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Alcohols: Reduction, Oxidation, Grignard Reactions, and Protecting Groups
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Reactions of Organometallics
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13:40
Reactions of Organometallics
Johnny Betancourt
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Leaving Group Conversions - Using HX
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02:03
Why do we need to convert Alcohol into a good leaving group?
Johnny Betancourt
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02:16
Using HX acids via SN2 reaction.
Johnny Betancourt
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30
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18
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07:20
Using HX acids via SN1 reaction.
Johnny Betancourt
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Leaving Group Conversions - SOCl2 and PBr3
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06:01
Predict the mechanism of PBr3, and draw the final product.
Johnny Betancourt
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07:18
Learning the mechanism of SOCl2.
Johnny Betancourt
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Acid-Catalyzed Dehydration
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05:20
Dehydration of 1° alcohols:The E2 Mechanism
Johnny Betancourt
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01:06
An extra note of caution with 1° alcohols.
Johnny Betancourt
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7
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06:01
General features of acid-catalyzed dehydration.
Johnny Betancourt
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Dehydration with Phosphoryl Chloride
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Mechanism of Dehydration with POCl3
Johnny Betancourt
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01:23
General Reaction of Dehydration with POCl3
Johnny Betancourt
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Intro to Redox
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Distinguishing between Oxidation and Reduction
Johnny Betancourt
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3
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01:18
Distinguishing between Oxidation and Reduction
Johnny Betancourt
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4
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00:54
Distinguishing between Oxidation and Reduction
Johnny Betancourt
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더 많은 영상 (1)
Alcohol Protecting Groups
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General features of Alcohol Protecting Groups.
Johnny Betancourt
1351
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10
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Silyl Ether Protecting Groups
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Mechanism of Silyl Ether Protecting Groups.
Johnny Betancourt
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03:37
Predict the product of the following reaction.
Johnny Betancourt
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16
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9
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