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CHEM-245 Exam 3 Review: Elimination Reactions, NMR & IR Spectroscopy, and Alcohol Reactions
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Alkene Stability
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Heat of Combustion
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Understanding trends of alkene stability.
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Recognizing Different β-Hydrogens
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Identify the number of unique products
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03:19
Identify the number of unique products
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Identify the number of unique products
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E2 Mechanism
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Understanding the properties of E2.
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Drawing the E2 Mechanism.
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Rank reactivity toward E2
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The E1 Mechanism
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03:32
Understanding the properties of E1.
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08:09
Drawing the E1 Mechanism.
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Zaitsev Rule
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Hofmann product
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01:18
Defining Zaitsev’s Rule
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Zaitsev product
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NMR Spectroscopy
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General NMR Features
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1H NMR:Number of Signals
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General Assumption for 1H NMR Signals
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Identifying Proton Signals
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Identifying Proton Signals
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Infrared Spectroscopy
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General Features of IR Spect
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Alcohol Synthesis
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Forming alcohols through SN2 reactions.
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02:02
Forming alcohols through Acid-Catalyzed Hydration.
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Forming alcohols through Hydroboration-Oxidation.
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Leaving Group Conversions - Using HX
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Why do we need to convert Alcohol into a good leaving group?
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Using HX acids via SN2 reaction.
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07:20
Using HX acids via SN1 reaction.
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SN1 Reaction
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Drawing the SN1 Mechanism
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01:13
Why highly substituted leaving groups favor SN1.
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Understanding the properties of SN1.
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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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