Organic Chemistry

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About Course

Organic Chemistry (OC) is defined as the branch of chemistry, originally limited to substances found only in living organisms, dealing with the compounds of carbon.

  • What’s with all the hype?

Most science majors would have to undergo an (OC)  module which has been proven to be a very daunting and challenging field to excel in. Students often struggle to even pass the subject. Organic Chemistry can get progressively tough especially when the core foundation is not strong.

  • So why should you take this course?

This isn’t a typical organic chemistry course where I explain to you concepts just for you to memorize. I’ll make you understand the most basic principles and show you how simple questions are when you’ve got your foundation solid. In addition, I’ll drop some tips and tricks for typical questions so that you have it all covered! At the end of the course, you’ll be able to take your exam in absolute confidence and get superb grades!

Who this course is for:

  1. Anyone and everyone who is interested! This is a basic course that covers the underlying principles of organic chemistry for the high-schoolers or even the pre-meds!
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What Will You Learn?

  • Take your exam in absolute confidence and get superb grades!
  • Have a strong foundation in organic chemistry, ready to take more advances courses

Course Content

Organic Chemistry

  • IUPAC Nomenclature of Alkanes: Part 1
    00:00
  • IUPAC Nomenclature of Alkanes: Part 2
    00:00
  • IUPAC Nomenclature of Haloalkanes and Alcohols
    00:00
  • IUPAC Nomenclature of Alkenes and Alkynes
    00:00
  • IUPAC Nomenclature of Cyclic Compounds
    00:00
  • Resonance Structures/Assigning Formal Charge
    00:00
  • Conformational Analysis of Ethane and Butane – Newman Projections
    00:00
  • Cyclohexane Chairs
    00:00
  • Stereochemistry: Enantiomers
    00:00
  • Cahn-Ingold-Prelog Convention (Determining R/S)
    00:00
  • Stereochemistry: Meso Compounds, Diastereomers
    00:00
  • Nucleophiles, Electrophiles, Leaving Groups, and the SN2 Reaction
    00:00
  • SN1 Reaction
    00:00
  • E2 Reaction
    00:00
  • E1 Reaction
    00:00
  • Choosing Between SN1/SN2/E1/E2 Mechanisms
    00:00
  • E2 on Cyclic Systems
    00:00
  • Zaitsev and Hofmann Elimination Products
    00:00
  • E/Z Absolute Configuration of Alkenes
    00:00
  • Carbocation Rearrangement – Hydride and Methanide Shifts
    00:00
  • Addition Reactions
    00:00
  • Hydrohalogenation, Hydration, Dihalogenation
    00:00
  • Addition on Conjugated Polyunsaturated Systems
    00:00
  • Hydrogenation of Alkynes
    00:00
  • Halohydrin Formation
    00:00
  • Oxymercuration-Demercuration
    00:00
  • Hydroboration-Oxidation
    00:00
  • Alkyne Synthesis by Double Dehydrohalogenation
    00:00
  • Williamson Ether Synthesis
    00:00
  • Diels-Alder Cycloaddition
    00:00
  • Ozonolysis
    00:00
  • Oxidation and Reduction
    00:00
  • Aldol Condensation
    00:00
  • Michael Addition
    00:00
  • Robinson Annulation
    00:00
  • Regioselective Enolization and Thermodynamic vs. Kinetic Control
    00:00
  • Claisen Condensation and Dieckmann Condensation
    00:00
  • Reactions of Beta-Dicarbonyl Compounds
    00:00
  • Aromaticity and Huckel’s Rule
    00:00
  • Free Radicals
    00:00
  • Free Radical Halogenation
    00:00
  • Anti-Markovnikov Hydrohalogenation
    00:00
  • Electrophillic Aromatic Substitution
    00:00
  • Friedel-Crafts Alkylation
    00:00
  • Friedel-Crafts Acylation
    00:00
  • Ortho/Meta/Para Directors
    00:00
  • Clemmensen Reduction
    00:00
  • Grignard Reaction
    00:00
  • Wittig Reaction
    00:00
  • IR Spectroscopy
    00:00
  • NMR Spectroscopy
    00:00
  • Homotopic, Enantiotopic, Diastereotopic, and Heterotopic Protons
    00:00
  • Mass Spectrometry
    00:00
  • Reactions of Epoxides
    00:00
  • Hemiacetals, Acetals, and Imines
    00:00
  • Retrosynthetic Analysis
    00:00
  • Leaving Group Derivatives
    00:00
  • Protecting Groups
    00:00
  • Nomenclature of Polycyclic Compounds: Naphthalene, Biphenyl, Anthracene, Spiro, Bicyclo
    00:00
  • More Examples Using the Cahn-Ingold-Prelog Convention
    00:00
  • More Practice With H-NMR Spectra
    00:00
  • Chiral Molecules With No Chiral Centers
    00:00
  • Separating Components of a Mixture by Extraction
    00:00
  • Thin Layer Chromatography (TLC)
    00:00
  • Column Chromatography
    00:00
  • Separating Liquids by Distillation
    00:00
  • Recrystallization
    00:00
  • Nucleophilic Aromatic Substitution
    00:00
  • Carboxylic Acids and Their Derivatives
    00:00
  • Carbonic Acid Derivatives
    00:00
  • Properties of Amides
    00:00
  • Assigning R/S on Fischer Projections
    00:00
  • Fischer Esterification and Saponification
    00:00
  • Organolithium Reagents
    00:00
  • Organocuprates (Gilman Reagents)
    00:00
  • Stereospecificity vs. Stereoselectivity and Regiospecificity vs. Regioselectivity
    00:00
  • Oxidation of Alkenes Using Potassium Permanganate (Hot and Cold Conditions)
    00:00
  • Hofmann Elimination via Exhaustive Methylation of Amines
    00:00
  • Beckmann Rearrangement
    00:00
  • Baeyer-Villiger Oxidation
    00:00

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