Electrophilic Aromatic Substitution Reactivity
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Questions and Answers

Which type of group donates electron density into a conjugated π system via resonance or inductive effects, making the π system more nucleophilic?

  • Electron withdrawing group (EWG)
  • Electron donating group (EDG) (correct)
  • Electron releasing group (ERG)
  • Electron activating group (EAG)
  • What effect does an electron withdrawing group (EWG) have on the nucleophilicity of the aromatic ring?

  • It stabilizes the nucleophilicity
  • It increases the nucleophilicity
  • It decreases the nucleophilicity (correct)
  • It has no effect on the nucleophilicity
  • What is the effect of steric effects on the activating groups in electrophilic aromatic substitution reactions?

  • They interfere with the activating effect (correct)
  • They enhance the activating effect
  • They have no effect on the activating groups
  • They stabilize the activating effect
  • Which property is important in determining the positions on the aromatic ring where substitution reactions are most likely to take place?

    <p>Relative position of substituent groups</p> Signup and view all the answers

    What does an electron releasing group do to an aromatic ring for electrophilic substitution reactions?

    <p>Increases its reactivity</p> Signup and view all the answers

    Study Notes

    Activating and Deactivating Groups in Electrophilic Aromatic Substitution

    • Electron donating groups (EDGs) donate electron density into a conjugated π system via resonance or inductive effects, making the π system more nucleophilic.

    Electron Withdrawing Groups (EWGs)

    • EWGs decrease the nucleophilicity of the aromatic ring, making it less reactive.

    Steric Effects

    • Steric effects hinder the approach of electrophiles to the aromatic ring, reducing the reactivity of the activating groups.

    Substitution Reactions

    • The distribution of electron density in the aromatic ring is important in determining the positions where substitution reactions are most likely to take place.

    Electron Releasing Groups (ERGs)

    • ERGs increase the electron density of the aromatic ring, making it more reactive towards electrophiles and favouring electrophilic substitution reactions.

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    Description

    Test your knowledge on how existing substituent groups on an aromatic ring influence reaction rates and product formation in electrophilic aromatic substitution reactions.

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