Course Curriculum
- 16 sections
- 82 lectures
- 00:00:00 total length
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Introduction
00:02:00
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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
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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
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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
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Orbitals
00:15:00 -
Goemetry of orbitals
00:15:00 -
Impact of resonance on geometry
00:01:00
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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
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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
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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
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Introduction to mechanisms
00:02:00 -
Nucleophiles and electrophiles
00:09:00 -
Arrows used for mechanisms
00:14:00 -
Carbocation
00:15:00
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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
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Introduction to elimination reactions
00:02:00 -
E1 mechanism
00:08:00 -
E2 mechanism
00:20:00
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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
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Introduction to addition reactions
00:01:00 -
Regiochemistry
00:05:00 -
Stereochemistry
00:18:00 -
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 -
“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
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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
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Thank you for enrolling and announcing part 2
00:01:00
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Assignment -Organic Chemistry Demystified
00:00:00