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UCSI UNIVERSITY 
B.ENG (HONS) IN PETROLEUM ENGINEERING TECHNOLOGY 
COURSE OUTLINE 
Subject name Chemistry for Petroleum Engineering Technology I 
Subject code EG 101 
Status Major 
Credit hour 4 
Semester/Year 2/1 
Pre-requisite None 
Teaching method Lectures & Laboratory 
Assessment Test 1 10% 
Mid Term Examination 20% 
Test 2 10% 
Laboratory 10% 
Final Examination 50% 
The course has four assessment components as described above. 
Test 1: it will be conducted on week 5 of the semester. The test 1 will usually have 4 
questions of approximately 15 minutes duration each. 
Midterm exam: it will be conducted on week 9 of the semester. The midterm exam will have 
4 questions of approximately 20 minutes duration each. 
Test 2: it will be conducted on week 12 of the semester. The test 2 will usually have 4 
questions of approximately 15 minutes duration each. 
Laboratory component: it is compulsory to attend all the lab sessions; failing to do so will 
result in complete failure in the subject. The student will carry out the experiments described 
below and submit a report to the lab tutor. 
Final Exam component: it will consist of 5 questions of 3 hours duration. 
40% ruling: Applicable 
Supplementary exam: Applicable (on the final exam only) 
Lecturer Ms Tan Jully 
Objective This class is a basic introductory to organic chemistry in chemical or petroleum engineering 
study. This unit aims to: 
1. Provide the theory of elements organic chemistry. 
2. Expose to the technique of naming organic compounds according to IUPAC method. 
3. Provide the basic understands physical and chemical properties of the different organic 
compounds which include aliphatic hydrocarbon compounds, aromatic compounds and 
carbonyl compounds. 
4. Provide and expose to the different type of chemical syntheses and reaction mechanisms 
of the aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds. 
5. Explain the importance of carbonyl compounds in industry. 
6. Strengthen their knowledge by performing selected laboratory experiments.. 
7. Pinpoint the basic analytical tools, such as Analytical separation techniques, Gas 
Chromatography, Spectro-photometric principles, HPLC and Atomic absorption. 
Course outcome At the end of the course, students should be able to: 
1. Explain the different type of hybridization. 
2. Explain the different type of compound bonding. 
3. Draw the lewis bonding structure.
4. Naming the organic compounds (aliphatic hydrocarbon compounds, aromatic 
compounds and carbonyl compounds) according to IUPAC methods. 
5. Explain the physical and chemical properties of a specific organic compound 
ranging from aliphatic hydrocarbon compounds, aromatic compounds to carbonyl 
compounds. 
6. Compare difference between organic compounds (aliphatic hydrocarbon 
compound, aromatic compound and carbonyl compounds) based on the physical 
and chemical properties. 
7. Explain the syntheses mechanism of organic compound from a given compound 
(aliphatic hydrocarbon compounds, aromatic compounds and carbonyl 
compounds). 
8. Explain the reaction mechanism of desired product from an compound. (aliphatic 
hydrocarbon compounds, aromatic compounds and carbonyl compounds). 
9. Explain the basic analytical tools such as Analytical separation techniques, Gas 
Chromatography, Spectro-photometric principles, HPLC and Atomic absorption 
and its application. 
Syllabus & 
Contact hour 
1. ALIPHATIC HYDROCARBONS – naming of 
hydrocarbons (IUPAC method), types of bond, 
reactivity of bonds, organic derivatives of 
hydrocarbons. 
2. ALKANES and ALKENES: Recap and Reactions 
The alkene double bond: a focus of reactivity. Polar 
and concerted addition reactions. Hydrogenation, 
addition of HX (Markovnikov addition), halogenation. 
hydroboration (anti-Markovnikov addition) 
3. ALKYNES: Structure and bonding Introduction to the 
alkyne triple bond. 
ALKYNES: Synthesis and Reactions Alkylation of 
acetylide anions (a carbon nucleophile) Addition 
reactions to alkynes, hydrogenation, halogenation and 
HX. Hydration of alkynes. 
4. ALCOHOLS: Structure, synthesis and reactions 
Structure and bonding. Acidity (brief review), 
Synthesis of alcohols. 
Organometallic reagents, reactivity and basicity. 
Reaction of carbonyl compounds with Grignard and 
organolithium reagents .REDOX relationships amongst 
alcohols, aldehydes and ketones and carboxylic acids. 
Alcohols as nucleophiles (formation of alkoxides) and 
electrophiles. Esterification. 
5. AROMATIC COMPOUNDS: Structure and 
Reactions, 2,3 and 4 pi electron systems .Benzene - the 
prototypic aromatic system."aromaticity" Huckel's rule. 
Identifying aromatic systems. Charged and neutral 
species. Polycyclics and heterocyclic. Reaction 
chemistry of aromatic compounds – electrophilic 
Lecture 
3 
6 
3 
6 
8 
Tutorial 
Lab
aromatic substitution: halogenation, nitration, 
sulfonylation and Friedel-Crafts alkylation and 
acylation. Directing effects in electophilic aromatic 
substitution .Nucleophilic aromatic substitution 
.Strategies in the synthesis of multisubstituted benzene 
derivatives. 
6. CARBONYL COMPOUNDS: Summary of various 
types of carbonyl compounds – aldehydes and ketones, 
carboxylic acids and carboxylic acid derivatives (acid 
chlorides, acid anhydrides, esters and amides). 
Synthesis of aldehydes and ketones. Reactions of 
carbonyl compounds with the carbonyl group as an 
electrophile with H, C, N and O nucleophiles. 
8. ANALYTICAL CHEMISTRY: Analytical 
separation techniques, Gas Chromatography, Spectro-photometric 
principles, HPLC and Atomic absorption. 
6 
10 
Total hour 42 28 
Textbook 1. Organic Chemistry (Vol. 1 & II) 6th Edition, by I.L. Finar, Longman Group Ltd. 
London. 
2. Lecture’s Note. 
Reference 1. Organic Chemistry, 9th Edition, T. W. Graham Solomons, University of 
South Florida, Craig B. Fryhle, Pacific Lutheran University. 
2. March’s Advance Organic Chemistry: Reactions, Mechanism and Structure, 
by M.B.Smith and J.March, John Wiley & Sons Inc. 2001. 
Lab session (if 
any) 
1.1 Reaction Stoichiometry 
1.2 Acid Base Titration 
1.3 Crystallization Of A Crude Sample 
1.4 Preparation Of Benzene 
1.5 Simple Distillation For Miscible Mixture 
Matrix CO/PO 
Knowledge & 
Understanding 
Intellectual 
Skills 
Practical Skills 
Transferable 
Skills 
1 2 3 4 5 6 7 1 2 3 4 5 1 2 3 4 5 6 1 2 3 4 
CO/PO A A C B B A C A C B B C A B A 
A: strongly related 
B: Moderately 
C: Slightly

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UCSI University Petroleum Engineering Course Outline for Chemistry 1

  • 1. UCSI UNIVERSITY B.ENG (HONS) IN PETROLEUM ENGINEERING TECHNOLOGY COURSE OUTLINE Subject name Chemistry for Petroleum Engineering Technology I Subject code EG 101 Status Major Credit hour 4 Semester/Year 2/1 Pre-requisite None Teaching method Lectures & Laboratory Assessment Test 1 10% Mid Term Examination 20% Test 2 10% Laboratory 10% Final Examination 50% The course has four assessment components as described above. Test 1: it will be conducted on week 5 of the semester. The test 1 will usually have 4 questions of approximately 15 minutes duration each. Midterm exam: it will be conducted on week 9 of the semester. The midterm exam will have 4 questions of approximately 20 minutes duration each. Test 2: it will be conducted on week 12 of the semester. The test 2 will usually have 4 questions of approximately 15 minutes duration each. Laboratory component: it is compulsory to attend all the lab sessions; failing to do so will result in complete failure in the subject. The student will carry out the experiments described below and submit a report to the lab tutor. Final Exam component: it will consist of 5 questions of 3 hours duration. 40% ruling: Applicable Supplementary exam: Applicable (on the final exam only) Lecturer Ms Tan Jully Objective This class is a basic introductory to organic chemistry in chemical or petroleum engineering study. This unit aims to: 1. Provide the theory of elements organic chemistry. 2. Expose to the technique of naming organic compounds according to IUPAC method. 3. Provide the basic understands physical and chemical properties of the different organic compounds which include aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds. 4. Provide and expose to the different type of chemical syntheses and reaction mechanisms of the aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds. 5. Explain the importance of carbonyl compounds in industry. 6. Strengthen their knowledge by performing selected laboratory experiments.. 7. Pinpoint the basic analytical tools, such as Analytical separation techniques, Gas Chromatography, Spectro-photometric principles, HPLC and Atomic absorption. Course outcome At the end of the course, students should be able to: 1. Explain the different type of hybridization. 2. Explain the different type of compound bonding. 3. Draw the lewis bonding structure.
  • 2. 4. Naming the organic compounds (aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds) according to IUPAC methods. 5. Explain the physical and chemical properties of a specific organic compound ranging from aliphatic hydrocarbon compounds, aromatic compounds to carbonyl compounds. 6. Compare difference between organic compounds (aliphatic hydrocarbon compound, aromatic compound and carbonyl compounds) based on the physical and chemical properties. 7. Explain the syntheses mechanism of organic compound from a given compound (aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds). 8. Explain the reaction mechanism of desired product from an compound. (aliphatic hydrocarbon compounds, aromatic compounds and carbonyl compounds). 9. Explain the basic analytical tools such as Analytical separation techniques, Gas Chromatography, Spectro-photometric principles, HPLC and Atomic absorption and its application. Syllabus & Contact hour 1. ALIPHATIC HYDROCARBONS – naming of hydrocarbons (IUPAC method), types of bond, reactivity of bonds, organic derivatives of hydrocarbons. 2. ALKANES and ALKENES: Recap and Reactions The alkene double bond: a focus of reactivity. Polar and concerted addition reactions. Hydrogenation, addition of HX (Markovnikov addition), halogenation. hydroboration (anti-Markovnikov addition) 3. ALKYNES: Structure and bonding Introduction to the alkyne triple bond. ALKYNES: Synthesis and Reactions Alkylation of acetylide anions (a carbon nucleophile) Addition reactions to alkynes, hydrogenation, halogenation and HX. Hydration of alkynes. 4. ALCOHOLS: Structure, synthesis and reactions Structure and bonding. Acidity (brief review), Synthesis of alcohols. Organometallic reagents, reactivity and basicity. Reaction of carbonyl compounds with Grignard and organolithium reagents .REDOX relationships amongst alcohols, aldehydes and ketones and carboxylic acids. Alcohols as nucleophiles (formation of alkoxides) and electrophiles. Esterification. 5. AROMATIC COMPOUNDS: Structure and Reactions, 2,3 and 4 pi electron systems .Benzene - the prototypic aromatic system."aromaticity" Huckel's rule. Identifying aromatic systems. Charged and neutral species. Polycyclics and heterocyclic. Reaction chemistry of aromatic compounds – electrophilic Lecture 3 6 3 6 8 Tutorial Lab
  • 3. aromatic substitution: halogenation, nitration, sulfonylation and Friedel-Crafts alkylation and acylation. Directing effects in electophilic aromatic substitution .Nucleophilic aromatic substitution .Strategies in the synthesis of multisubstituted benzene derivatives. 6. CARBONYL COMPOUNDS: Summary of various types of carbonyl compounds – aldehydes and ketones, carboxylic acids and carboxylic acid derivatives (acid chlorides, acid anhydrides, esters and amides). Synthesis of aldehydes and ketones. Reactions of carbonyl compounds with the carbonyl group as an electrophile with H, C, N and O nucleophiles. 8. ANALYTICAL CHEMISTRY: Analytical separation techniques, Gas Chromatography, Spectro-photometric principles, HPLC and Atomic absorption. 6 10 Total hour 42 28 Textbook 1. Organic Chemistry (Vol. 1 & II) 6th Edition, by I.L. Finar, Longman Group Ltd. London. 2. Lecture’s Note. Reference 1. Organic Chemistry, 9th Edition, T. W. Graham Solomons, University of South Florida, Craig B. Fryhle, Pacific Lutheran University. 2. March’s Advance Organic Chemistry: Reactions, Mechanism and Structure, by M.B.Smith and J.March, John Wiley & Sons Inc. 2001. Lab session (if any) 1.1 Reaction Stoichiometry 1.2 Acid Base Titration 1.3 Crystallization Of A Crude Sample 1.4 Preparation Of Benzene 1.5 Simple Distillation For Miscible Mixture Matrix CO/PO Knowledge & Understanding Intellectual Skills Practical Skills Transferable Skills 1 2 3 4 5 6 7 1 2 3 4 5 1 2 3 4 5 6 1 2 3 4 CO/PO A A C B B A C A C B B C A B A A: strongly related B: Moderately C: Slightly