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The [course_title] aims to equip you with the necessary knowledge and experimental skills in organic chemistry required for planning, understanding and conducting organic reactions and separation in addition to structure elucidations of organic compounds. The course will generate deeper knowledge and experimental skill in organic chemistry. So don’t be late to get this course to build your skills and advance your career.


This course does not involve any written exams. Students need to answer 5 assignment questions to complete the course, the answers will be in the form of written work in pdf or word. Students can write the answers in their own time. Each answer needs to be 200 words (1 Page). Once the answers are submitted, the tutor will check and assess the work.


Edukite courses are free to study. To successfully complete a course you must submit all the assignment of the course as part of the assessment. Upon successful completion of a course, you can choose to make your achievement formal by obtaining your Certificate at a cost of £49.

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Course Credit: Yale University

Course Curriculum

Module: 01
1. Mechanism: How Energies and Kinetic Order Influence Reaction Rates 00:49:00
2. Peculiar Rate Laws, Bond Dissociation Energies, and Relative Reactivities 00:48:00
3. Rate and Selectivity in Radical-Chain Reactions 00:46:00
4. Electronegativity, Bond Strength, Electrostatics, and Non-Bonded Interactions 00:50:00
5. Solvation, H-Bonding, and Ionophores 00:47:00
Module: 02
6. Brønsted Acidity and the Generality of Nucleophilic Substitution 00:47:00
7. Nucleophilic Substitution Tools – Stereochemistry, Rate Law, Substrate, Nucleophile 00:52:00
8. Solvent, Leaving Group, Bridgehead Substitution, and Pentavalent Carbon 00:48:00
9. Pentavalent Carbon ? E2, SN1, E1 00:48:00
10. Cation Intermediates. Alkenes: Formation, Addition, and Stability 00:51:00
Module: 03
11. Carbocations and the Mechanism of Electrophilic Addition to Alkenes and Alkynes 00:52:00
12. Nucleophilic Participation During Electrophilic Addition to Alkenes 00:49:00
13. Addition to Form Three-Membered Rings: Carbenoids and Epoxidation 00:51:00
14. Epoxide Opening, Dipolar Cycloaddition, and Ozonolysis 00:50:00
15. Metals and Catalysis in Alkene Oxidation, Hydrogenation, Metathesis, and Polymerization 00:51:00
Module: 04
16. Isoprenoids, Rubber, and Tuning Polymer Properties 00:46:00
17. Alkynes. Conjugation in Allylic Intermediates and Dienes 00:50:00
18. Linear and Cyclic Conjugation Theory. 4n+2 Aromaticity 00:48:00
19. Aromatic Transition States: Cycloaddition and Electrocyclic Reactions 00:49:00
20. Electronic and Vibrational Spectroscopy 00:50:00
Module: 05
21. Functional Groups and Fingerprints in IR Spectroscopy. Precession of Magnetic Nuclei 00:52:00
22. Medical MRI and Chemical NMR 00:49:00
23. Diamagnetic Anisotropy and Spin-Spin Splitting 00:48:00
24. Higher-Order Effects, Dynamics, and the NMR Time Scale 00:48:00
25. C-13 and 2D NMR. Electrophilic Aromatic Substitution 00:50:00
Module: 06
26. Aromatic Substitution in Synthesis: Friedel-Crafts and Moses Gomberg 00:51:00
27. Triphenylmethyl and an Introduction to Carbonyl Chemistry 00:46:00
28. Mechanism and Equilibrium of Carbonyl Reactions 00:49:00
29. Imines and Enamines. Oxidation and Reduction 00:50:00
30. Oxidation States and Mechanisms 00:47:00
Module: 07
31. Periodate Cleavage, Retrosynthesis, and Green Chemistry 00:46:00
32. Measuring Bond Energies: Guest Lecture by Prof. G. Barney Ellison 00:48:00
33. Green Chemistry. Acids and Acid Derivatives 00:49:00
34. Acids and Acid Derivatives 00:50:00
35. Acyl Insertions and [gr]α-Reactivity 00:49:00
Module: 08
36. [gr]α-Reactivity and Condensation Reactions 00:53:00
37. Proving the Configuration of Glucose and Synthesizing Two Unnatural Products 00:55:00
38. Review: Synthesis of Cortisone 00:52:00
Submit Your Assignment 00:00:00
Certification 00:00:00

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