Deck 7: Alkyl Halides: Nucleophilic Substitution and Elimination Reactions
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Deck 7: Alkyl Halides: Nucleophilic Substitution and Elimination Reactions
1
Which of the following is a primary alkyl halide?
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
(CH3)2CHCH2Cl
2
What is the IUPAC name for the following compound? 
A) 2-Bromo-4-pentylhexane
B) (2S,4S)-2-Bromo-4,5-diethylheptane
C) 3,4-Diethyl-6-bromoheptane
D) 2-Bromo-4-methylhexane
E) (2R,4R)-2-Bromo-4,5-diethylheptane

A) 2-Bromo-4-pentylhexane
B) (2S,4S)-2-Bromo-4,5-diethylheptane
C) 3,4-Diethyl-6-bromoheptane
D) 2-Bromo-4-methylhexane
E) (2R,4R)-2-Bromo-4,5-diethylheptane
(2S,4S)-2-Bromo-4,5-diethylheptane
3
For the following reaction, label the nucleophile, electrophile, and leaving group. 


4
What is the nucleophile in 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 nucleophile in the following reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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6
Which of the following is a substitution reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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7
Which of the following is an elimination 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 an elimination 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 is a tertiary alkyl halide?
A) 1-Bromo-2-methylpropane
B) 2-Bromopropane
C) 1-Bromobutane
D) 2-Bromo-2-methylpropane
A) 1-Bromo-2-methylpropane
B) 2-Bromopropane
C) 1-Bromobutane
D) 2-Bromo-2-methylpropane
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10
Which of the following is a secondary alkyl halide?
A) 1-Bromo-2-methylpropane
B) 2-Bromopropane
C) 1-Bromobutane
D) 2-Bromo-2-methylpropane
A) 1-Bromo-2-methylpropane
B) 2-Bromopropane
C) 1-Bromobutane
D) 2-Bromo-2-methylpropane
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11
What is the electrophile in the following reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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12
What is the electrophile in the following reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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13
Which of the following is a tertiary alkyl halide?
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CHClCH2CH3
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CHClCH2CH3
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14
What is the IUPAC name for the following compound? 
A) Chlorocyclopentane
B) 2-Chloro-1-methylcyclopentane
C) 1-Methyl-2-chlorocyclopentane
D) 1-Chloro-2-methylcyclopentane

A) Chlorocyclopentane
B) 2-Chloro-1-methylcyclopentane
C) 1-Methyl-2-chlorocyclopentane
D) 1-Chloro-2-methylcyclopentane
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15
Which of the following is a substitution reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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16
What is the IUPAC name for the following compound? 
A) 3-Fluorobutane
B) 2-Fluorobutane
C) (S)-2-Fluorobutane
D) (R)-2-Fluorobutane

A) 3-Fluorobutane
B) 2-Fluorobutane
C) (S)-2-Fluorobutane
D) (R)-2-Fluorobutane
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17
For the following reaction, label the nucleophile, electrophile, and leaving group. 

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18
Which of the following is a substitution reaction? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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19
Which of the following is a secondary alkyl halide?
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
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20
What is the classification for the following halide? 
A) primary halide
B) secondary halide
C) tertiary halide
D) quaternary halide

A) primary halide
B) secondary halide
C) tertiary halide
D) quaternary halide
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21
Provide the structure for (4R,8S)-4-iodo-2,2,8-trimethyldecane.
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22
When drawing a curved arrow mechanism, the tail of the arrow starts at______.
A) the bond that is being formed
B) the atom with the positive charge
C) the source of electrons that is being moved
D) the location to which the electrons are being moved
A) the bond that is being formed
B) the atom with the positive charge
C) the source of electrons that is being moved
D) the location to which the electrons are being moved
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23
What is the IUPAC name for the following compound? 

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24
Consider the following SN2 reaction,
Assuming no other changes, what is the effect on the rate, if the concentration of 2-bromopentane is doubled and the concentration of CH3CH2COONa is halved?
A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half

A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half
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25
Consider the following SN2 reaction,
Assuming no other changes, what is the effect on the rate, if the concentration of both 1-chloro-3-methylbutane and NaN3 is doubled?
A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half

A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half
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26
Which of the following is the rate equation for the following reaction? ![<strong>Which of the following is the rate equation for the following reaction? </strong> A) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>] B) Rate = k[NaN<sub>3</sub>] C) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>] [NaBr] D) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>]<sup> </sup>[NaN<sub>3</sub>] E) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>]<sup>2 </sup>[NaN<sub>3</sub>]](https://storage.examlex.com/TB4454/11ea894b_ac90_45bf_bba7_8f3ec231a858_TB4454_00_TB4454_00.jpg)
A) Rate = k[CH3CH2CH2CHBrCH3]
B) Rate = k[NaN3]
C) Rate = k[CH3CH2CH2CHBrCH3] [NaBr]
D) Rate = k[CH3CH2CH2CHBrCH3] [NaN3]
E) Rate = k[CH3CH2CH2CHBrCH3]2 [NaN3]
![<strong>Which of the following is the rate equation for the following reaction? </strong> A) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>] B) Rate = k[NaN<sub>3</sub>] C) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>] [NaBr] D) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>]<sup> </sup>[NaN<sub>3</sub>] E) Rate = k[CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CHBrCH<sub>3</sub>]<sup>2 </sup>[NaN<sub>3</sub>]](https://storage.examlex.com/TB4454/11ea894b_ac90_45bf_bba7_8f3ec231a858_TB4454_00_TB4454_00.jpg)
A) Rate = k[CH3CH2CH2CHBrCH3]
B) Rate = k[NaN3]
C) Rate = k[CH3CH2CH2CHBrCH3] [NaBr]
D) Rate = k[CH3CH2CH2CHBrCH3] [NaN3]
E) Rate = k[CH3CH2CH2CHBrCH3]2 [NaN3]
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27
Which of the following is a reasonable definition of a concerted reaction?
A) a reaction in which bond breaking occurs first
B) a reaction in which all bond-breaking and bond-forming occurs at the same time
C) a reaction in which bond forming occurs first
D) a substitution reaction
A) a reaction in which bond breaking occurs first
B) a reaction in which all bond-breaking and bond-forming occurs at the same time
C) a reaction in which bond forming occurs first
D) a substitution reaction
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28
What is the IUPAC name for the following compound? 

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29
What is the correct structure for 2-bromo-3-methylbutane? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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30
What is the IUPAC name for the following compound? 
A) 1,2-bromocyclopentane
B) (1R, 2S)-1,2-dibromocyclopentane
C) (1S, 2S)-1,2-dibromocyclopentane
D) (1S, 2R)-1,2-dibromocyclopentane
E) (1R, 2R)-1,2-dibromocyclopentane

A) 1,2-bromocyclopentane
B) (1R, 2S)-1,2-dibromocyclopentane
C) (1S, 2S)-1,2-dibromocyclopentane
D) (1S, 2R)-1,2-dibromocyclopentane
E) (1R, 2R)-1,2-dibromocyclopentane
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31
What is the IUPAC name for the following compound? 

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32
Provide the structure for 1-chloro-4-isopropylheptane.
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33
When drawing a curved arrow mechanism, the head of the arrow goes to__________.
A) the bond that is being formed
B) the bond that is being broken
C) the source of electrons that is being moved
D) the location to which the electrons are being moved
A) the bond that is being formed
B) the bond that is being broken
C) the source of electrons that is being moved
D) the location to which the electrons are being moved
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34
Consider the following SN2 reaction,
Assuming no other changes, what is the effect on the rate, if the concentration of NaN3 is tripled?
A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would increase the rate six times

A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would increase the rate six times
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35
What is the correct structure for (2S,5R)-2-fluoro-5-methylnonane? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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36
Consider the following SN2 reaction,
Assuming no other changes, what is the effect on the rate, if the concentration of 1-chloro-3-methylbutane is doubled?
A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half

A) No effect
B) It would double the rate
C) It would triple the rate
D) It would increase four times
E) It would reduce by half
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37
Which of the following is the rate equation for the following SN2 reaction? ![<strong>Which of the following is the rate equation for the following S<sub>N</sub>2 reaction? </strong> A) Rate = k[1-bromopropane] B) Rate = k[NaCN] C) Rate = k[1-bromopropane] [NaCN] D) Rate = k[1-bromopropane]<sup>2</sup> E) Rate = k[1-bromopropane]<sup>2 </sup>[NaCN]<sup>2</sup>](https://storage.examlex.com/TB4454/11ea894b_ac90_45be_bba7_8d20fe8b01be_TB4454_00_TB4454_00.jpg)
A) Rate = k[1-bromopropane]
B) Rate = k[NaCN]
C) Rate = k[1-bromopropane] [NaCN]
D) Rate = k[1-bromopropane]2
E) Rate = k[1-bromopropane]2 [NaCN]2
![<strong>Which of the following is the rate equation for the following S<sub>N</sub>2 reaction? </strong> A) Rate = k[1-bromopropane] B) Rate = k[NaCN] C) Rate = k[1-bromopropane] [NaCN] D) Rate = k[1-bromopropane]<sup>2</sup> E) Rate = k[1-bromopropane]<sup>2 </sup>[NaCN]<sup>2</sup>](https://storage.examlex.com/TB4454/11ea894b_ac90_45be_bba7_8d20fe8b01be_TB4454_00_TB4454_00.jpg)
A) Rate = k[1-bromopropane]
B) Rate = k[NaCN]
C) Rate = k[1-bromopropane] [NaCN]
D) Rate = k[1-bromopropane]2
E) Rate = k[1-bromopropane]2 [NaCN]2
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38
Provide a curved arrow mechanism for the following SN2 reaction 

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39
What is the correct structure for 3-ethyl-1-iodocyclohexane? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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40
Provide the structure for cis-1,2-dibromocyclopentane.
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41
Predict the product for the following SN2 reaction.

A) I
B) II
C) III
D) IV
E) None of these


A) I
B) II
C) III
D) IV
E) None of these
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42
Draw the transition state for the following SN2 reaction.

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 halides will undergo the fastest SN2 reaction? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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44
Draw the transition state for the following SN2 reaction.

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


A) I
B) II
C) III
D) IV
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45
Predict the product for the following SN2 reaction.

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


A) I
B) II
C) III
D) IV
E) V
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46
Rank the following compounds from most to least reactive in an SN2 reaction. 
A) I > IV > II > III
B) II > I > IV > III
C) III > IV > I > II
D) IV > I > II > III
E) IV > III > I > II

A) I > IV > II > III
B) II > I > IV > III
C) III > IV > I > II
D) IV > I > II > III
E) IV > III > I > II
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47
Which of the following is a mechanism for an SN2 reaction? 
A) I
B) II
C) III
D) IV
E) Both I & II

A) I
B) II
C) III
D) IV
E) Both I & II
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48
Provide a curved arrow mechanism and predict the product for the following SN2 reaction. 

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49
Predict the product for the following reaction.
(1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN3

(1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN3

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50
Draw the transition state for the following reaction.
(S)-1-iodo-3-methylpentane + NaSCH3
(S)-1-iodo-3-methylpentane + NaSCH3
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51
Predict the product for the following reaction.

A) I
B) II
C) III
D) IV
E) None of these


A) I
B) II
C) III
D) IV
E) None of these
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52
Which of the following alkyl halides will undergo the slowest SN2 reaction? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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53
Predict the product for the following reaction.

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


A) I
B) II
C) III
D) IV
E) V
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54
Draw the potential energy diagram for the following SN2 reaction.

A) I
B) II
C) III
D) IV
E) None of the above


A) I
B) II
C) III
D) IV
E) None of the above
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55
Predict the product for the following reaction. 

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56
Rank the following compounds from most to least reactive in an SN2 reaction. 
A) I > IV > II > III
B) II > I > IV > III
C) III > IV > I > II
D) I > III > II > IV
E) IV > III > I > II

A) I > IV > II > III
B) II > I > IV > III
C) III > IV > I > II
D) I > III > II > IV
E) IV > III > I > II
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57
Which of the following alkyl halides is essentially unreactive in an SN2 reaction? 
A) I
B) II
C) III
D) IV
E) V

A) I
B) II
C) III
D) IV
E) V
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58
Provide a curved arrow mechanism and predict the product for the following reaction. 

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59
Predict the product for the following SN2 reaction.

A) I
B) II
C) III
D) IV
E) None of these


A) I
B) II
C) III
D) IV
E) None of these
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60
Predict the product for the following SN2 reaction. 
A) I
B) II
C) III
D) IV
E) Both I & II

A) I
B) II
C) III
D) IV
E) Both I & II
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61
Predict the product for the following SN2 reaction.

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


A) I
B) II
C) III
D) IV
E) V
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62
Identify the IUPAC name for the following compound. 
A) 1-methyl-2-cyclohexene
B) 2-methylcyclohexene
C) 3-methylcyclohexene
D) 1-methyl-5-cyclohexene

A) 1-methyl-2-cyclohexene
B) 2-methylcyclohexene
C) 3-methylcyclohexene
D) 1-methyl-5-cyclohexene
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63
Identify the methylating agent used in biological systems.
A) methyl iodide
B) S-adenosylmethionine
C) methylalanine
D) methylproline
E) methyl bromide
A) methyl iodide
B) S-adenosylmethionine
C) methylalanine
D) methylproline
E) methyl bromide
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64
Which of the following is a protic solvent? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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65
Describe a strong nucleophile.
A) an anion
B) a cation
C) a radical
D) a neutral compound
A) an anion
B) a cation
C) a radical
D) a neutral compound
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66
Which of the following is NOT a nucleophile?
A) OH-
B) NH3
C) CH3OH
D) NH4+
E) All of these
A) OH-
B) NH3
C) CH3OH
D) NH4+
E) All of these
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67
Which of the following is a strong nucleophile?
A) OH-
B) H2O
C) CH3OH
D) NH4+
E) All of these
A) OH-
B) H2O
C) CH3OH
D) NH4+
E) All of these
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68
Which of the following is a weak nucleophile?
A) OH-
B) H2O
C) CH3O-
D) NH4+
E) All of these
A) OH-
B) H2O
C) CH3O-
D) NH4+
E) All of these
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69
Identify which of the following that is NOT an effect of adrenaline.
A) increases heart rate
B) elevates sugar level
C) provides boost of energy
D) increases level of oxygen
E) makes one sleepy
A) increases heart rate
B) elevates sugar level
C) provides boost of energy
D) increases level of oxygen
E) makes one sleepy
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70
Provide an IUPAC name for the following compound. 

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71
Which of the following is the IUPAC name for the following compound? 
A) 2-ethyl-1,1,3-trimethylbutene
B) 3-ethyl-2,4-dimethyl-2-pentene
C) 2,4-dimethylhexene
D) 4-ethyl-1,3-dimethyl-3-pentene

A) 2-ethyl-1,1,3-trimethylbutene
B) 3-ethyl-2,4-dimethyl-2-pentene
C) 2,4-dimethylhexene
D) 4-ethyl-1,3-dimethyl-3-pentene
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72
Predict the product for the following SN2 reaction. 

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73
Which of the following shows a mechanism of a concerted elimination? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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74
Predict the SN2 product and provide a curved arrow mechanism for the formation of the product. 

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75
What set of reaction conditions would favor an SN2 reaction on 2-bromo-3-methylbutane?
A) weak nucleophile in a protic solvent
B) weak nucleophile in an aprotic solvent
C) strong nucleophile in a protic solvent
D) strong nucleophile in an aprotic solvent
A) weak nucleophile in a protic solvent
B) weak nucleophile in an aprotic solvent
C) strong nucleophile in a protic solvent
D) strong nucleophile in an aprotic solvent
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76
Which of the following is an aprotic solvent? 
A) I
B) II
C) III
D) IV
E) none of these

A) I
B) II
C) III
D) IV
E) none of these
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77
Identify the type of elimination in an E2 mechanism.
A) alpha elimination
B) beta elimination
C) gamma elimination
D) delta elimination
E) omega elimination
A) alpha elimination
B) beta elimination
C) gamma elimination
D) delta elimination
E) omega elimination
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78
Draw the structure of 2,3-dimethyl-1-pentene.
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79
Which of the following describes the difference between protic and aprotic solvents?
A) protic solvents stabilize anions only
B) aprotic solvents stabilize anions only
C) protic solvents stabilize cations only
D) aprotic solvents stabilize both cations and anions
E) protic solvents stabilize both cations and anions
A) protic solvents stabilize anions only
B) aprotic solvents stabilize anions only
C) protic solvents stabilize cations only
D) aprotic solvents stabilize both cations and anions
E) protic solvents stabilize both cations and anions
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80
Provide a curved arrow mechanism for the following SN2 reaction. 

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