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Spectroscopy, Structure Elucidation, and Functional Group Transformations in Organic Chemistry

주석실무비디오 수업

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Mass Spectrometry

  • Equipment and Theory
    10:48
  • How to Read a Mass Spectrum
    01:25

Mass Spect:Isotopes

  • The (M + 1) Peak
    09:26
  • The Nitrogen Rule
    03:32
  • The (M + 2) Peak
    05:23

Infrared Spectroscopy

  • General Features of IR Spect
    16:04

NMR Spectroscopy

  • General NMR Features
    10:06

1H NMR:Spin-Splitting (N + 1) Rule

  • Splitting without J-values
    12:21
  • Proton Splitting
    03:

NMR Integration

  • 1H NMR Integration
    06:46
  • Draw Complete NMR Spectrum
    04:29

UV-Vis Spectroscopy of Conjugated Alkenes

  • 가이드 코스
    UV-Vis Spectroscopy of Conjugated Alkenes Concept 1
    1:56
  • 가이드 코스
    UV-Vis Spectroscopy of Conjugated Alkenes Example 1
    1:33
  • 가이드 코스
    UV-Vis Spectroscopy of Conjugated Alkenes Concept 2
    3:17

Diels-Alder Reaction

  • General Features
    09:48

Naming Benzene Rings

  • Benzene Nomenclature
    09:04

Benzyne

  • Regiospecificity
    03:20
  • General Mechanism
    06:06
  • Activating and deactivating groups
    03:27

Markovnikov

  • Provide the mechanism
    01:26
  • How to add to asymmetrical double bonds.
    03:38

Oxymercuration

  • Acid-catalyzed oxymercuration-reduction mechanism
    09:01
  • General properties of oxymercuration-reduction.
    05:

Hydroboration

  • General properties of hydroboration-oxidation.
    06:38
  • Acid-catalyzed hydroboration-oxidation mechanism
    06:14

Dihydroxylation

  • General properties of syn vicinal dihydroxylation.
    03:50
  • Predict the product for the following multi-step reaction.
    04:42

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

Naming Alcohols

  • How to name alcohols
    01:01
  • Name the following compound
    03:59
  • Old school vs. new school naming
    03:03

Epoxide Reactions

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

Nucleophilic Addition

  • Nucleophilic Addition
    08:27