Course Objective(s):
This course will enable the students to -
Course Outcomes (COs):
Course Outcomes |
Teaching Learning Strategies |
Assessment Strategies |
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On completion of this course, the students will be able to-
CO36: discuss the classification, nomenclature, preparation, properties, bonding, structure and applications of simple organometallic compounds and metallic carbonyls. CO37: differentiate between bulk and trace elements, explain the importance of metal ions in biological systems and describe the structure and functions of different metalloenzymes. CO38: describe the structural and chemical properties of five and six membered aromatic heterocycles and active methylene groups CO39: calculate the λmax for different organic compounds using Woodward-Fieser rule. CO40: relate the theoretical knowledge & selection rules of IR to the spectral analysis of simple compounds. |
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Transition Metals: Preparation and important properties of the following compounds-Peroxo compounds of Cr, K2Cr2O7, KMnO4, K4[Fe(CN)6], sodium nitroprusside, [Co(NH3)6]Cl3, Na3[Co(NO2)6].
Organometallic Compounds: Definition, nomenclature and classification of organometallic compounds; Hapticity(η) of organometallic ligands, 18-electron rule. Preparation, properties and structure of alkyls and aryls of Li.
Structure and bonding in metal ethylenic complex–Zeise’s salt (η2) and metal cyclopentadienyl complex- Ferrocene(η5).
Introduction to π acceptor ligands, definition, classification, general methods of preparation, properties, structure and nature of bonding (Synergic effect: VB approach and MO approach) in mononuclear carbonyls.
A brief introduction to bio-inorganic chemistry. Role of metal ions present in biological systems with special reference to Na+, K+ and Mg2+ ions: Na/K pump, role of Mg2+ ions in energy production and chlorophyll (Photosynthesis: PS-I and PS-II), role of Ca2+ in blood clotting, stabilization of protein structures and structural role in bones, Zn (Carboxypeptidase and Carbonic anhydrase- structure and function), metalloporphyrin with special reference to haemoglobin and myoglobin
Nomenclature, aromaticity, synthesis and reactivity of the following compounds with reference to electrophilic and nucleophilic substitution- naphthalene, anthracene, furan pyrrole , thiophene and pyridine.
Introduction, acidity of α- hydrogens, keto-enol tautomerism of ethyl acetoacetate, evidences in favour of keto-enol tautomerism, synthesis of ethylacetoacetate (Claisen condensation) alkylation reaction of ethylacetoacetate and its synthetic uses.
Application of visible, ultraviolet and infrared spectroscopy in organic molecules.
Electromagnetic radiations, electronic transitions, λmax & εmax, chromophore, auxochrome, bathochromic and hypsochromic shifts. Application of electronic spectroscopy and Woodward rules for calculating λmax of conjugated dienes and α,β – unsaturated compounds.
Infrared radiation and types of molecular vibrations, functional group and fingerprint region. IR spectra of alkanes, alkenes and simple alcohols (inter and intramolecular hydrogen bonding), aldehydes, ketones, carboxylic acids and their derivatives (effect of substitution on >C=O stretching absorptions)
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