Practice Substitution Reactions of Haloalkanes (Nucleophilic Substitution) - 10.2.2 | Chapter 10: Organic Chemistry II (Reactions & Mechanisms) | IB Grade 12-Chemistry
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Practice Questions

Test your understanding with targeted questions related to the topic.

Question 1

Easy

Define what a nucleophile is.

💡 Hint: Think of what types of species can act as electron donors.

Question 2

Easy

What does SN1 stand for?

💡 Hint: Focus on the number of steps in this mechanism.

Practice 4 more questions and get performance evaluation

Interactive Quizzes

Engage in quick quizzes to reinforce what you've learned and check your comprehension.

Question 1

What is the main difference between the SN1 and SN2 mechanisms?

  • SN1 is bimolecular and one step
  • SN2 is unimolecular and two steps.
  • SN2 is bimolecular and one step
  • SN1 is unimolecular and two steps.
  • SN1 involves inversion
  • SN2 does not.

💡 Hint: Consider the molecularity and steps of each mechanism.

Question 2

True or False: Tertiary haloalkanes favor the SN2 pathway.

  • True
  • False

💡 Hint: Think about how the structure of the haloalkane affects nucleophilic attack.

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Challenge Problems

Push your limits with challenges.

Question 1

Predict the products and identify the mechanism (SN1 or SN2) of the reaction between (CH3)3CBr and OH-.

💡 Hint: Think about the structure of the haloalkane and its stability.

Question 2

Explain why strong nucleophiles are preferred in SN2 reactions, using nucleophiles like CN− and OH− as examples.

💡 Hint: Consider what makes a nucleophile effective in substitution.

Challenge and get performance evaluation