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]

Quiz 2



This activity contains 13 questions.

Question 1
1 Which of the following is not a contributing resonance structure for CH2=CH-CH=CH-.CH2?
 
End of Question 1


Question 2
2 How many different products could be obtained in the reaction of CH2=CH-CH=CH-CH2+-CH3 with a bromide ion?
 
End of Question 2


Question 3
3 Which of the following compounds is the most stable?
 
End of Question 3


Question 4
4 What carbon is protonated in the first step of the reaction of 3-methyl-2,4-heptadiene with one equiv of HBr?
 
End of Question 4


Question 5
5 What kind of reactions do dienes most commonly undergo?
 
End of Question 5


Question 6
6 Which statement describes how a UV/Vis spectrum is affected by increasing the number of conjugated double bonds in a compound?
 
End of Question 6


Question 7
7 Which of the following compounds is the most stable?
 
End of Question 7


Question 8
8 Which of the following compounds has the UV spectrum with the greatest lambda max?
 
End of Question 8


Question 9
9 Which of the following is not a rule for drawing resonance contributors?
 
End of Question 9


Question 10
10 Which of the following would be most reactive toward electrophilic addition of HBr?
 
End of Question 10


Question 11
11 How many resonance contributors does the anilinium ion, C6H5-(+)NH3, have?
 
End of Question 11


Question 12
12 Which of the following is the most stable resonance contributor of N2O?
 
End of Question 12


Question 13
13 Which compound contains the oxygen atom with the greatest electron density?
 
End of Question 13


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]