Content Frame
Note for screen reader users: There is text between the form elements on this page. To be sure that you do not miss any text, use item by item navigation methods, rather than tabbing from form element to form element
[Skip Breadcrumb Navigation]

Practice Exercise 3

This activity contains 7 questions.

Question 1
1 Which statement about the C-X bond of a reactant in a nucleophilic substitution reaction is not correct?
End of Question 1

Question 2
2 Which of the following statements describes an SN2 reaction?
End of Question 2

Question 3
3 An SN2 reaction involves back side attack, which results in a "Walden Inversion." For which of the following reactants would you be able to demonstrate that back side attack occurs?
End of Question 3

Question 4
4 Which of the following alkyl halides is the least reactive in an SN2 reaction?
End of Question 4

Question 5
5 Which nucleophile is required to convert 1-bromobutane to butyl methyl ether?
End of Question 5

Question 6
6 What is the rate-determining step in the hydrolysis of tert-butyl bromide?
End of Question 6

Question 7
7 Which statement describes the difference between the reaction coordinate diagrams of SN1 and SN2 reactions?
End of Question 7

Clear Answers/Start Over

Answer choices in this exercise appear in a different order each time the page is loaded.

Copyright © 1995 - 2021 Pearson Education . All rights reserved. Pearson Prentice Hall is an imprint of Pearson .
Legal Notice | Privacy Policy | Permissions

[Return to the Top of this Page]