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Which of the following is the most reactive substrate in an E1 reaction? Which of the following is the most reactive substrate in an E1 reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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What is (are) the product(s) of the following reaction? What is (are) the product(s) of the following reaction?   A) I and II B) II and III C) I and III D) I,II,and III


A) I and II
B) II and III
C) I and III
D) I,II,and III

Correct Answer

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Which alkyl halide(s) would give the following alkene as the only product in an elimination reaction? Which alkyl halide(s) would give the following alkene as the only product in an elimination reaction?   A) Only I B) Only II C) Only III D) I and II


A) Only I
B) Only II
C) Only III
D) I and II

Correct Answer

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What is the product of the following reaction? What is the product of the following reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

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Which of the following is the least reactive substrate in an E2 reaction? Which of the following is the least reactive substrate in an E2 reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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A

Which of the labeled protons in the compound below is most readily abstracted under E2 conditions? Which of the labeled protons in the compound below is most readily abstracted under E2 conditions?   A) H<sub>a</sub> B) H<sub>b</sub> C) H<sub>c</sub> D) H<sub>d</sub>


A) Ha
B) Hb
C) Hc
D) Hd

Correct Answer

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What is the major elimination product obtained from the following reaction? What is the major elimination product obtained from the following reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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Which of the following alkyl halides would afford the indicated product upon reaction with sodium methoxide? Which of the following alkyl halides would afford the indicated product upon reaction with sodium methoxide?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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Which of the following is the major elimination product of the following reaction? Which of the following is the major elimination product of the following reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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D

What is the most likely mechanism for the reaction below? What is the most likely mechanism for the reaction below?   A) S<sub>N</sub>1 B) S<sub>N</sub>2 C) E1 D) E2


A) SN1
B) SN2
C) E1
D) E2

Correct Answer

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What is the major elimination product obtained from the following reaction? What is the major elimination product obtained from the following reaction?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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Which is the most likely mechanism for the following reaction? Which is the most likely mechanism for the following reaction?   A) S<sub>N</sub>1 B) S<sub>N</sub>2 C) E1 D) E2


A) SN1
B) SN2
C) E1
D) E2

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D

Which of the following statements about the mechanism of an E2 reaction is true?


A) All bonds are broken and formed in multiple steps.
B) The reaction is not concerted.
C) Entropy favors the reactants of an E2 reaction.
D) Entropy favors the products of an E2 reaction.

Correct Answer

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What is (are) the elimination product(s) of the following reaction? What is (are) the elimination product(s) of the following reaction?   A) Only I B) Only II C) Only III D) II and III


A) Only I
B) Only II
C) Only III
D) II and III

Correct Answer

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What is the major elimination product in the reaction of 1-bromobutane with potassium tert-butoxide in tert-butanol?


A) cis-2-Butene
B) 1-Butene
C) trans-2-Butene
D) Butanol

Correct Answer

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What is (are) the product(s) of the following reaction? What is (are) the product(s) of the following reaction?   A) Only I B) Only II C) Only III D) I and II


A) Only I
B) Only II
C) Only III
D) I and II

Correct Answer

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Which of the following statements about an E1 mechanism is not true?


A) It is a two-step process and has the same first step as an SN1 mechanism.
B) It involves the formation of a carbocation from eliminating a good leaving group.
C) A common competing reaction is rearrangement of a less stable carbocation to a more stable carbocation.
D) The loss of a proton by the carbocation is a slow step.

Correct Answer

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Which of the following is the most stable alkene? Which of the following is the most stable alkene?   A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

Correct Answer

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What is (are) the elimination product(s) of the following reaction? What is (are) the elimination product(s) of the following reaction?   A) Only I B) Only II C) Only III D) II and III


A) Only I
B) Only II
C) Only III
D) II and III

Correct Answer

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What is (are) the product(s) of the following reaction? What is (are) the product(s) of the following reaction?   A) Only I B) Only II C) Only III D) I and II


A) Only I
B) Only II
C) Only III
D) I and II

Correct Answer

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