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Organic Chemistry Exam Review: Stereochemistry, Reaction Mechanisms, and Molecular Classification
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Meso Compounds
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01:40
Defining meso compounds.
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04:10
The 3 rules of meso compounds.
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03:44
Which of the following molecules are meso?
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Chirality
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03:24
Drawing Mirror Images and Determining Chirality
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05:10
What is chirality?
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03:44
Drawing Mirror Images and Determining Chirality
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Chirality Test 2 - Stereocenters
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Determining Chirality using Stereocenter
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00:36
Determining Chirality using Stereocenter
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02:38
The difference between chiral and trigonal centers.
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Cahn-Ingold-Prelog Nomenclature
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R and S Naming- Step 4
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01:48
Why stereoisomers need their own naming system.
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01:19
Determining Priorities
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Fischer Projection
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Introduction to different projections.
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05:45
How to convert Fischer projections into bondline structures
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03:38
Convert the following Fischer projection into bondline structure.
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Types of Stereoisomers
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Determine total number of stereoisomers
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01:03
How to predict the total number of stereoisomers.
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07:41
Draw stereoisomers and determine relationship
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Reaction Mechanism
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How to tell if charged molecules will react as nucleophiles or electrophiles.
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Nucleophile or Electrophile
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02:48
How to tell if uncharged molecules will react as nucleophiles or electrophiles.
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Introduction to Substitution
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Predict the product
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05:01
Nucleophiles and Electrophiles can react in Bronsted-Lowry Reactions.
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01:47
Nucleophiles and Electrophiles can react in Substitution Reactions.
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The SN2 Mechanism
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Ranking reactivity toward SN2
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08:33
Drawing the SN2 Mechanism
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11:57
Understanding the properties of SN2.
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