Deck 8: Alkyl Halides and Elimination Reactions
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Deck 8: Alkyl Halides and Elimination Reactions
1
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
A)cis-2-Butene
B)1-Butene
C)trans-2-Butene
D)Butanol
1-Butene
2
Which of the following is the most reactive substrate in an E2 reaction?

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

A)I
B)II
C)III
D)IV
IV
3
Which of the following statements about an E1 mechanism is not true?
A)The reaction is fastest with tertiary alkyl halides.
B)A better leaving group makes the reaction rate increase.
C)The reaction follows first-order kinetics.
D)Stronger bases favor the E1 reaction.
A)The reaction is fastest with tertiary alkyl halides.
B)A better leaving group makes the reaction rate increase.
C)The reaction follows first-order kinetics.
D)Stronger bases favor the E1 reaction.
Stronger bases favor the E1 reaction.
4
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
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5
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
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6
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
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7
What is the major 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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8
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
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9
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.
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.
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10
Which of the following is the major E2 product formed from the following alkyl halide?

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

A)I
B)II
C)III
D)IV
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11
Which of the following statements about an E1 mechanism is true?
A)The identity of the leaving group affects the rate of reaction.
B)The reaction follows second-order kinetics.
C)The reaction is slowest with tertiary substrates.
D)Polar aprotic solvents favor the E1 mechanism.
A)The identity of the leaving group affects the rate of reaction.
B)The reaction follows second-order kinetics.
C)The reaction is slowest with tertiary substrates.
D)Polar aprotic solvents favor the E1 mechanism.
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12
Which of the labeled protons in the compound below is most readily abstracted under E2 conditions?

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

A)Ha
B)Hb
C)Hc
D)Hd
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13
How many different E2 products can form from the dehydrohalogenation of 2-bromobutane?
A)1
B)2
C)3
D)4
A)1
B)2
C)3
D)4
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14
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
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15
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
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16
Which of the following statements about the mechanism of an E2 reaction is not true?
A)It is fastest with tertiary halides.
B)It exhibits first-order kinetics.
C)A better leaving group should make a faster reaction.
D)All bonds are broken and formed in a single step.
A)It is fastest with tertiary halides.
B)It exhibits first-order kinetics.
C)A better leaving group should make a faster reaction.
D)All bonds are broken and formed in a single step.
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17
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.
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.
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18
Classify each alkene in vitamin D3 labeled I, II, III by the number of carbon substituents bonded to the double bond. 
A)I = Disubstituted; II = trisubstituted; III = trisubstituted.
B)I = Monosubstituted; II = disubstituted; III = trisubstituted.
C)I = Disubstituted; II = disubstituted; III = trisubstituted.
D)I = Disubstituted; II = trisubstituted; III = disubstituted.

A)I = Disubstituted; II = trisubstituted; III = trisubstituted.
B)I = Monosubstituted; II = disubstituted; III = trisubstituted.
C)I = Disubstituted; II = disubstituted; III = trisubstituted.
D)I = Disubstituted; II = trisubstituted; III = disubstituted.
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19
Which of the following represents the rate law for an E2 reaction?
A)Rate = k[alkyl halide]
B)Rate = k[alkyl halide][base]
C)Rate = k[alkyl halide]2
D)Rate = k[base]2
A)Rate = k[alkyl halide]
B)Rate = k[alkyl halide][base]
C)Rate = k[alkyl halide]2
D)Rate = k[base]2
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20
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
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21
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
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22
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
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23
What is the product 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
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24
What is the most likely mechanism for the reaction below?

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

A)SN1
B)SN2
C)E1
D)E2
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25
What is (are) the 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
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26
Which of the following alkyl halides will afford the product below as the major product in an E2 reaction?

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

A)I
B)II
C)III
D)IV
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27
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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28
Consider the following E2 reaction.What rate equation would be observed for this reaction?
![<strong>Consider the following E2 reaction.What rate equation would be observed for this reaction? </strong> A)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br] B)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br][KOC(CH<sub>3</sub>)<sub>3</sub>] C)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br][KOC(CH<sub>3</sub>)<sub>3</sub>]<sup>2</sup> D)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br]<sup>2</sup>[KOC(CH<sub>3</sub>)<sub>3</sub>]](https://d2lvgg3v3hfg70.cloudfront.net/TB5872/11eb4ad7_6bf8_22ce_99b2_23a4a4e78d70_TB5872_00.jpg)
A)Rate = k[CH3CH2CH2Br]
B)Rate = k[CH3CH2CH2Br][KOC(CH3)3]
C)Rate = k[CH3CH2CH2Br][KOC(CH3)3]2
D)Rate = k[CH3CH2CH2Br]2[KOC(CH3)3]
![<strong>Consider the following E2 reaction.What rate equation would be observed for this reaction? </strong> A)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br] B)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br][KOC(CH<sub>3</sub>)<sub>3</sub>] C)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br][KOC(CH<sub>3</sub>)<sub>3</sub>]<sup>2</sup> D)Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>Br]<sup>2</sup>[KOC(CH<sub>3</sub>)<sub>3</sub>]](https://d2lvgg3v3hfg70.cloudfront.net/TB5872/11eb4ad7_6bf8_22ce_99b2_23a4a4e78d70_TB5872_00.jpg)
A)Rate = k[CH3CH2CH2Br]
B)Rate = k[CH3CH2CH2Br][KOC(CH3)3]
C)Rate = k[CH3CH2CH2Br][KOC(CH3)3]2
D)Rate = k[CH3CH2CH2Br]2[KOC(CH3)3]
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29
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
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30
Which of the following is the dihalide that can be used to prepare the alkyne below?

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
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31
Which of the following is most likely to react as a nucleophile rather than a base?

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

A)I
B)II
C)III
D)IV
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32
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
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33
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
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34
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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35
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
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36
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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37
What is the most likely mechanism for the reaction below?

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

A)SN1
B)SN2
C)E1
D)E2
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38
Select the elimination product(s) formed by treating the indicated alkyl halide with a base. 
A)Only I
B)Only II
C)Only III
D)I, II, and III

A)Only I
B)Only II
C)Only III
D)I, II, and III
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39
What is (are) the starting material(s) in the reaction below?

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
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40
Which of the following is the dihalide that can be used to prepare the alkyne below?

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
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41
Which of the following alkenes is the most stable?

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

A)I
B)II
C)III
D)IV
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42
Which of the following alkyl chloride affords alkene A exclusively under E2 reaction condition?

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

A)I
B)II
C)III
D)IV
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43
Which of the following alkyl halide reacts the fastest in an E2 reaction?

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

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