JoVE Logo

Meld u aan

Nucleophilic Substitution

Overzicht

Source: Vy M. Dong and Daniel Kim, Department of Chemistry, University of California, Irvine, CA

Nucleophilic substitution reactions are among the most fundamental topics covered in organic chemistry. A nucleophilic substitution reaction is one where a nucleophile (electron-rich Lewis base) replaces a leaving group from a carbon atom.

SN1 (S = Substitution, N = Nucleophilic, 1 = first-order kinetics)
SN2 (S = Substitution, N = Nucleophilic, 2 = second-order kinetics)

This video will help to visualize the subtle differences between an SN1 and SN2 reaction and what factors help to speed up each type of nucleophilic substitution reaction. The first section will focus on reactions that will help to better understand and learn about nucleophilic substitution reactions. The second section will focus on a real-world example of a substitution reaction.

Procedure

Part 1: Studying SN1 Reactions

Alkyl Halide Structure:

  1. Measure 2 mL of a 0.1 M solution of silver nitrate in absolute ethanol into each of the three test tubes.
  2. Add 2 drops of 1-bromobutane into the first test tube. Add 2 drops of 2-bromobutane into the second test tube.
  3. Add 2 drops of 2-bromo-2-methylpropane into the final, third test tube.
  4. Stopper and shake each test tube.
  5. Note the time at which the first signs of cloudiness or pre

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Resultaten

Part 1: Studying SN1 Reactions

Alkyl Halide Structure:

Figure 9

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Toepassing en samenvatting

These experiments are designed to quickly show trends in nucleophilic substitution reactions. Experimentally testing these trends helps to better understand the subtle differences between an SN1 and SN2 reaction. Chemists have learned to develop and optimize reaction conditions. It all stems from first understanding the reaction: what speeds up or slows down a reaction and how can we take advantage of it? Choosing the best solvent, temperature, or concentration of reagents can greatly affect how fas

Log in or to access full content. Learn more about your institution’s access to JoVE content here

Tags

Nucleophilic SubstitutionOrganic SynthesisElectron rich SpeciesAlkyl HalideFunctional GroupReactantsFunctionalized AlkaneAlcoholSulfonic HalideAlkyl HalideAlpha CarbonBeta CarbonElectrophileNucleophileChloride IonAcetate Ion

Ga naar...

0:00

Overview

0:45

Principles of Nucleophilic Substitution

4:00

SN1 Reaction

6:11

Results: Rate of SN1 Reactions

8:32

SN2 Reactions

10:03

Results: Rates of SN2 Reactions

12:45

Applications

Video's uit deze collectie:

article

Now Playing

Nucleophilic Substitution

Organic Chemistry II

99.6K weergaven

article

Cleaning Glassware

Organic Chemistry II

123.9K weergaven

article

Reducing Agents

Organic Chemistry II

43.2K weergaven

article

Grignard Reaction

Organic Chemistry II

149.3K weergaven

article

n-Butyllithium Titration

Organic Chemistry II

48.1K weergaven

article

Dean-Stark Trap

Organic Chemistry II

100.7K weergaven

article

Ozonolysis of Alkenes

Organic Chemistry II

67.2K weergaven

article

Organocatalysis

Organic Chemistry II

17.0K weergaven

article

Palladium-Catalyzed Cross Coupling

Organic Chemistry II

34.7K weergaven

article

Solid Phase Synthesis

Organic Chemistry II

41.3K weergaven

article

Hydrogenation

Organic Chemistry II

49.7K weergaven

article

Polymerization

Organic Chemistry II

94.9K weergaven

article

Melting Point

Organic Chemistry II

150.1K weergaven

article

Infrared Spectroscopy

Organic Chemistry II

216.2K weergaven

article

Polarimeter

Organic Chemistry II

100.3K weergaven

JoVE Logo

Privacy

Gebruiksvoorwaarden

Beleid

Onderzoek

Onderwijs

Over JoVE

Auteursrecht © 2025 MyJoVE Corporation. Alle rechten voorbehouden