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Organic Chemistry Study Guide: Synthesis, Mechanisms, and Nomenclature

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Alkane Nomenclature

  • Naming the root chain
    01:02
  • Provide the IUPAC name for the following alkane
    07:08
  • The different parts of an IUPAC name
    03:43

Ether Nomenclature

  • How to name ethers using the IUPAC naming system.
    02:08
  • How to name ethers using the common naming system.
    01:32
  • Provide the correct common name of the following ether.
    01:22

Synthesis of Alcohols Overview

  • Forming alcohols through SN2 reactions.
    01:44
  • Forming alcohols through Acid-Catalyzed Hydration.
    02:02
  • Forming alcohols through Hydroboration-Oxidation.
    01:37

Reaction Mechanism

  • How to tell if charged molecules will react as nucleophiles or electrophiles.
    02:39
  • Nucleophile or Electrophile
    01:49
  • How to tell if uncharged molecules will react as nucleophiles or electrophiles.
    02:48

Overview of Chemical Reactions

  • Recognizing Substitution Reactions.
    01:34
  • Recognizing Acid-Base Reactions.
    02:43
  • Recognizing Elimination Reactions.
    00:40

Alkyl Groups

  • Name the following alkane
    02:33
  • Understanding Non-IUPAC Substituents
    06:42
  • Name the following alkane
    03:56

Introduction to Substitution

  • Predict the product
    05:55
  • Nucleophiles and Electrophiles can react in Bronsted-Lowry Reactions.
    05:01
  • Nucleophiles and Electrophiles can react in Substitution Reactions.
    01:47

The SN2 Mechanism

  • Ranking reactivity toward SN2
    04:03
  • Drawing the SN2 Mechanism
    08:33
  • Understanding the properties of SN2.
    11:57

SN1 Mechanism

  • Drawing the SN1 Mechanism
    10:49
  • Why highly substituted leaving groups favor SN1.
    01:13
  • Understanding the properties of SN1.
    08:16

Leaving Groups

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

Alkene Metathesis

  • Percorso guidato
    Alkene Metathesis Example 1
    1:47
  • Percorso guidato
    Alkene Metathesis Example 4
    1:41
  • Percorso guidato
    Alkene Metathesis Example 2
    3:04

Sharpless Asymmetric Epoxidation

  • General reaction of Sharpless Epoxidation.
    01:37
  • How to draw and predict a Sharpless Epoxidation.
    03:33
  • Important Reagents of Sharpless Epoxidation.
    04:39

Alcohol Protecting Groups

  • General features of Alcohol Protecting Groups.
    03:01

Organometallics

  • Nucleophilic Addition on Ketones and Aldehydes
    03:57
  • Organometallic on Aldehyde
    03:21

Reactions of Organometallics

  • Reactions of Organometallics
    13:40