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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