Organic Chemistry Demystified

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See the Curriculum Section for materials and enjoy learning with Imperial Academy.

Course Curriculum

Unit 01: About the Course
Introduction 00:02:00
Unit 02: Drawing Organic Molecules
How to read bond-line drawings 00:18:00
How to draw bond-line drawings 00:18:00
Identifying formal charges 00:22:00
Finding lone pairs that are not drawn 00:23:00
Unit 03: Resonance
What is resonance? 00:05:00
Drawing resonance structures (part 1) 00:40:00
Formal charges in resonance structures 00:19:00
Drawing resonance structures (part 2) 00:25:00
Recognizing patterns 00:30:00
The relative importance of resonance structures 00:19:00
Unit 04: Acid-Base Reactions
Introduction to acid – base 00:03:00
Charged atoms 00:08:00
Resonance 00:11:00
Induction 00:09:00
Orbitals 00:03:00
Charged atoms – Resonance – Induction – Orbitals 00:07:00
Showing an acid-base mechanism 00:14:00
Acid-Base equilibrium position 00:06:00
Unit 05: Geometry
Orbitals 00:15:00
Goemetry of orbitals 00:15:00
Impact of resonance on geometry 00:01:00
Unit 06: Nomenclature
Introduction to nomenclature 00:03:00
Functional group 00:07:00
Unsaturation 00:04:00
Parent 00:09:00
Substituents 00:10:00
“cis” – “trans” stereoisomerism 00:04:00
“E” – “Z” stereoisomerism 00:04:00
Localizing substituents in parent chain 00:12:00
From structure to name 00:20:00
Unit 07: Conformations
Introduction to conformations 00:02:00
Newman projection 00:10:00
Relative stability of Newman projections 00:08:00
Drawing chair conformations 00:02:00
Drawing substituents in chair conformations 00:12:00
Ring flipping 00:10:00
Comparing stability of chair conformations 00:10:00
Unit 08: Configurations
Introduction to configurations 00:01:00
Locating stereocenters 00:04:00
Determining the configuration of a stereocenter 00:18:00
Nomenclature 00:12:00
Enantiomers 00:08:00
Diastereomers 00:05:00
Meso compounds 00:04:00
Fischer projections 00:11:00
Unit 09: Mechanisms
Introduction to mechanisms 00:02:00
Nucleophiles and electrophiles 00:09:00
Arrows used for mechanisms 00:14:00
Carbocation 00:15:00
Unit 10: Substitution Reactions
SN1 SN2 mechanisms 00:10:00
Factor #1: the electrophile 00:06:00
Factor #2: the nucleophile 00:04:00
Factor #3: the leaving group 00:05:00
Factor #4: the solvent 00:05:00
Combining all 4 factors 00:10:00
Unit 11: Elimination Reactions
Introduction to elimination reactions 00:02:00
E1 mechanism 00:08:00
E2 mechanism 00:20:00
Unit 12: Substitution vs Elimination
Introduction to substitution vs elimination 00:03:00
Determining the function of the reagent 00:04:00
Identifying the mechanism(s) 00:11:00
Predicting regiochemical and stereochemical outcomes 00:16:00
Unit 13: Addition Reactions
Introduction to addition reactions 00:01:00
Regiochemistry 00:05:00
Stereochemistry 00:18:00
Hydrogenation: adding H-H 00:07:00
Hydrohalogenation: adding hydrogen halide, H-X 00:09:00
Hydrobromination : adding H-Br 00:09:00
Hydration: adding H-OH 00:12:00
Adding Br and Br 00:05:00
Halohydrin formation: adding Br and OH 00:08:00
“Anti” dihydroxylation: adding OH and OH 00:07:00
“syn” dihydroxylation : adding OH and OH 00:04:00
Ozonolysis 00:03:00
Reactions summary 00:01:00
Unit 14: Synthesis Techniques
One-step synthesis 00:03:00
Combining reactions: changing the position of a leaving group 00:03:00
Combining reactions: changing the position of a double bond 00:02:00
Combining reactions: introducing functionality 00:03:00
Unit 15: Wrapping Up and Bonus
Thank you for enrolling and announcing part 2 00:01:00

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Course Info

1 Enrolled
  • Personal Development
  • Teaching & Academics
PRIVATE COURSE
  • PRIVATE
  • 1 year
  • Number of Units81
  • Number of Quizzes0
  • 12 hours, 28 minutes

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