SYNTHETIC STRATEGIES IN ORGANIC CHEMISTRY

Paper Code: 
CHY 144 B
Credits: 
4
Contact Hours: 
60.00
Max. Marks: 
100.00
12.00
Unit I: 
Principles of Green Chemistry I

History, need and goal,  green chemistry and sustainability and background of green chemistry.
Twelve basic principles of green chemistry with their explanation and examples and special emphasis on the following- designing a green synthesis using these principles, prevention of waste/ byproducts, atom economy- maximum incorporation of the materials used in the process into the final products, calculation of atom economy of the rearrangement, addition, substitution and elimination reactions.
Prevention/ minimization of hazardous/ toxic products reducing toxicity.
Risk = (Function) hazard x exposure, waste or pollution prevention hierarchy.

 

12.00
Unit II: 
Principles of Green Chemistry II

Green solvents- supercritical fluids, water as a solvent for organic reactions, ionic liquids, fluorous biphasic solvent, PEG, solventless processes, immobilized solvents and how to compare greenness of solvents.
Energy requirements for reactions- alternative sources of energy.
Microwave assisted reactions in water- Hofmann elimination, hydrolysis (of benzyl chloride)
Ultrasound assisted reactions- esterification, saponification, substitution reactions, Alkylations,   oxidation, reduction, coupling reaction, Cannizzaro reaction, Strecker synthesis, Reformatsky reaction.
Selection of starting materials, avoidance of unnecessary derivatization, careful use of blocking/protecting groups.
Use of catalytic reagents in preference to stoichiometric reagents, catalysis and green chemistry, comparison of heterogeneous and homogeneous catalysis, bio catalysis, asymmetric catalysis and photocatalysis.

 

12.00
Unit III: 
Organocatalysts

Definition, generic modes, classification.
Covalent organocatalysis - secondary amines via enamine, imine, imim ion, amidines, guanidines , Lewis base catalysis, nitrogen heterocyclic carbenes (NHC), synthesis, structure, catalysis-homo-and cross-benzoin condensation, Stetter reaction, hydrosilylation of styrenes, transesterification.
Noncovalent organocatalysis- hydrogen bonding catalysis, thiourea based catalysts, Diols- TADDOL.
Phosphorus containing organocatalysts- triphenylphosphine, Binol-derived phosphoric acids, cyclic diphosphazanes, phosphonates.

 

12.00
Unit IV: 
Introduction to Nanomaterials

Emergence of nanotechnology, types of nanomaterials, zero dimensional, one dimensional, two dimensional and three dimensional nanomaterials, composite materials.
Fabrication methods- bottom up and top down approach, solution phase and vapor phase synthesis
Physical methods- physical vapour deposition (evaporation, sputtering and plasma processing methods), chemical vapour deposition, epitaxial growth method, ball miling, lithography.
Chemical methods- sol-gel process, reduction method, self-assembly method, coprecipitation, microemulsion, solvothermal, microwave synthesis, evaporation, template synthesis, sonochemical synthesis, radiation assisted synthesis, chemical etching.
Biological methods- synthesis using microorganism, biological templates, plants and plant            extracts.

 

12.00
Unit V: 
Properties, Characterization and Applications of Nanomaterials

Properties of nanomaterials, surface energy.

Stabilization of nanomaterials- Electrostatic and steric stabilization of nanoparticles, quantum confinement effect, nanocatalyst.
Carbon nanomaterials- fullerenes, graphenes, nanotubes.
Characterization of nanomaterials: Principle, Instrumentation and applications of Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), Atomic Force Microscopy (AFM), Scanning Tunneling Microscopy, X-Ray powder diffraction in the characterization of nanomaterials.

Applications and social impact- Fuel cell, hydrogen production and storage, batteries, capacitors, photoelectrochemical splitting of water, gas sensors, defense, nanomedicines.

References: 
  1. Introduction to Nanotechnology; First Edition; R. Singh and S. M. Gupta; Oxford University Press, 2016.
  2. An Introduction to Nanomaterials and Nanoscience; A. K. Das, M. Das; CBS Publishers and Distributors Private Limited, 2014.
  3. Organic Chemistry, Second edition; J. Clayden, N. Greeves, S. Warren; Oxford University Press, United Kingdom, 2012.
  4. Advanced Organic Chemistry: Reactions, Mechanisms and Structure, Seventh Edition; J. March; John Wiley and Sons Asia Private Limited, New Delhi, 2015.
  5. Green Chemistry: Introductory Text, Third Edition; M. Lancaster; Royal Society of Chemistry (London), 2016.
  1. Advanced Organic Chemistry Part A & B, Fifth Edition; F. A. Carey and R. J. Sundberg; Springer, US, 2007.
  2. Mechanism and Theory in Organic Chemistry; Third Edition; T.H. Lowry; Addison– Wesley Publishing Company, 1999.
  3. Modern Methods of Organic Synthesis; Fourth Edition; W. Carruthers; Cambridge Univ. Press, UK, 2005.
  4. Principles of Asymmetric Synthesis; Second Edition; R. Gawley and J. Aube; New York: Pergamon Press, 2012

 

Academic Year: