Deck 7: Alkyl Halides: Nucleophilic Substitution and Elimination Reactions

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Question
Which of the following is a primary alkyl halide?

A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
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Question
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> 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 <div style=padding-top: 35px>

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
Question
For the following reaction, label the nucleophile, electrophile, and leaving group. For the following reaction, label the nucleophile, electrophile, and leaving group.  <div style=padding-top: 35px>
Question
What is the nucleophile in the following reaction? <strong>What is the nucleophile in the following reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
What is the nucleophile in the following reaction? <strong>What is the nucleophile in the following reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following is a substitution reaction? <strong>Which of the following is a substitution reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following is an elimination reaction? <strong>Which of the following is an elimination reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following is an elimination reaction? <strong>Which of the following is an elimination reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
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
Question
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
Question
What is the electrophile in the following reaction? <strong>What is the electrophile in the following reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
What is the electrophile in the following reaction? <strong>What is the electrophile in the following reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following is a tertiary alkyl halide?

A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CHClCH2CH3
Question
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> A) Chlorocyclopentane B) 2-Chloro-1-methylcyclopentane C) 1-Methyl-2-chlorocyclopentane D) 1-Chloro-2-methylcyclopentane <div style=padding-top: 35px>

A) Chlorocyclopentane
B) 2-Chloro-1-methylcyclopentane
C) 1-Methyl-2-chlorocyclopentane
D) 1-Chloro-2-methylcyclopentane
Question
Which of the following is a substitution reaction? <strong>Which of the following is a substitution reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> A) 3-Fluorobutane B) 2-Fluorobutane C) (S)-2-Fluorobutane D) (R)-2-Fluorobutane <div style=padding-top: 35px>

A) 3-Fluorobutane
B) 2-Fluorobutane
C) (S)-2-Fluorobutane
D) (R)-2-Fluorobutane
Question
For the following reaction, label the nucleophile, electrophile, and leaving group. For the following reaction, label the nucleophile, electrophile, and leaving group.  <div style=padding-top: 35px>
Question
Which of the following is a substitution reaction? <strong>Which of the following is a substitution reaction?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following is a secondary alkyl halide?

A) (CH3)2CHCH2Cl
B) (CH3)2CClCH2CH3
C) (CH3)2CHCHClCH3
D) (CH3)2CHCH2CCl(CH3)2
Question
What is the classification for the following halide? <strong>What is the classification for the following halide?  </strong> A) primary halide B) secondary halide C) tertiary halide D) quaternary halide <div style=padding-top: 35px>

A) primary halide
B) secondary halide
C) tertiary halide
D) quaternary halide
Question
Provide the structure for (4R,8S)-4-iodo-2,2,8-trimethyldecane.
Question
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
Question
What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?  <div style=padding-top: 35px>
Question
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of 2-bromopentane is doubled and the concentration of CH<sub>3</sub>CH<sub>2</sub>COONa is halved?</strong> 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 <div style=padding-top: 35px> 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
Question
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of both 1-chloro-3-methylbutane and NaN<sub>3 </sub>is doubled?</strong> 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 <div style=padding-top: 35px> 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
Question
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>] <div style=padding-top: 35px>

A) Rate = k[CH3CH2CH2CHBrCH3]
B) Rate = k[NaN3]
C) Rate = k[CH3CH2CH2CHBrCH3] [NaBr]
D) Rate = k[CH3CH2CH2CHBrCH3] [NaN3]
E) Rate = k[CH3CH2CH2CHBrCH3]2 [NaN3]
Question
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
Question
What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?  <div style=padding-top: 35px>
Question
What is the correct structure for 2-bromo-3-methylbutane? <strong>What is the correct structure for 2-bromo-3-methylbutane?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> 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 <div style=padding-top: 35px>

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
Question
What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?  <div style=padding-top: 35px>
Question
Provide the structure for 1-chloro-4-isopropylheptane.
Question
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
Question
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of NaN<sub>3 </sub>is tripled?</strong> 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 <div style=padding-top: 35px> 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
Question
What is the correct structure for (2S,5R)-2-fluoro-5-methylnonane? <strong>What is the correct structure for (2S,5R)-2-fluoro-5-methylnonane?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of 1-chloro-3-methylbutane is doubled?</strong> 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 <div style=padding-top: 35px> 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
Question
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> <div style=padding-top: 35px>

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
Question
Provide a curved arrow mechanism for the following SN2 reaction Provide a curved arrow mechanism for the following S<sub>N</sub>2 reaction  <div style=padding-top: 35px>
Question
What is the correct structure for 3-ethyl-1-iodocyclohexane? <strong>What is the correct structure for 3-ethyl-1-iodocyclohexane?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Provide the structure for cis-1,2-dibromocyclopentane.
Question
Predict the product for the following SN2 reaction. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px> <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) None of these
Question
Draw the transition state for the following SN2 reaction. <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <div style=padding-top: 35px> <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Which of the following alkyl halides will undergo the fastest SN2 reaction? <strong>Which of the following alkyl halides will undergo the fastest S<sub>N</sub>2 reaction?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Draw the transition state for the following SN2 reaction. <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <div style=padding-top: 35px> <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Predict the product for the following SN2 reaction. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Rank the following compounds from most to least reactive in an SN2 reaction. <strong>Rank the following compounds from most to least reactive in an S<sub>N</sub>2 reaction.  </strong> 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 <div style=padding-top: 35px>

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
Question
Which of the following is a mechanism for an SN2 reaction? <strong>Which of the following is a mechanism for an S<sub>N</sub>2 reaction?  </strong> A) I B) II C) III D) IV E) Both I & II <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) Both I & II
Question
Provide a curved arrow mechanism and predict the product for the following SN2 reaction. Provide a curved arrow mechanism and predict the product for the following S<sub>N</sub>2 reaction.  <div style=padding-top: 35px>
Question
Predict the product for the following reaction.
(1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN3
Predict the product for the following reaction. (1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN<sub>3</sub> <sub> </sub>  <div style=padding-top: 35px>
Question
Draw the transition state for the following reaction.
(S)-1-iodo-3-methylpentane + NaSCH3
Question
Predict the product for the following reaction. <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px> <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) None of these
Question
Which of the following alkyl halides will undergo the slowest SN2 reaction? <strong>Which of the following alkyl halides will undergo the slowest S<sub>N</sub>2 reaction?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Predict the product for the following reaction. <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Draw the potential energy diagram for the following SN2 reaction. <strong>Draw the potential energy diagram for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of the above <div style=padding-top: 35px> <strong>Draw the potential energy diagram for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of the above <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) None of the above
Question
Predict the product for the following reaction. Predict the product for the following reaction.  <div style=padding-top: 35px>
Question
Rank the following compounds from most to least reactive in an SN2 reaction. <strong>Rank the following compounds from most to least reactive in an S<sub>N</sub>2 reaction.  </strong> 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 <div style=padding-top: 35px>

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
Question
Which of the following alkyl halides is essentially unreactive in an SN2 reaction? <strong>Which of the following alkyl halides is essentially unreactive in an S<sub>N</sub>2 reaction?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Provide a curved arrow mechanism and predict the product for the following reaction. Provide a curved arrow mechanism and predict the product for the following reaction.  <div style=padding-top: 35px>
Question
Predict the product for the following SN2 reaction. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px> <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) None of these
Question
Predict the product for the following SN2 reaction. <strong>Predict the product for the following S<sub>N</sub>2 reaction.  </strong> A) I B) II C) III D) IV E) Both I & II <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) Both I & II
Question
Predict the product for the following SN2 reaction. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Identify the IUPAC name for the following compound. <strong>Identify the IUPAC name for the following compound.  </strong> A) 1-methyl-2-cyclohexene B) 2-methylcyclohexene C) 3-methylcyclohexene D) 1-methyl-5-cyclohexene <div style=padding-top: 35px>

A) 1-methyl-2-cyclohexene
B) 2-methylcyclohexene
C) 3-methylcyclohexene
D) 1-methyl-5-cyclohexene
Question
Identify the methylating agent used in biological systems.

A) methyl iodide
B) S-adenosylmethionine
C) methylalanine
D) methylproline
E) methyl bromide
Question
Which of the following is a protic solvent? <strong>Which of the following is a protic solvent?  </strong> A) I B) II C) III D) IV E) none of these <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) none of these
Question
Describe a strong nucleophile.

A) an anion
B) a cation
C) a radical
D) a neutral compound
Question
Which of the following is NOT a nucleophile?

A) OH-
B) NH3
C) CH3OH
D) NH4+
E) All of these
Question
Which of the following is a strong nucleophile?

A) OH-
B) H2O
C) CH3OH
D) NH4+
E) All of these
Question
Which of the following is a weak nucleophile?

A) OH-
B) H2O
C) CH3O-
D) NH4+
E) All of these
Question
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
Question
Provide an IUPAC name for the following compound. Provide an IUPAC name for the following compound.  <div style=padding-top: 35px>
Question
Which of the following is the IUPAC name for the following compound? <strong>Which of the following is the IUPAC name for the following compound?  </strong> 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 <div style=padding-top: 35px>

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
Question
Predict the product for the following SN2 reaction. Predict the product for the following S<sub>N</sub>2 reaction.  <div style=padding-top: 35px>
Question
Which of the following shows a mechanism of a concerted elimination? <strong>Which of the following shows a mechanism of a concerted elimination?  </strong> A) I B) II C) III D) IV <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
Question
Predict the SN2 product and provide a curved arrow mechanism for the formation of the product. Predict the S<sub>N</sub>2 product and provide a curved arrow mechanism for the formation of the product.  <div style=padding-top: 35px>
Question
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
Question
Which of the following is an aprotic solvent? <strong>Which of the following is an aprotic solvent?  </strong> A) I B) II C) III D) IV E) none of these <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) none of these
Question
Identify the type of elimination in an E2 mechanism.

A) alpha elimination
B) beta elimination
C) gamma elimination
D) delta elimination
E) omega elimination
Question
Draw the structure of 2,3-dimethyl-1-pentene.
Question
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
Question
Provide a curved arrow mechanism for the following SN2 reaction. Provide a curved arrow mechanism for the following S<sub>N</sub>2 reaction.  <div style=padding-top: 35px>
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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
(CH3)2CHCH2Cl
2
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> 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. For the following reaction, label the nucleophile, electrophile, and leaving group.
4
What is the nucleophile in the following reaction? <strong>What is the nucleophile in the following reaction?  </strong> 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? <strong>What is the nucleophile in the following reaction?  </strong> 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? <strong>Which of the following is a substitution reaction?  </strong> 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? <strong>Which of the following is an elimination reaction?  </strong> 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? <strong>Which of the following is an elimination reaction?  </strong> 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
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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
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11
What is the electrophile in the following reaction? <strong>What is the electrophile in the following reaction?  </strong> 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? <strong>What is the electrophile in the following reaction?  </strong> 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
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14
What is the IUPAC name for the following compound? <strong>What is the IUPAC name for the following compound?  </strong> 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? <strong>Which of the following is a substitution reaction?  </strong> 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? <strong>What is the IUPAC name for the following compound?  </strong> 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. For the following reaction, label the nucleophile, electrophile, and leaving group.
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18
Which of the following is a substitution reaction? <strong>Which of the following is a substitution reaction?  </strong> 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
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20
What is the classification for the following halide? <strong>What is the classification for the following halide?  </strong> 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
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23
What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?
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24
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of 2-bromopentane is doubled and the concentration of CH<sub>3</sub>CH<sub>2</sub>COONa is halved?</strong> 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 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
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25
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of both 1-chloro-3-methylbutane and NaN<sub>3 </sub>is doubled?</strong> 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 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
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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>]

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
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28
What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?
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29
What is the correct structure for 2-bromo-3-methylbutane? <strong>What is the correct structure for 2-bromo-3-methylbutane?  </strong> 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? <strong>What is the IUPAC name for the following compound?  </strong> 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? 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
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34
Consider the following SN2 reaction, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of NaN<sub>3 </sub>is tripled?</strong> 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 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
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35
What is the correct structure for (2S,5R)-2-fluoro-5-methylnonane? <strong>What is the correct structure for (2S,5R)-2-fluoro-5-methylnonane?  </strong> 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, <strong>Consider the following S<sub>N</sub>2 reaction,   Assuming no other changes, what is the effect on the rate, if the concentration of 1-chloro-3-methylbutane is doubled?</strong> 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 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
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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>

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 Provide a curved arrow mechanism for the following S<sub>N</sub>2 reaction
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39
What is the correct structure for 3-ethyl-1-iodocyclohexane? <strong>What is the correct structure for 3-ethyl-1-iodocyclohexane?  </strong> 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. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> 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. <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> 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? <strong>Which of the following alkyl halides will undergo the fastest S<sub>N</sub>2 reaction?  </strong> 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. <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV <strong>Draw the transition state for the following S<sub>N</sub>2 reaction.    </strong> 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. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> 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. <strong>Rank the following compounds from most to least reactive in an S<sub>N</sub>2 reaction.  </strong> 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? <strong>Which of the following is a mechanism for an S<sub>N</sub>2 reaction?  </strong> 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. Provide a curved arrow mechanism and predict the product for the following S<sub>N</sub>2 reaction.
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49
Predict the product for the following reaction.
(1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN3
Predict the product for the following reaction. (1R, 3S)-1-bromo-3-sec-butylcyclopentane + NaN<sub>3</sub> <sub> </sub>
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50
Draw the transition state for the following reaction.
(S)-1-iodo-3-methylpentane + NaSCH3
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51
Predict the product for the following reaction. <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) None of these <strong>Predict the product for the following reaction.    </strong> 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? <strong>Which of the following alkyl halides will undergo the slowest S<sub>N</sub>2 reaction?  </strong> 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. <strong>Predict the product for the following reaction.    </strong> A) I B) II C) III D) IV E) V <strong>Predict the product for the following reaction.    </strong> 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. <strong>Draw the potential energy diagram for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of the above <strong>Draw the potential energy diagram for the following S<sub>N</sub>2 reaction.    </strong> 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. 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. <strong>Rank the following compounds from most to least reactive in an S<sub>N</sub>2 reaction.  </strong> 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? <strong>Which of the following alkyl halides is essentially unreactive in an S<sub>N</sub>2 reaction?  </strong> 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. 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. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) None of these <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> 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. <strong>Predict the product for the following S<sub>N</sub>2 reaction.  </strong> 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. <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> A) I B) II C) III D) IV E) V <strong>Predict the product for the following S<sub>N</sub>2 reaction.    </strong> 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. <strong>Identify the IUPAC name for the following compound.  </strong> 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
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64
Which of the following is a protic solvent? <strong>Which of the following is a protic solvent?  </strong> 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
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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
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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
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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
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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
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70
Provide an IUPAC name for the following compound. 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? <strong>Which of the following is the IUPAC name for the following compound?  </strong> 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. Predict the product for the following S<sub>N</sub>2 reaction.
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73
Which of the following shows a mechanism of a concerted elimination? <strong>Which of the following shows a mechanism of a concerted elimination?  </strong> 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. Predict the S<sub>N</sub>2 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
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76
Which of the following is an aprotic solvent? <strong>Which of the following is an aprotic solvent?  </strong> 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
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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
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80
Provide a curved arrow mechanism for the following SN2 reaction. Provide a curved arrow mechanism for the following S<sub>N</sub>2 reaction.
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