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Ethers, Epoxides, and Thioethers: Structure, Properties, and Reactions

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Functional Groups

  • Assigning Degrees to Alkyl Halides
    01:30
  • Why we need functional groups.
    01:49
  • The difference between aldehydes and ketones.
    03:08

Naming Ethers

  • 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

Naming Epoxides

  • How to name cyclic ethers using the cycloalkane convention.
    03:23
  • How to name epoxides using the epoxy convention.
    01:20
  • Defining what an epoxide (oxirane) is.
    01:09

Williamson Ether Synthesis

  • The Mechanism of Williamson Ether Synthesis.
    03:50

Ether Cleavage

  • How to predict the products of Ether Cleavage.
    04:22
  • Predict the product of the following reaction.
    03:44

Intermolecular Forces

  • How dipole-dipole forces work.
    01:46
  • How IMFs are related to melting and boiling points.
    03:08
  • How Van der Waals forces work.
    03:01

Solubility

  • Introducing common solvents and other molecules in organic chemistry.
    02:01
  • Understanding “like dissolves like”.
    01:47

Grignard Reaction

  • Reactions of Organometallics
    13:40

Epoxidation

  • Halohydrins to epoxides via intramolecular SN2.
    02:26
  • General properties of epoxidation.
    02:19
  • The mechanism of how peroxy acids make epoxides.
    03:19

Epoxide Reactions

  • Base-Catalyzed Epoxide Ring-Opening
    04:44
  • Acid-Catalyzed Epoxide Ring-Opening
    04:34

Halohydrin

  • Halohydrin Mechanism
    04:48
  • General properties of halohydrin formation.
    01:44

Silyl Ether Protecting Groups

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

Thiol Reactions

  • The mechanism of Disulfide Synthesis.
    02:55
  • The mechanism of Sulfide Synthesis.
    03:21