Section 1 : ABOUT THE COURSE
|
|
Lecture 1 | Introduction | 00:01:48 Duration |
Section 2 : DRAWING ORGANIC MOLECULES
|
|
Lecture 1 | How to read bond-line drawings | 00:17:42 Duration |
|
|
Lecture 2 | How to draw bond-line drawings | 00:17:47 Duration |
|
|
Lecture 3 | Identifying formal charges | 00:21:42 Duration |
|
|
Lecture 4 | Finding lone pairs that are not drawn | 00:23:22 Duration |
Section 3 : RESONANCE
|
|
Lecture 1 | What is resonance | 00:04:34 Duration |
|
|
Lecture 2 | Drawing resonance structures (part 1) | 00:39:46 Duration |
|
|
Lecture 3 | Formal charges in resonance structures | 00:19:07 Duration |
|
|
Lecture 4 | Drawing resonance structures (part 2) | 00:24:41 Duration |
|
|
Lecture 5 | Recognizing patterns | 00:29:43 Duration |
|
|
Lecture 6 | The relative importance of resonance structures | 00:19:15 Duration |
Section 4 : ACID-BASE REACTIONS
|
|
Lecture 1 | Introduction to acid-base reactions | 00:02:48 Duration |
|
|
Lecture 2 | Charged atoms | |
|
|
Lecture 3 | Resonance | 00:11:13 Duration |
|
|
Lecture 4 | Induction | 00:08:45 Duration |
|
|
Lecture 5 | Orbitals | 00:02:51 Duration |
|
|
Lecture 6 | Charged atoms - resonance - induction - orbitals | 00:07:10 Duration |
|
|
Lecture 7 | Showing an acid-base mechanism | 00:14:06 Duration |
|
|
Lecture 8 | Acid-base equilibrium position | 00:06:15 Duration |
Section 5 : GEOMETRY
|
|
Lecture 1 | Orbitals | 00:15:12 Duration |
|
|
Lecture 2 | Geometry of orbitals | 00:15:05 Duration |
|
|
Lecture 3 | Impact of resonance on geometry | 00:01:29 Duration |
Section 6 : NOMENCLATURE
|
|
Lecture 1 | Introduction to nomenclature | 00:03:04 Duration |
|
|
Lecture 2 | Functional group | 00:06:30 Duration |
|
|
Lecture 3 | Unsaturation | 00:04:20 Duration |
|
|
Lecture 4 | Parent | 00:08:51 Duration |
|
|
Lecture 5 | Substituents | 00:09:56 Duration |
|
|
Lecture 6 | “cis” - “trans” stereoisomerism | |
|
|
Lecture 7 | “E” - “Z” stereoisomerism | 00:04:03 Duration |
|
|
Lecture 8 | Localizing substituents on parent chain | 00:11:38 Duration |
|
|
Lecture 9 | From structure to name | 00:19:38 Duration |
Section 7 : CONFORMATIONS
|
|
Lecture 1 | Introduction to conformations | 00:01:39 Duration |
|
|
Lecture 2 | Newman projection | 00:10:16 Duration |
|
|
Lecture 3 | Relative stability of Newman projections | 00:07:56 Duration |
|
|
Lecture 4 | Drawing chair conformations | 00:01:54 Duration |
|
|
Lecture 5 | Drawing substituents in chair conformations | 00:11:26 Duration |
|
|
Lecture 6 | Ring flipping | 00:10:17 Duration |
|
|
Lecture 7 | Comparing stability of chair conformations | 00:09:35 Duration |
Section 8 : CONFIGURATIONS
|
|
Lecture 1 | Introduction to configurations | 00:01:23 Duration |
|
|
Lecture 2 | Locating stereocenters | 00:04:21 Duration |
|
|
Lecture 3 | Determining the configuration of a stereocenter | 00:17:45 Duration |
|
|
Lecture 4 | Nomenclature | |
|
|
Lecture 5 | Enantiomers | 00:08:09 Duration |
|
|
Lecture 6 | Diastereomers | |
|
|
Lecture 7 | Meso compounds | 00:03:36 Duration |
|
|
Lecture 8 | Fischer projections | 00:10:33 Duration |
Section 9 : MECHANISMS
|
|
Lecture 1 | Introduction to mechanisms | 00:01:58 Duration |
|
|
Lecture 2 | Nucleophiles and electrophiles | 00:08:35 Duration |
|
|
Lecture 3 | Arrows used for mechanisms | 00:13:37 Duration |
|
|
Lecture 4 | Carbocation | 00:15:11 Duration |
Section 10 : SUBSTITUTION REACTIONS
|
|
Lecture 1 | SN1 SN2 mechanisms | 00:09:35 Duration |
|
|
Lecture 2 | Factor #1 the electrophile | 00:05:56 Duration |
|
|
Lecture 3 | Factor #2 the nucleophile | 00:03:30 Duration |
|
|
Lecture 4 | Factor #3 the leaving group | 00:04:40 Duration |
|
|
Lecture 5 | Factor #4 the solvent | 00:04:50 Duration |
|
|
Lecture 6 | Combining all 4 factors | 00:09:25 Duration |
Section 11 : ELIMINATION REACTIONS
|
|
Lecture 1 | Introduction to elimination reactions | 00:01:46 Duration |
|
|
Lecture 2 | E2 mechanism | 00:20:09 Duration |
|
|
Lecture 3 | E1 mechanism | 00:07:41 Duration |
Section 12 : SUBSTITUTION vs ELIMINATION
|
|
Lecture 1 | Introduction to substitution vs elimination | 00:03:00 Duration |
|
|
Lecture 2 | Determining the function of the reagent | 00:04:11 Duration |
|
|
Lecture 3 | Identifying the mechanism(s) | 00:11:10 Duration |
|
|
Lecture 4 | Predicting regiochemical and stereochemical outcomes | 00:16:18 Duration |
Section 13 : ADDITION REACTIONS
|
|
Lecture 1 | Introduction to addition reactions | 00:01:00 Duration |
|
|
Lecture 2 | Regiochemistry | 00:05:25 Duration |
|
|
Lecture 3 | Stereochemistry | |
|
|
Lecture 4 | Hydrogenation adding H-H | 00:06:38 Duration |
|
|
Lecture 5 | Hydrohalogenation adding hydrogen halide, H-X | 00:09:23 Duration |
|
|
Lecture 6 | Hydrobromination adding H-Br | 00:09:23 Duration |
|
|
Lecture 7 | Hydration adding H-OH | 00:12:10 Duration |
|
|
Lecture 8 | Adding Br and Br | 00:04:43 Duration |
|
|
Lecture 9 | Halohydrin formation adding Br and OH | 00:08:23 Duration |
|
|
Lecture 10 | anti dihydroxylation adding OH and OH | 00:06:46 Duration |
|
|
Lecture 11 | syn dihydroxylation adding OH and OH | 00:03:57 Duration |
|
|
Lecture 12 | Ozonolysis | 00:03:19 Duration |
|
|
Lecture 13 | Reactions summary | 00:01:01 Duration |
Section 14 : SYNTHESIS TECHNIQUES
|
|
Lecture 1 | One-step synthesis | 00:02:35 Duration |
|
|
Lecture 2 | Combining reactions changing the position of a leaving group | 00:02:46 Duration |
|
|
Lecture 3 | Combining reactions changing the position of a double bond | 00:01:56 Duration |
|
|
Lecture 4 | Combining reactions introducing functionality | 00:03:24 Duration |
Section 15 : WRAPPING UP AND BONUS
|
|
Lecture 1 | Thank you for enrolling and announcement for part 2 | 00:00:55 Duration |
