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Organic Chemistry II Exam 2 Practice – Step-by-Step Guidance

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Intro to Redox

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

Aldehyde Via Reducing Agents

  • LiAl(ot-Bu)3H on Acid Chlorides
    01:42
  • Why LiAlH4 doesn't work
    02:07
  • DIBAL-H on Esters and Nitriles
    02:10

Reactions of Organometallics

  • Reactions of Organometallics
    13:40

Preparation of Organometallics

  • Ruining Organometallics
    02:50
  • General Reaction
    12:21

Nucleophilic Addition

  • Nucleophilic Addition
    08:27

Ketones from Acid Chlorides

  • Ketones from acid chlorides
    05:26

Factors Affecting Acidity

  • Which of the oxides is the most basic?
    00:30
  • The 3 factors that determine the strength of inductive effects.
    03:09
  • Using Inductive Effect to determine acidity
    01:54

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

Leaving Groups

  • The 3 important leaving groups to know.
    07:22