EP106 Organic Chemistry.pdf

Midterm exam will be conducted on week 6 7 week 4 in

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Midterm exam : will be conducted on week 6-7 (week 4 in short semester) of the semester and duration of 1-1.5 hours. Test : will be conducted on week 12-13 (week 6 in short semester) of the semester and duration of 1-1.5 hours. Quizzes : will be conducted at the end of topics and approximately 30 minutes duration.
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Rev December 2016 2 Final Exam component : The Final Exam will consist of 5 compulsory questions. Students must answer all questions within 3 hours. 50% ruling: Applicable Supplementary exam: Applicable (on the final exam only) Mapping of the course to Programme Educational Objectives (PEO) Course Learning Outcomes Programme Objectives PEO 1 PEO 2 PEO 3 CLO 1 CLO 2 CLO 3 CLO 4 Mapping of the course to the Programme Learning Outcomes (PLO) Course Learning Outcomes Programme Learning Outcomes (PLO) 1 2 3 4 5 6 7 8 9 10 11 12 CLO 1 CLO 2 CLO 3 CLO 4 Assessment/CLO Matrix Assessment CLO1 CLO2 CLO3 CLO4 1. Mid-Term exam 2. Test 3. Quiz 4. Final Exam Content outline of the course and the SLT per topic Topic/Content Face to Face Independent Learning TLT L T P O L T P O 1. Aliphatic Hydrocarbons Naming of hydrocarbons (IUPAC method), types of bond, reactivity of bonds, organic derivatives of hydrocarbons. 3.5 - - - 7 - - - 10.5 2. Alkanes and Alkenes : Naming, drawing structures and their properties. .. Hydrogenation, addition of HX (Markovnikov addition), halogenation. hydroboration (anti-Markovnikov addition) 6.5 - - - 13 - - - 19.5 3. Alkynes : Introduction to the alkyne triple bond. Naming, drawing structures and their properties Synthesis and Reactions. Alkylation of acetylide anions (a carbon nucleophile) Addition reactions to alkynes, hydrogenation, halogenation 6.5 - - - 13 - - - 19.5
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Rev December 2016 3 and HX. Hydration of alkynes. 4. Alcohols & Phenols : Naming, drawing structures and their properties Synthesis and reactions; . Acidity (brief review), Synthesis of alcohols. Organometallic reagents, reactivity and basicity. Reaction of carbonyl compounds with Grignard and organolithium reagents.
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  • Spring '10
  • james
  • Benzene, PLO

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