactions.  Pericyclic  reactions:
               molecular  orbitals;  conservation  of  orbital  symmetry  in   Assessment Methods:
               concerted reactions; theory (frontier orbital method, use of   Practical:       25%
               correlation  diagrams,  aromatic  transition  state  approach)   Continuous assessment:    15%
               and  applications  of  electrocyclic  reactions,  sigmatropic   Final examination:      60%

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