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CHM301 Course Information

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0% found this document useful (0 votes)
374 views8 pages

CHM301 Course Information

Must know if you want get A for chm301

Uploaded by

Shahnankacak
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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UNIVERSITI TEKNOLOGI MARA

COURSE INFORMATION

Confidential

Course Code : CHM301

Course Name (English) : ORGANIC CHEMISTRY II APPROVED

Course Name (Malay) : KIMIA ORGANIK II

Course Level : 4 - Diploma

SLT : 120 Hours

Equivalent to 3 Credits

Face to Face: 58 Hours

Non Face to Face: 0 Hours

Student Preparation Time: 62 Hours

Pre-Requisite Courses : No course recommendations

Co-requisite Courses : No co-requisite Courses listed

Equivalent Courses : No equivalent Courses listed

Teaching Period Duration : 17 Weeks

Resource Person : NORDIANA SUHADA BT MOHMAD TAHIRUDDIN

National Education Code : Science, Mathematics and Computing

Delivery Period Duration : 1 Semester

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
Course Learning Outcomes

At the end of the course, students should be able to:

1. Apply the rules in organic chemistry towards nomenclature, structural and chemical reaction of selected organic
compounds. ( C3 )
2. Perform (plan, conduct and analyse) scientific investigation in area of organic chemistry. ( P3 )
3. Outline the reaction mechanisms together with reagents and conditions for the selected chemical reactions. ( C4 )

Course Description

This course is an introductory course on the structure and physical properties of alcohols, carbonyls, carboxylic acids and
derivatives, and amines. This course also includes the nomenclature, preparations, reactions, chemical tests and uses of
the organic compounds.

Syllabus Content

1. Alcohols

1.1 General formula: ROH, ArOH. Nomenclature – common and IUPAC names. Structure: classification of alcohols as
1o, 2o and 3o, functionality of hydroxyl group in the carbon chain e.g. inductive effect of the hydroxyl group.
1.2 Physical properties of alcohols: boiling points and solubility
1.3 Acidity and basicity of alcohols.
1.4 Preparation of alcohols
1.4.1 Grignard synthesis
1.4.2 Hydrolysis of alkyl halides
1.4.3 Industrial and laboratory preparations of ethyl alcohol
1.5 Reactions of alcohols
1.5.1 Formation of alkoxides
1.5.2 Esterification
1.5.3 Dehydration (discuss mechanism)
1.5.4 Halogenation
1.5.5 Oxidation
1.6 Chemical test for 1o, 2o and 3o alcohols

2. Carbonyl Compounds (Aldehydes and Ketones)

2.1 Structure, reactivity and physical properties of carbonyl compounds


2.2 Nucleophilic addition reaction and mechanism
2.3 Nomenclature of aldehydes and ketones
2.4 Preparation of aldehydes
2.4.1 Oxidation of 1o alcohols
2.4.2 Reduction of acid chlorides
2.5 Preparation of ketones
2.5.1 Oxidation of 2o alcohols
2.5.2 Friedal-Crafts acylation
2.6 Reaction of aldehydes and ketones
2.6.1 Oxidation of aldehyde
2.6.2 Reduction to alcohol, Clemensen, Wolff- Kishner
2.6.3 Addition (with HCN, H2O, Grignard Reagent)
2.6.4 Condensation with ammonia derivatives (hydroxylamine, hydrazine phenylhydrazine and
2,4-dinitrophenylhydrazine)
2.6.5 Iodoform reaction
2.7 Chemical test for aldehydes and ketones

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
3. Carboxylic acids

3.1 General formula: RCOOH or ArCOOH


3.2 Nomenclature: IUPAC and trivial names for carboxylic acids
3.3 Physical properties: boiling points and solubility
3.4 Acidity
3.5 Preparation:
3.5.1 Oxidation from alkyl benzenes, alkenes, alcohols and aldehydes
3.5.2 Carboxylation of Grignard reagents
3.5.3 Hydrolysis of nitriles
3.6 Reactions
3.6.1 Salt formation
3.6.2 Reduction
3.6.3 Conversion to acid chlorides
3.6.4 Conversion to esters
3.6.5 Conversion to amides

4. Carboxylic acids derivatives

4.1 General formula: RCO-Z, Nomenclature


4.2 Nucleophilic acyl substitution reactions and mechanism
4.3 Relative reactivity of Nucleophilic acyl substitution reactions

5. Acid chlorides

5.1 General formula: RCOCl


5.2 Nomenclature: IUPAC and trivial name
5.3 Preparation from carboxylic acids
5.4 Reactions
5.4.1 Hydrolysis
5.4.2 Ammonolysis
5.4.3 Alcoholysis
5.4.4 Friedel-Crafts acylation

6. Acid anhydrides

6.1 General formula: (RCO)2O


6.2 Nomenclature
6.3 Preparation from dry salt of carboxylic acid
6.4 Reactions
6.4.1 Hydrolysis
6.4.2 Ammonolysis
6.4.3 Alcoholysis
6.4.4 Friedel-Crafts acylation

7. Esters

7.1 General formula: RCOOR


7.2 Nomenclature: IUPAC and trivial names
7.3 Preparation from:
7.3.1 Carboxylic acids
7.3.2 Acid chlorides
7.4 Reactions
7.4.1 Hydrolysis
7.4.2 Ammonolysis
7.4.3 Grignard reagents
7.4.4 Transesterification

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
8. Amides

8.1 General formula: RCONH2


8.2 Nomenclature
8.3 Preparation from:
8.3.1 Carboxylic acids and ammonium carboxylates
8.3.2 Acid chlorides
8.4 Reactions
8.4.1 Hydrolysis
8.4.2 with nitrous acid
8.4.3 Reduction
8.4.4 Hoffmann degradation
8.4.5 Dehydration
8.5 Chemical tests for carboxylic acids and its derivatives to differentiate amides, acid chlorides, anhydrides and esters

9. Amines

9.1 General formula: RNH2 and ArNH2


9.2 Nomenclature
9.3 Classification of amines: 1o, 2o and 3o
9.4 Preparation
9.4.1 Reduction of nitro compounds
9.4.2 Reduction of halides with ammonia
9.4.3 Reduction of amines
9.4.4 Reduction of nitriles
9.4.5 Hoffmann degradation of amides
9.5 Reactions
9.5.1 Formation of amides
9.5.2 Amine alkylation: Formation of quaternary salts
9.5.3 with nitrous acid
9.5.4 Isocyanides (nitrile compound)
9.5.5 Benzenediazonium salts
9.5.5.1 Preparation of benzenediazonium chloride
9.5.5.2 Reaction of benzenediazonium chloride

Teaching Methodologies

Collaborative Learning
Lab Work
Lectures
Tutorial

Proposed % Marks Approved by KPP

Question Difficulty Levels Range

C1 - C2 10 - 40

C3 - C4 10 - 60

Assessment

Continuous 60.00%
Assessment: Assignment - 20% out of 20 on Week 5. Passing Mark(s): 10
Assignment - Written assignment (2)
CLO: 1

Practical - 15% out of 15 on Week 2. Passing Mark(s): 7


Written report (3) Experiment 1: Reaction of alcohols and phenols, Experiment 2: Reaction of
aldehyde and ketone, Experiment 5: Synthesis of isopentyl acetate (banana oil)
CLO: 2

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
CLO: 2

Practical - 15% out of 15 on Week 2. Passing Mark(s): 7


Direct Observation (Skills)
CLO: 2

Test - 5% out of 5 on Week 6. Passing Mark(s): 3


Test - Written test
CLO: 1

Test - 5% out of 5 on Week 13. Passing Mark(s): 3


Test - Written test
CLO: 3

Final Assessment: 40.00%


Final Examination - 40% out of 60 on End of Semester. Passing Mark(s): 30
Final examination cover all chapters in this subjects
CLO: 1 , 3
Duration : 120 minutes

Transferable Skills

Ability to apply knowledge of science, knowledge of practical skills and solve problem with thinking and scientific skills.

Special Regulation

This Module has no special regulation

Reassessment Requirement

This Module has no Reassessment Requirement

Reassessment Description

This Module has no Reassessment Description

Recommended Text

References

1. Solomon T.W.G., Fryhle C.B. and Synder S.A.,, Organic Chemistry, 12, n/a, 2016, ISBN: 978119233640
2. McMurry J.E., Organic Chemistry, 6, Brooks/Cole, 2016, ISBN: 978130508048
3. Brown W.H., Iverson B.L., Anslyn E. and Foote C.,, Organic Chemistry, 7, Brooks/Cole, 2014, ISBN: 978-113395284
4. Smith J.,, Organic Chemistry, 5, McGraw Hill, 2016, ISBN: 978-00780215
5. Pavia D.L., Lampman G.M., Kriz G.S. and Engel R.G.,, A Small Scale Approach to Organic Laboratory Technique, 4,
Brooks/Cole, 2016, ISBN: 978130525392

Other References

This module does not have other references

Course Extra Information

This Module has no extra information

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
UNIVERSITY TEKNOLOGI MARA

COURSE LEARNING OUTCOMES - MOE LEARNING OUTCOMES - SOFT SKILLS LEARNING OUTCOMES RELATIONSHIP MATRIX

COURSE CODE CHM301 FACULTY / ACADEMY FACULTY OF APPLIED SCIENCES

COURSE NAME (IN ENGLISH) ORGANIC CHEMISTRY II CREDIT UNIT 3

COURSE NAME (IN MALAY) KIMIA ORGANIK II Resource Person NORDIANA SUHADA BT MOHMAD TAHIRUDDIN

  Achievement of MOHE Learning Outcomes Achievement of Soft Skills Learning Outcomes

Course Learning Outcomes (CLO) LO1 LO2 LO3 LO4 LO5 LO6 LO7 LO8 LO9 SS1 SS2 SS3 SS4 SS5 SS6 SS7

Apply the rules in organic


chemistry towards nomenclature,
CLO1 structural and chemical reaction /
of selected organic compounds.
( C3 )

Perform (plan, conduct and


CLO2 analyse) scientific investigation in /
area of organic chemistry.
( P3 )

Outline the reaction mechanisms


together with reagents and
CLO3 conditions for the selected / /
chemical reactions.
( C4 )

Ministry of Education Learning Outcomes Soft Skills Learning Outcomes

i. Knowledge i. Critical Thinking and Problem-solving Skills


ii. Practical Skills ii. Communication Skills
iii. Thinking and Scientific Skills iii. Team Skills
iv. Communication Skills iv. Ethics & Moral Professionalism
v. Social skills, Teamwork and Responsibilities v. Life-long Learning & Information Management
vi. Values, Ethics, Moral and Professionalism vi. Entrepreneurial Skills
vii. Information Management and Life Long Learning vii. Leadership Skills
viii. Management and Entrepreneurship
ix. Leadership Skills

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
UNIVERSITY TEKNOLOGI MARA

COURSE LEARNING OUTCOMES - TAXONOMY LEVELS

COURSE CODE CHM301 FACULTY / ACADEMY FACULTY OF APPLIED SCIENCES

COURSE NAME (IN ENGLISH) ORGANIC CHEMISTRY II CREDIT UNIT 3

COURSE NAME (IN MALAY) KIMIA ORGANIK II Resource Person NORDIANA SUHADA BT MOHMAD TAHIRUDDIN

COGNITIVE PSYCHOMOTOR AFFECTIVE


COURSE OUTCOMES
C1 C2 C3 C4 C5 C6 P1 P2 P3 P4 P5 P6 P7 A1 A2 A3 A4 A5

Apply the rules in organic chemistry


towards nomenclature, structural and
1 chemical reaction of selected organic /
compounds.
( C3 )

Perform (plan, conduct and analyse)


2 scientific investigation in area of organic /
chemistry.
( P3 )

Outline the reaction mechanisms together


3 with reagents and conditions for the /
selected chemical reactions.
( C4 )

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020
UNIVERSITY TEKNOLOGI MARA

COURSE OUTCOMES

COURSE CODE CHM301 FACULTY / ACADEMY FACULTY OF APPLIED SCIENCES

COURSE NAME (IN ENGLISH) ORGANIC CHEMISTRY II CREDIT UNIT 3

COURSE NAME (IN MALAY) KIMIA ORGANIK II Resource Person NORDIANA SUHADA BT MOHMAD TAHIRUDDIN

ACHIEVEMENT OF MOE LEARNING OUTCOMES


COURSE LEARNING OUTCOMES TEACHING METHODOLOGY ASSESSMENT
LO1 LO2 LO3 LO4 LO5 LO6 LO7 LO8 LO9

Apply the rules in organic chemistry towards Lecture Test


1 nomenclature, structural and chemical / Laboratory Assignment
reaction of selected organic compounds. Tutorial Final Examination

Perform (plan, conduct and analyse) scientific Lecture Practical


2 investigation in area of organic chemistry. / Laboratory Practical
Tutorial

Outline the reaction mechanisms together with Lecture Test


3 reagents and conditions for the selected / Laboratory Final Examination
chemical reactions. Tutorial

Faculty Name : FACULTY OF APPLIED SCIENCES Start Year : 2018


© Copyright Universiti Teknologi MARA Review Year : 2020

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