Section 1 : Organic Chemistry 1 Final Exam Review
Lecture 1 Introduction 1 00:00:51 Duration
Lecture 2 Identifying Functional Groups 00:03:13 Duration
Lecture 3 IUPAC Nomenclature of Alkanes 00:02:27 Duration
Lecture 4 Allylic Carbocation Stability 00:05:22 Duration
Lecture 5 Hybridization Review
Lecture 6 Formal Charge 00:07:02 Duration
Lecture 7 Identifying The Best Lewis Structure 00:04:09 Duration
Lecture 8 Identifying a Pair of Resonance Structures 00:03:02 Duration
Lecture 9 Identifying The Lewis Base 00:05:14 Duration
Lecture 10 Identifying The Strongest Acid 00:12:24 Duration
Lecture 11 EZ IUPAC Nomenclature of Alkenes 00:03:15 Duration
Lecture 12 R & S Configuration 00:07:10 Duration
Lecture 13 Which Reaction Will Yield a Pair of Enantiomers 00:04:14 Duration
Lecture 14 Newman Projections 00:05:23 Duration
Lecture 15 Most Stable Chair Conformation Cis & Trans 00:02:25 Duration
Lecture 16 Which Reaction Will Produce a Racemic Mixture of Products 00:05:59 Duration
Lecture 17 Radical Stability 00:06:15 Duration
Lecture 18 Identifying The Most Acidic Hydrogen 00:01:10 Duration
Lecture 19 Identifying The Most Reactive Substrate In an SN2 Reaction 00:02:55 Duration
Lecture 20 Nucleophilic Substitution Reactions 00:02:40 Duration
Lecture 21 Electrophilic Addition Reactions 00:09:19 Duration
Lecture 22 Hydroboration Oxidation, Regiochemistry and Stereochemistry 00:02:53 Duration
Lecture 23 Bromine In H2O Reaction 00:02:52 Duration
Lecture 24 Initiation, Propagation, and Termination 00:01:37 Duration
Lecture 25 Free Radical Reaction Selectivity of Bromine 00:04:00 Duration
Lecture 26 Free Radical Reactions Using NBS 00:02:10 Duration
Lecture 27 Identifying The Acid With The Lowest pKa 00:01:37 Duration
Lecture 28 Fischer Projections 00:03:39 Duration
Lecture 29 Which Reaction Will Produce a Meso Product 00:05:13 Duration
Lecture 30 Oxidation Reactions 00:01:15 Duration
Lecture 31 Alkyne Reduction Reactions 00:03:09 Duration
Lecture 32 Elimination Reactions 00:11:21 Duration
Lecture 33 E1 Dehydration of Alcohols 00:11:09 Duration
Lecture 34 SN1 Substrate Reactivity 00:01:53 Duration
Lecture 35 Carboxylic Acid Reduction 00:04:02 Duration
Lecture 36 E2 Reaction Stereochemistry 00:03:09 Duration
Lecture 37 E2 Reaction Stereochemistry 2nd Example 00:01:34 Duration
Lecture 38 The Effect of Tripling The Volume on the Rate of a Reaction 00:03:22 Duration
Lecture 39 Electrophilic Addition Reactions Using CH3OH and H+ 00:01:57 Duration
Lecture 40 Electrophilic Addition Reactions Using Br2 and CH3OH 00:02:38 Duration
Lecture 41 Converting an Alkene to a Trans Diol 00:03:46 Duration
Lecture 42 Alkene Reactions With HBr, Br2, NBS, & HBr With Peroxides 00:03:45 Duration
Lecture 43 Oxymercuration Demercuration of Alkynes 00:01:15 Duration
Lecture 44 Dehydration of Alcohols 00:01:11 Duration
Lecture 45 Identifying The Strongest Nucleophile In a Protic Solvent 00:02:36 Duration
Lecture 46 Identifying The Strongest Nucleophile In a Polar Aprotic Solvent 00:01:14 Duration
Lecture 47 Alkyne Synthesis Reactions 00:03:54 Duration
Lecture 48 Carbocation Rearrangements 00:01:37 Duration
Lecture 49 E1 Alcohol Dehydration Reaction Mechanism 00:02:43 Duration
Lecture 50 Polar Protic Solvents vs Polar Aprotic Solvents 00:01:54 Duration
Lecture 51 Leaving Group Trend 00:01:29 Duration
Lecture 52 Hydroboration Oxidation With Deuterium 00:01:25 Duration
Lecture 53 IUPAC Nomenclature of Alcohols 00:01:33 Duration
Lecture 54 Major Resonance Contributor 00:01:17 Duration
Lecture 55 Cis Trans Isomerism 00:03:17 Duration
Lecture 56 Enantiomers, Diastereomers, & Meso Compounds 00:06:02 Duration
Lecture 57 E2 Reaction Problem 00:02:26 Duration
Lecture 58 Alcohol Reactions HBr, PBr3, & TsCl 00:09:24 Duration
Lecture 59 Carbocation Stability & Resonance 00:03:41 Duration
Lecture 60 Carbanion Stability and Resonance 00:02:39 Duration
Lecture 61 Alkyl Chlorides From Alcohols 00:02:16 Duration
Lecture 62 Hydroboration Oxidation and Oxymercuration Demercuration Reaction of Alkynes 00:03:27 Duration
Lecture 63 Alkene + CH3OH Reaction 00:01:20 Duration
Lecture 64 Alkene + CHBr3 KOH With Stereochemistry 00:02:33 Duration
Lecture 65 Alkene + Br2 + H2O Regiochemistry & Stereochemistry
Lecture 66 Enantiomers, Diastereomers, Meso or Identical Molecules 00:00:58 Duration
Lecture 67 Total Number of Stereoisomers Using Chiral Centers 00:02:03 Duration
Lecture 68 Total Number of Stereoisomers Using Alkenes 00:03:18 Duration
Lecture 69 SN2 Reaction of Chair Conformations 00:01:20 Duration
Lecture 70 Identifying All Monochlorinated Products 00:02:44 Duration
Lecture 71 HIO4 Periodic Acid Oxidation 00:01:37 Duration
Lecture 72 HIO4 Reaction Example 00:01:35 Duration
Lecture 73 Ozonolysis of Alkenes 00:01:52 Duration
Lecture 74 KMnO4 Oxidation of Alkenes 00:01:24 Duration
Lecture 75 Ozonolysis of Alkynes 00:01:27 Duration
Lecture 76 Identifying The Alkene Using Reverse Ozonolysis
Lecture 77 Alcohol Oxidation Reactions 00:03:50 Duration
Lecture 78 E2 Reaction of Alkyl Fluorides 00:02:31 Duration
Lecture 79 IUPAC Nomenclature of Bicyclic Compounds 00:03:00 Duration
Lecture 80 Chair, Boat, Twist Boat, and Half Chair Conformation Stability 00:01:05 Duration
Lecture 81 Reduction Reactions 00:03:48 Duration
Lecture 82 Alkyne Synthesis Reactions 00:06:46 Duration
Lecture 83 Reactions of Alcohols Synthesis of Ethers _ Epoxides 00:09:48 Duration
Lecture 84 Formation of Cyclic Ethers From Diols 00:02:10 Duration
Lecture 85 Pinacol Rearrangement 00:02:15 Duration
Lecture 86 Enantiomers, Diastereomers, Meso Compounds Chair Conformation 00:11:13 Duration
Lecture 87 IUPAC Nomenclature of Cycloalkenes 00:01:14 Duration
Lecture 88 Fischer and Newman Projections 00:11:36 Duration
Lecture 89 Which Molecule Has The Highest Boiling Point 00:01:31 Duration
Lecture 90 SN1 Reaction Rate _ Solvent Polarity
Lecture 91 Epoxide Ring Opening Basic Conditions 00:03:21 Duration
Lecture 92 Epoxide Ring Opening Reactions Acidic Conditions 00:04:27 Duration
Lecture 93 Acid Catalyzed Cleavage of Ethers 00:14:03 Duration
Lecture 94 Stereochemistry of E2 Reaction 00:03:42 Duration
Lecture 95 E2 Stereochemistry With Sawhorse Projection 00:03:27 Duration
Lecture 96 E2 Stereochemistry With Chair Conformation
Lecture 97 Which Molecule Has The Highest Dipole Moment 00:04:29 Duration
Lecture 98 Radical Disproportionation Reaction 00:08:04 Duration
Lecture 99 Reduction Reactions 00:08:44 Duration
Lecture 100 Identifying The Most Stable Compound Given The Heat of Combustion 00:02:43 Duration
Lecture 101 Identifying The Unknown Compound 00:04:48 Duration