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Quiz 1



This activity contains 15 questions.

Question 1
1 Which statement best describes a carbon-chlorine bond?
 
End of Question 1


Question 2
2 Which of the following does not affect the mechanism of a nucleophilic substitution reaction?
 
End of Question 2


Question 3
3 Which type of reactant shows the greatest reactivity in an SN2 reaction?
 
End of Question 3


Question 4
4 Which of the following represents the relative leaving group abilities of the halide ions?
 
End of Question 4


Question 5
5 Which statement best describes the mechanism of an SN2 reaction?
 
End of Question 5


Question 6
6 Which of the following is not a correct statement?
 
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Question 7
7 Which of the following compounds would be the most reactive in an SN2 reaction?
 
End of Question 7


Question 8
8 Which of the following is the rate law for an SN1 reaction?
 
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Question 9
9 Which of the following is the rate-limiting step for the hydrolysis of tert-butyl bromide?
 
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Question 10
10 Which of the following alkyl bromides is the most reactive in an SN1 reaction?
 
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Question 11
11 Which of the following describes the reaction coordinate diagram for the hydrolysis of tert-butyl bromide to a neutral alcohol?
 
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Question 12
12 Which of the following is the most nucleophilic towards CH3I?
 
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Question 13
13 What product(s) will be formed from an E2 reaction of 2-bromopentane and ethoxide ion in ethanol?
 
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Question 14
14 Suppose you have an alkyl halide that can undergo both E1 and E2 reactions with methoxide ion. What steps can you take to increase the percentage of the reaction that takes place by the E2 pathway?
 
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Question 15
15 Which of the following statements does not apply to the reaction coordinate diagram for an E2 reaction of 2-bromobutane?
 
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