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Alcohols: Reduction, Oxidation, Grignard Reactions, and Protecting Groups

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Grignard Reaction

  • Reactions of Organometallics
    13:40

Leaving Group Conversions - Using HX

  • Why do we need to convert Alcohol into a good leaving group?
    02:03
  • Using HX acids via SN2 reaction.
    02:16
  • Using HX acids via SN1 reaction.
    07:20

Leaving Group Conversions - SOCl2 and PBr3

  • Predict the mechanism of PBr3, and draw the final product.
    06:01
  • Learning the mechanism of SOCl2.
    07:18

Dehydration Reaction

  • Dehydration of 1° alcohols:The E2 Mechanism
    05:20
  • An extra note of caution with 1° alcohols.
    01:06
  • General features of acid-catalyzed dehydration.
    06:01

POCl3 Dehydration

  • Mechanism of Dehydration with POCl3
    04:52
  • General Reaction of Dehydration with POCl3
    01:23

Oxidizing and Reducing Agents

  • Distinguishing between Oxidation and Reduction
    00:54
  • Distinguishing between Oxidation and Reduction
    01:18
  • Distinguishing between Oxidation and Reduction
    00:54

Alcohol Protecting Groups

  • General features of Alcohol Protecting Groups.
    03:01

Silyl Ether Protecting Groups

  • Mechanism of Silyl Ether Protecting Groups.
    07:16
  • Predict the product of the following reaction.
    03:37