PT2202 ORGANIC CHEMISTRY AND TECHNOLOGY SYLLABUS | ANNA UNIVERSITY B.TECH. POLYMER TECHNOLOGY 3RD SEMESTER SYLLABUS REGULATION 2008 2011-2012 BELOW IS THE ANNA UNIVERSITY THIRD SEMESTER B.TECH. POLYMER TECHNOLOGY DEPARTMENT SYLLABUS IT IS APPLICABLE FOR ALL STUDENTS ADMITTED IN THE YEAR 2011-2012 (ANNA UNIVERSITY CHENNAI,TRICHY,MADURAI,TIRUNELVELI,COIMBATORE), 2008 REGULATION OF ANNA UNIVERSITY CHENNAI AND STUDENTS ADMITTED IN ANNA UNIVERSITY CHENNAI DURING 2009
PT2202 ORGANIC CHEMISTRY AND TECHNOLOGY L T P C
(Common Polymer & Plastic Technology) 3 1 0 4
AIM
To learn about the various basic organic reactions, their mechanisms, preparation,
properties and uses of monomers.
OBJECTIVES
To get know about the basics of organic chemistry, mechanism of organic
reactions; preparation, properties and uses of majority of the monomers involved
in polymer formation.
UNIT I 12
Structure reactivity and mechanism: Classification and IUPAC Nomenclature of organic
compounds, Functional groups, classification and reactions, Bonding in organic
molecules – Methane, ethylene, acetylene, and butadiene. Polarity of bonds (electron
displacement effect) – Inductive – Electromeric – Conjugative - mesomeric and
Resonance effects. Types of bond breakage- homolysis and heterolysis with examples,
Stereochemistry: General idea of optical and stereoisomerisms, geometrical isomerism.
25
UNIT II 12
Types of reagents- Electrophiles and Nucleophiles, types of reactions – addition
(>C=C<, >C=O) substitution – Electrophilic and Nucleophilic substitution - elimination
and rearrangement reactions – Inter and Intra molecular rearrangement – Hoffman ,
Beckman ,Benzidine rearrangemnts - General conditions and mechanism of each of the
above.
UNIT III 12
Natural gas – Synthesis gas – Petroleum and petroleum products – Coal and coal
products –Cellulose and cellulose products.
Synthesis, properties and uses of Ethylene - Propylene - Butadiene - Vinyl chloride –
Vinylidiene chloride – Vinyl fluoride - Vinylidene fluoride – Vinyl acetate.
UNIT IV 12
Synthesis, properties and uses of – Formaldehyde – Epicholorohydrin - Ethylene oxide -
Propylene oxide – Ethylene glycol, Propylene glycol – Phenol - Bisphenol-A, Phthalic
acid - Adipic acid - Maleic acid - Maleic anhydride - Phthalic anhydride.
UNIT V 12
Synthesis, Properties and uses of Styrene – Hexa Methylene Diamine – Urea – Acrylic
acid - Methacrylic acid - Acrylonitrile - Methyl methacrylate – Tolulenediisocyanate (TDI)-
Hexamethylene di-isocyanate (HMDI)- Diphenyl methane di-isocyanate (MDI).
TOTAL : 60 PERIODS
TEXT BOOKS
1. Morrison & Boyd, “Organic Chemistry”, Prentice Hall. New Delhi, 6th Edition, 1992.
2. B.S.Bahl and Arun Bhal, “Advanced Organic Chemistry”, S. Chand & Co. Ltd., New
Delhi, 15th Edition, 1998
REFERENCES
1. I.L.Finar, “Textbook of Organic Chemistry”, ELBS, 5th edition, 1996.
2. Jerry March, “Advanced Organic Chemistry”, John Wiley & Sons, New York, 1992.
3. A.Brydson, “Plastics materials”, Butterworth - Heinemann – Oxford, 1995.
4. K.J. Saunders, “Organic Polymer Chemistry”, Chapman and Hall Publishers.
PT2202 ORGANIC CHEMISTRY AND TECHNOLOGY L T P C
(Common Polymer & Plastic Technology) 3 1 0 4
AIM
To learn about the various basic organic reactions, their mechanisms, preparation,
properties and uses of monomers.
OBJECTIVES
To get know about the basics of organic chemistry, mechanism of organic
reactions; preparation, properties and uses of majority of the monomers involved
in polymer formation.
UNIT I 12
Structure reactivity and mechanism: Classification and IUPAC Nomenclature of organic
compounds, Functional groups, classification and reactions, Bonding in organic
molecules – Methane, ethylene, acetylene, and butadiene. Polarity of bonds (electron
displacement effect) – Inductive – Electromeric – Conjugative - mesomeric and
Resonance effects. Types of bond breakage- homolysis and heterolysis with examples,
Stereochemistry: General idea of optical and stereoisomerisms, geometrical isomerism.
25
UNIT II 12
Types of reagents- Electrophiles and Nucleophiles, types of reactions – addition
(>C=C<, >C=O) substitution – Electrophilic and Nucleophilic substitution - elimination
and rearrangement reactions – Inter and Intra molecular rearrangement – Hoffman ,
Beckman ,Benzidine rearrangemnts - General conditions and mechanism of each of the
above.
UNIT III 12
Natural gas – Synthesis gas – Petroleum and petroleum products – Coal and coal
products –Cellulose and cellulose products.
Synthesis, properties and uses of Ethylene - Propylene - Butadiene - Vinyl chloride –
Vinylidiene chloride – Vinyl fluoride - Vinylidene fluoride – Vinyl acetate.
UNIT IV 12
Synthesis, properties and uses of – Formaldehyde – Epicholorohydrin - Ethylene oxide -
Propylene oxide – Ethylene glycol, Propylene glycol – Phenol - Bisphenol-A, Phthalic
acid - Adipic acid - Maleic acid - Maleic anhydride - Phthalic anhydride.
UNIT V 12
Synthesis, Properties and uses of Styrene – Hexa Methylene Diamine – Urea – Acrylic
acid - Methacrylic acid - Acrylonitrile - Methyl methacrylate – Tolulenediisocyanate (TDI)-
Hexamethylene di-isocyanate (HMDI)- Diphenyl methane di-isocyanate (MDI).
TOTAL : 60 PERIODS
TEXT BOOKS
1. Morrison & Boyd, “Organic Chemistry”, Prentice Hall. New Delhi, 6th Edition, 1992.
2. B.S.Bahl and Arun Bhal, “Advanced Organic Chemistry”, S. Chand & Co. Ltd., New
Delhi, 15th Edition, 1998
REFERENCES
1. I.L.Finar, “Textbook of Organic Chemistry”, ELBS, 5th edition, 1996.
2. Jerry March, “Advanced Organic Chemistry”, John Wiley & Sons, New York, 1992.
3. A.Brydson, “Plastics materials”, Butterworth - Heinemann – Oxford, 1995.
4. K.J. Saunders, “Organic Polymer Chemistry”, Chapman and Hall Publishers.
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