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LP-CH2201
LESSON PLAN
LP Rev. No: 00
Date: 25.06.2012
Sub Code & Name : CH2201 – ORGANIC CHEMISTRY
Unit: I
Branch: Chemical Engineering
Page 1 of 6
Semester : III
DOC/LP/01/24.01.09
Objective: To impart the students the knowledge of preparation of various organic compounds,
reaction mechanisms, types and the reagents involved.
Unit syllabus:
Definitions – reagents – mechanism – catalyst – illustration of the following unit
processes: nitration – halogenation - oxidation & reduction – esterification.
Session
No
Time
Topics to be covered
Ref
Teaching
Aids
1
2
3
4
Introduction and concept of IUPAC nomenclature
Common aspects of organic compounds and reactions
Types of reactions – illustration with examples.
Catalyst and its influence on the type of reaction.
50 minutes
50 minutes
50 minutes
50 minutes
T1,R1
T1, R2
T1, R3
R1,R2
BB& C
BB &C
BB&C
BB &C
5
6
7
8
9
Mechanism of nitration in detail with examples.
Mechanism of halogenation in detail with examples.
Mechanisms of redox reactions with examples.
Mechanism of esterification in detail with examples.
Revision and supplementary aspects in Unit I
50 minutes
50 minutes
50 minutes
50 minutes
50 minutes
R2,R3
R1,R3
T1,R1
T1, R2
T1, R3
BB&C
BB &C
BB&C
BB &C
BB&C
LP-CH2201
LESSON PLAN
LP Rev. No: 00
Date: 25.06.2012
Sub Code & Name : CH2201– ORGANIC CHEMISTRY
Unit: II
Branch: Chemical Engineering
Page 2 of 6
Semester : III
DOC/LP/01/24.01.09
Objective: To impart the students the knowledge on the concepts of nucleophile, electrophile,
substitution, condensation and addition reactions.
Unit syllabus: Electrophilic reaction – Friedel craft reaction – Riemer –Tiemenn reaction –
Nucleophilic reactions – aldol condensation – benzoin condensation – Free radical reaction:
Halogenation of alkane – Addition of HBr on alkene in presence of peroxide.
Session
No
Time
Topics to be covered
Ref
Teaching
Aids
50 minutes
T1,R1
BB& C
11
12
13
Concept of nucleophiles and electrophiles; +I and –I
groups – Electrophilic and nucleophilic reactions illustration with examples.
Salient aspects of Friedel craft reactions – examples.
Salient aspects of Riemer-Tiemann reaction- illustration.
Mechanism of aldol condensation reactions – cross aldols.
50 minutes
50 minutes
50 minutes
T1, R2
T1, R3
R1,R2
BB &C
BB&C
BB &C
14
15
16
17
18
Mechanism of benzoin condensation reaction – details.
Mechanism of halogenation of alkanes – details.
Addition of HBr to alkenes - Markovnika rule.
Peroxide effect on HBr addition to alkenes; Revision.
CAT – I
50 minutes
50 minutes
50 minutes
50 minutes
50 minutes
R2,R3
R1,R3
T1,R1
T1, R2
T1, R3
BB&C
BB &C
BB&C
BB &C
BB&C
10
LP-CH2201
LESSON PLAN
LP Rev. No: 00
Date: 25.06.2012
Page 3 of 6
Sub Code & Name : CH2201– ORGANIC CHEMISTRY
Unit: III
Branch: Chemical Engineering
Semester : III
DOC/LP/01/24.01.09
Objective: To impart the students the knowledge of various halogenation, condensation,
polymerization and redox reactions and estimation of important organic compounds.
Unit Syllabus: Allylic halogenation using N.Bromo Succinimide (NBS) – thermal halogenation
of alkene (CH3-CH=CH); condensation and polymerization reactions – oxidation and reduction
reactions – estimation of some organic compounds – phenol – aniline – acetone – glucose.
Session
No
Topics to be covered
Time
19
20
21
22
General aspects of halogenation reactions in detail.
Allylic halogenation using N.Bromo Succinimide (NBS)
Thermal halogenation of alkane / alkene (CH3-CH=CHR)
Condensation and polymerization reactions in detail.
23
24
25
26
27
Oxidation and reduction reactions in detail.
Estimation of phenol – principle and practice.
Estimation of aniline – principle and practice.
Estimation of acetone – principle and practice.
Estimation of glucose – principle and practice.
Ref
Teaching
Aids
50 minutes
50 minutes
50 minutes
50 minutes
T1,R1
T1, R2
T1, R3
R1,R2
BB& C
BB &C
BB&C
BB &C
50 minutes
50 minutes
50 minutes
50 minutes
50 minutes
R2,R3
R1,R3
T1,R1
T1, R2
T1, R3
BB&C
BB &C
BB&C
BB &C
BB&C
LP-CH2201
LESSON PLAN
LP Rev. No: 00
Date: 25.06.2012
Sub Code & Name : CH2201– ORGANIC CHEMISTRY
Unit: IV
Branch: Chemical Engineering
Page 4 of 6
Semester : III
DOC/LP/01/24.01.09
Objective: To impart the students the knowledge of synthesis of important organic compounds.
Unit Syllabus: Synthesis of different types of compounds like alcohol, aldehyde, amine, acids –
dicarboxylic acids – unsaturated acids – synthesis of azodyes – methyl orange and congo dye –
synthesis of triphenyl methane dyes – malachite green – synthesis of alizarin.
Session
No
Time
Topics to be covered
Ref
Teaching
Aids
28
29
30
31
Synthesis of alcohols – detailed approach.
Synthesis of aldehyde – detailed approach.
Synthesis of amine – detailed approach.
Synthesis of acids – dicarboxylic and unsaturated acids.
50 minutes
50 minutes
50 minutes
50 minutes
T1,R1
T1, R2
T1, R3
R1,R2
BB& C
BB &C
BB&C
BB &C
32
33
34
35
36
Synthesis of azodyes – methyl orange – details.
Synthesis of azodyes – congo red – details.
Synthesis of triphenyl methane dyes – malachite green.
Synthesis of alizarin dye and its uses as mordant dyes.
CAT - II
50 minutes
50 minutes
50 minutes
50 minutes
50 minutes
R2,R3
R1,R3
T1,R1
T1, R2
T1, R3
BB&C
BB &C
BB&C
BB &C
BB&C
LP-CH2201
LESSON PLAN
LP Rev. No: 00
Date: 25.06.2012
Sub Code & Name : CH2201– ORGANIC CHEMISTRY
Unit: V
Branch: Chemical Engineering
Page 65 of 6
Semester : III
DOC/LP/01/24.01.09
Objective: To impart the students the knowledge of synthesis and properties of aminoacids and
proteins.
Unit Syllabus: Aminoacids and proteins – classification – synthesis of aminoacids – reactions of
carboxyl and amino group – peptide linkage – end group analysis – colour reaction of proteins –
denaturation.
Session
No
Topics to be covered
Time
37
38
39
40
Aminoacids and proteins – introduction / salient aspects.
Classification of aminoacids and proteins in detail.
Synthetic aspects of aminoacids in detail.
Reactions of aminoacids – those of COOH & NH2 groups
41
42
43
44
45
Reactions of aminoacid –COOH & NH2 groups-combined
Peptide linkage in proteins – detailed discussion.
Colour reactions of proteins – detailed aspects.
Denaturation of proteins – concepts; overall revision.
CAT – III
Ref
Teaching
Aids
50 minutes
50 minutes
50 minutes
50 minutes
T1,R1
T1, R2
T1, R3
R1,R2
BB& C
BB &C
BB&C
BB &C
50 minutes
50 minutes
50 minutes
50 minutes
50 minutes
R2,R3
R1,R3
T1,R1
T1, R2
T1, R3
BB&C
BB &C
BB&C
BB &C
BB&C
Sub Code & Name : CH2201– ORGANIC CHEMISTRY
Semester : III
Branch: Chemical Engineering
DOC/LP/01/24.01.09
Course Delivery Plan:
Week
1
2
3
4
5
6
7
8
9
10
11
12
I II I II I II I II I II I II I II I II I II I II I II
UNIT I
UNIT
Units
II
UNIT III
UNIT
CAT I
I
IV
UNIT V
CAT II
CAT III
Text Book:
1. Tiwari K.S., Vaishnoi N.K. and Marhotra S.N., A Textbook of Organic Chemistry, II edition,
Vikas Publishing House Pvt. Ltd., (1998), New Delhi.
[T1]
References:
1. P.H.Groggins, Unit Processes in Organic Synthesis, III Edition, McGraw-Hill,
New York, 1947.
[R1]
2. Finar I.L. Organic Chemistry – The Fundamental Principles
[R2]
3. Morrison R.T. and Boyd , Organic Chemistry
[R3]
Prepared by
Signature
Name
Designation
Date
Dr. S. Jegannathan & Dr.G.Baskar
Asst. Professors
25.06.2012
Approved by
Staff HOD
Student HOD
Dr. R.Parthiban /
Dr.G.Devasagayam
Prof. & Head
25.06.2012
Dr. R.Parthiban
Prof. & Head
25.06.2012
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