Page 196 - handbook 20162017
P. 196

Faculty of Science Handbook, Session 2016/2017

               preparation  of  carbonyl,  olefin,  carbene  and  metallocene  epoxidation, dihydroxylation, and aminohydroxylation, use
               complexes; application of organometallics as catalyst.  of  chiral  auxiliaries  in  enolate  alkylation,  crossed-aldol
               Introduction to inorganic reaction mechanism; dissociative,  additions, and Diels-Alder cycloaddition, etc.
               associative  and  interchange  mechanisms;  derivation  of
               rate law; substitution reactions of octahedral, tetrahedral &  Selected  total  syntheses  of  biologically-active  natural
               5-coordinate systems; substitution reactions catalysed by  products  of  contemporary  significance  (e.g.,  taxoids;
               acid   and   base;   inner-sphere   and   outer-sphere  macrolides, e.g.,  epothilones; Catharanthus bisindoles;
               mechanisms                                     prostanoids; steroids; etc.).
               Physical methods in Inorganic Chemistry        Reactive  intermediates  in organic  chemistry  including
               Spectroscopic   techniques:   vibrational,   EPR/ESR,  carbocations,  free  radicals,  carbenes,  nitrenes,  and
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                                   19
               multinuclear NMR (eg. P, F,  119 Sn)           radical-ions.  Chemistry  of  free  radicals:  reactions  and
               Vibrational:  Introduction,  theoretic  background,  selection  mechanisms  of  free  radicals  including  abstraction,
               rules, applications.                           addition,  rearrangement,  cyclization  and  fragmentation;
                                                              applications of  radical  reactions  in  organic  synthesis;
               EPR/ESR:  background,  introduction, electronic  structure  reactions  of  carbenes,  carbenoids,  nitrenes,  and  ion-
               of  atoms  and  open-shell  ions,  spin-orbit  coupling,  g-  radicals, and applications in synthesis. Formation, stability,
               values, Zeeman interaction, hyperfine coupling, hyperfine  and rearrangements of carbocations; tandem and cascade
               anisotropy, applications                       cyclizations.  Mechanistic  details  of  selected  classes  of
               Multinuclear  NMR:  Introduction,  theoretic  background,  organic  reactions  such  as  nucleophilic  substitution,
               applications                                   hydrolysis,   polar   rearrangements,   electron-transfer
                                                              reactions,  photochemical  reactions.  Pericyclic  reactions:
               Non-spectroscopic techniques:                  molecular  orbitals;  conservation  of  orbital  symmetry  in
               Concept of magnetic dipoles and magnetic susceptibility,  concerted reactions; theory (frontier orbital method, use of
               Ideal  paramagnets  (Curie  Law)  and  weakly  interacting  correlation  diagrams,  aromatic  transition  state  approach)
               paramagnets (Curie-Weiss), types of magnetic response,  and  applications  of  electrocyclic  reactions,  sigmatropic
               experimental  techniques  of  magnetic  susceptibility  rearrangements, and cycloadditions, including tandem and
               measurements in solution and solid state.      cascade processes, in organic synthesis.
               Other  related  methods,  eg.  xray  diffractometry,  PXRD,
               mass spectrometry.                             Assessment Methods:
                                                              Continuous assessment:  15%
               Assessment Methods:                            Practical:           25%
               Continuous assessment:  30%                    Final examination:   60%
               Final examination:    70%
                                                              Medium of instruction:
               Medium of instruction:                         English
               English
                                                              Soft skills:
               Soft skills:                                   CT1 – 3
               CT1 – 3
                                                              References:
               References:                                    1. Francis  A.  Carey  and  Richard  J.  Sundberg, Advanced
               1.C.  M.  A.  Brett  and  A.  M.  O.  Brett,  Electrochemistry  Organic  Chemistry,  Part  B:  Reactions  and  Synthesis,
                 Principles, Methods and Applications, Oxford Uni. Press  4 . Ed., Plenum Press, New York & London, 2002.
                                                                th
                 Inc., 1993.                                  2. E.L. Eliel, S.H. Wilen, L.M. Mander, Stereochemistry of
               2.  P.  T.  Kissinger  and  W.  R.  Heinemmen,  Laboratory  Organic Compounds, John Wiley & Sons Canada, Ltd.,
                 Techniques  in  Electroanalytical  Chemistry,  Marcel  1994.
                 Dekker Inc., 1984.                           3. T.H. Lowry, K.S. Richardson, Mechanism and Theory in
               3.  D.   Pletcher   and   F.C.   Walsh,   Industrial  Organic  Chemistry,  3 rd  Ed.,  Benjamin-Cummings
                 Electrochemistry,  Blackie  Academic  and  Professional,  Publishing Company, 1987.
                 1993.                                        4. J.M. Harris and C.C. Wamser, Fundamentals of Organic
               4.  D.  B.  Hibbert,  Introduction  to  Electrochemistry,  Reaction Mechanisms, Wiley & Sons, 1976.
                 MacMillan Press Ltd., 1993.
               5.  K.  B.  Oldham,  J.  C.  Myland,  A.  M.  Bond,
                 Electrochemical   Science   and   Technology:  SID3003 ADVANCED PHYSICAL CHEMISTRY
                 Fundamentals  and  Applications,  John  Wiley  &  Sons,
                 Ltd, 2011.                                   Molecular Quantum Mechanics
                                                              Approximate  methods:    variational  method  and  time
                                                              independent  Perturbation  theory;    Electronic  structure  of
               SID3002 ADVANCED ORGANIC CHEMISTRY             molecules:  Born-Oppenheimer  approximation,  molecular
                                                              orbital  theory,  valence-bond  theory,  Huckel  molecular
               Brief introduction to organic synthesis: disconnections and  orbital  theory,  electron  configuration,  Slater  determinant,
               retrosynthetic analysis.                       angular  momentum  coupling,  molecule  terms,  spin-orbit
                                                              and  other  interactions,  symmetry,  molecule  spectra  and
               Use of compounds incorporating main group elements (B,  selection rules; Hartree-Fock self-consistent-field method,
               S,  Si,  P,  mainly;  and,  Sn,  Se,  Al)  in  organic  functional  other ab initio methods and hybrid systems.
               group transformations;
               Use of transition metals in C-C bond formation (e.g., Heck,  Molecular Approach to Thermodynamics
               Suzuki,  Stille,  Negishi,  Sonogashira,  Kumada,  McMurry,  The  fundamentals  of  statistical  mechanics from  the
               etc.); Alkene metathesis.                      definitions of molecular interactions giving a set of energy
                                                              levels  for  N-molecule  systems.    Statistical  treatment  to
               Stereochemistry:  Introduction  to  asymmetric  synthesis,  obtain  a  distribution  of  the  most  probable  energy
               axial  chirality,  importance  of  enantiopure  compounds,  configuration or    Boltzmann distribution.  Introduction to
               chiral  pool;  selected  examples  of  asymmetric  synthesis  partition  function  of  molecules  containing  all  the
               including hydroboration, hydride reduction, hydrogenation,  information  on  N-molecule  systems.    Ensemble  concept,


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