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


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

E) A) and B)
F) All of the above

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What is the classification for the following halide? 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

E) B) and C)
F) A) and D)

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Which of the following compounds will undergo the fastest SN1 reaction? Explain your choice. Which of the following compounds will undergo the fastest S<sub>N</sub>1 reaction? Explain your choice.

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Compound IV The carb...

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What substitution reaction mechanism is most likely for the following compound? What substitution reaction mechanism is most likely for the following compound?   A)  S<sub>N</sub>1 B)  S<sub>N</sub>2 C)  Either S<sub>N</sub>1 or S<sub>N</sub>2 D)  None of these


A) SN1
B) SN2
C) Either SN1 or SN2
D) None of these

E) B) and C)
F) None of the above

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Provide the structure for (4R,8S)-4-iodo-2,2,8-trimethyldecane.

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Predict the product for the following reaction. 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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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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Consider the following SN2 reaction, 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? 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

F) A) and D)
G) B) and E)

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What is the IUPAC name for the following compound? 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

E) A) and D)
F) All of the above

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Which of the following is a tertiary alkyl halide?


A) (CH3) 2CHCH2Cl
B) (CH3) 2CClCH2CH3
C) (CH3) 2CHCHClCH3
D) (CH3) 2CHCH2CHClCH2CH3

E) A) and B)
F) B) and D)

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


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

E) All of the above
F) B) and C)

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


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

E) A) and B)
F) All of the above

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Which of the following is the rate equation for the following SN2 reaction? Which of the following is the rate equation for the following S<sub>N</sub>2 reaction?   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

F) A) and B)
G) A) and C)

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What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?

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(1R, 3S)-3...

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What substitution reaction mechanism is most likely for the following compound? What substitution reaction mechanism is most likely for the following compound?   A)  S<sub>N</sub>1 B)  S<sub>N</sub>2 C)  Either S<sub>N</sub>1 or S<sub>N</sub>2 D)  None of these


A) SN1
B) SN2
C) Either SN1 or SN2
D) None of these

E) All of the above
F) A) and C)

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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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Which of the following is a mechanism for an SN2 reaction? Which of the following is a mechanism for an S<sub>N</sub>2 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

F) A) and C)
G) C) and E)

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Which of the following is not a possible step in a substitution reaction? Which of the following is not a possible step in a substitution reaction?   A)  I B)  II C)  III D)  IV


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

E) B) and C)
F) A) and D)

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What substitution reaction mechanism is most likely for the following conversion? What substitution reaction mechanism is most likely for the following conversion?   A)  S<sub>N</sub>1 B)  S<sub>N</sub>2 C)  Either S<sub>N</sub>1 or S<sub>N</sub>2 D)  None of these


A) SN1
B) SN2
C) Either SN1 or SN2
D) None of these

E) A) and B)
F) C) and D)

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What is the IUPAC name for the following compound? 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

F) A) and B)
G) A) and C)

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