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Alkenes and Alkynes: Nomenclature, Stability, and Reactions
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Naming Alkenes
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02:04
Name the following alkene
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01:55
How to name alkenes and alkynes
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Cis vs Trans
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Why we need to use the E/Z naming system
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00:50
What does E and Z stand for?
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04:28
How to name different types of double bonds or rings
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E2 Mechanism
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Understanding the properties of E2.
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09:36
Drawing the E2 Mechanism.
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02:03
Rank reactivity toward E2
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Zaitsev Rule
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02:39
Hofmann product
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01:18
Defining Zaitsev’s Rule
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07:01
Zaitsev product
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Dehydrohalogenation
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The dehydrohalogenation mechanism.
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04:35
Dehydrohalogenation mechanism and products
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Dehydration Reaction
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Dehydration of 1° alcohols:The E2 Mechanism
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01:06
An extra note of caution with 1° alcohols.
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06:01
General features of acid-catalyzed dehydration.
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Alkyne Hydration
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Vinyl alcohols yield tautomers.
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03:29
Markovnikov addition of alcohols yields ketones.
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Hydrogenation
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General properties of catalytic hydrogenation.
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Ozonolysis
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06:30
General properties of ozonolysis.
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Preparation of Organometallics
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Ruining Organometallics
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12:21
General Reaction
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Alkynide Synthesis
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03:25
Predict the major product.
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04:17
Provide the reagents needed
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05:09
Predict the major product.
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Nucleophilic Addition
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Nucleophilic Addition
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Reaction Mechanism
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02:39
How to tell if charged molecules will react as nucleophiles or electrophiles.
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01:49
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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