About This Course
Course Curriculum
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Introduction00:02:00
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How to read bond-line drawings00:18:00
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How to draw bond-line drawings00:18:00
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Identifying formal charges00:22:00
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Finding lone pairs that are not drawn00:23:00
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What is resonance?00:05:00
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Drawing resonance structures (part 1)00:40:00
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Formal charges in resonance structures00:19:00
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Drawing resonance structures (part 2)00:25:00
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Recognizing patterns00:30:00
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The relative importance of resonance structures00:19:00
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Introduction to acid – base00:03:00
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Charged atoms00:08:00
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Resonance00:11:00
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Induction00:09:00
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Orbitals00:03:00
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Charged atoms – Resonance – Induction – Orbitals00:07:00
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Showing an acid-base mechanism00:14:00
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Acid-Base equilibrium position00:06:00
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Orbitals00:15:00
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Goemetry of orbitals00:15:00
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Impact of resonance on geometry00:01:00
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Introduction to nomenclature00:03:00
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Functional group00:07:00
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Unsaturation00:04:00
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Parent00:09:00
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Substituents00:10:00
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“cis” – “trans” stereoisomerism00:04:00
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“E” – “Z” stereoisomerism00:04:00
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Localizing substituents in parent chain00:12:00
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From structure to name00:20:00
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Introduction to conformations00:02:00
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Newman projection00:10:00
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Relative stability of Newman projections00:08:00
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Drawing chair conformations00:02:00
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Drawing substituents in chair conformations00:12:00
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Ring flipping00:10:00
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Comparing stability of chair conformations00:10:00
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Introduction to configurations00:01:00
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Locating stereocenters00:04:00
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Determining the configuration of a stereocenter00:18:00
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Nomenclature00:12:00
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Enantiomers00:08:00
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Diastereomers00:05:00
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Meso compounds00:04:00
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Fischer projections00:11:00
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Introduction to mechanisms00:02:00
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Nucleophiles and electrophiles00:09:00
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Arrows used for mechanisms00:14:00
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Carbocation00:15:00
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SN1 SN2 mechanisms00:10:00
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Factor #1: the electrophile00:06:00
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Factor #2: the nucleophile00:04:00
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Factor #3: the leaving group00:05:00
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Factor #4: the solvent00:05:00
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Combining all 4 factors00:10:00
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Introduction to elimination reactions00:02:00
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E1 mechanism00:08:00
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E2 mechanism00:20:00
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Introduction to substitution vs elimination00:03:00
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Determining the function of the reagent00:04:00
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Identifying the mechanism(s)00:11:00
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Predicting regiochemical and stereochemical outcomes00:16:00
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Introduction to addition reactions00:01:00
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Regiochemistry00:05:00
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Stereochemistry00:18:00
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Hydrogenation: adding H-H00:07:00
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Hydrohalogenation: adding hydrogen halide, H-X00:09:00
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Hydrobromination : adding H-Br00:09:00
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Hydration: adding H-OH00:12:00
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Adding Br and Br00:05:00
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Halohydrin formation: adding Br and OH00:08:00
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“Anti” dihydroxylation: adding OH and OH00:07:00
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“syn” dihydroxylation : adding OH and OH00:04:00
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Ozonolysis00:03:00
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Reactions summary00:01:00
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One-step synthesis00:03:00
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Combining reactions: changing the position of a leaving group00:03:00
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Combining reactions: changing the position of a double bond00:02:00
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Combining reactions: introducing functionality00:03:00
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Thank you for enrolling and announcing part 200:01:00