Deck 9: Nucleophilic Substitution and Beta-Elimination

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Question
The reaction of tert-butyl bromide, (CH3)3CBr, with methanol in an inert solvent proceeds by an SN1 mechanism to give tert-butyl methyl ether, (CH3)3COCH3. What is the effect of doubling the concentration of methanol on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
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Question
What is the equation for the rate of formation of 2-methoxypropane, CH3CH(OCH3)CH3, from the reaction of 2-bromopropane (i-PrBr) with methanol?

A)Rate = k [i-PrBr]
B)Rate = k [i-PrBr]2
C)Rate = k [CH3OH]
D)Rate = k [i-PrBr][CH3OH]
Question
Which of the following reactions corresponds to a substitution?

A)propene \rarr 1,2-dibromopropane
B)1-iodopropane \rarr propene
C)propene \rarr propane
D)1-iodopropane \rarr 1-bromopropane
Question
What is the equation for the rate of formation of tert-butyl alcohol from the reaction of tert-butyl bromide (t-BuBr) with water by an SN1 mechanism?

A)Rate = k [t-BuBr]
B)Rate = k [t-BuBr][H2O]
C)Rate = k [H2O]
D)Rate = k [t-BuBr]2
Question
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium azide, NaN3?

A)1-fluorohexane
B)1-chlorohexane
C)1-bromohexane
D)1-iodohexane
Question
Which of the following alkyl halides undergoes the fastest solvolysis reaction with formic acid, HCOOH?

A)tert-butyl fluoride
B)tert-butyl chloride
C)tert-butyl bromide
D)tert-butyl iodide
Question
Which of the following statements related to SN1 reactions is not true?

A)The SN1 reaction can be described as a heterolytic bond cleavage followed by nucleophilic attack
B)Carbocations are electrophilic
C)The charged carbon atom of a carbocation has an unfilled valence shell
D)Nucleophiles are Lewis acids
Question
Which of the following reactions corresponds to a substitution?

A)tert-butanol \rarr tert-butyl chloride
B)tert-butanol \rarr 2-methylpropene
C)3,3-dimethyl-2-butanol \rarr 2,3-dimethyl-2-butene
D)cyclohexene \rarr 1,2-dichlorocyclohexane
Question
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium methylthiolate, NaSMe?

A)methyl iodide
B)ethyl iodide
C)2-bromopropane
D)tert-butyl chloride
Question
The reaction of methyl iodide with sodium azide, NaN3, proceeds by an SN2 mechanism. What is the effect of doubling the concentration of NaN3 on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
Question
Which of the following alkyl halides undergoes the fastest solvolysis reaction with methanol, CH3OH?

A)methyl chloride
B)ethyl chloride
C)2-chloropropane
D)tert-butyl chloride
Question
What is the equation for the rate of formation of 1-iodobutane from the reaction of 1-chlorobutane (BuCl) with NaI by an SN2 mechanism?

A)Rate = k [BuCl]
B)Rate = k [BuCl][NaI]
C)Rate = k [NaI]
D)Rate = k [BuCl]2
Question
Which of the following is the best set of conditions for the preparation of tert-butyl methyl ether?

A)tert-butyl fluoride and NaOCH3 in CH3OH
B)methanol and sodium tert-butoxide in tert-butanol
C)fluoromethane and sodium tert-butoxide in tert-butanol
D)tert-butyl bromide and CH3OH
Question
Which of the following is best set of conditions for the preparation of tert-butanol?

A)tert-butyl fluoride in water
B)tert-butyl bromide in water
C)tert-butyl fluoride and NaOH in DMSO
D)tert-butyl bromide and NaOH in DMSO
Question
Which of the following alkyl halides undergoes the fastest solvolysis reaction with ethanol, CH3CH2OH?

A)methyl fluoride
B)ethyl bromide
C)2-chloropropane
D)tert-butyl bromide
Question
The reaction of tert-butyl chloride, (CH3)3CCl, with water in an inert solvent gives tert-butyl alcohol, (CH3)3COH. What is the effect of doubling the concentration of water on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
Question
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium cyanide, NaCN?

A)methyl iodide
B)ethyl iodide
C)2-iodopropane
D)tert-butyl iodide
Question
The reaction of 1-bromopropane with sodium iodide gives 1-iodopropane. What is the effect of doubling the concentration of NaI on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
Question
Which of the following statements related to SN1 reactions is not true?

A)The heterolysis of a bond between atoms which do not bear formal charges always produces a cation and an anion
B)The charged carbon atom of a carbocation has a complete octet of valence shell electrons
C)Carbocations are Lewis acids
D)Nucleophiles seek centers of low electron density
Question
What is the equation for the rate of formation of 2-methoxypropane, (CH3CH(OCH3)CH3, from the reaction of 2-bromopropane (i-PrBr) with sodium methoxide (NaOCH3)?

A)Rate = k [i-PrBr]
B)Rate = k [i-PrBr]2
C)Rate = k [NaOCH3]
D)Rate = k [i-PrBr][NaOCH3]
Question
What is the major product formed upon treatment of (R) 1-bromo-4-methylhexane with sodium cyanide?

A)(R) 1-cyano-4-methylhexane
B)(S) 1-cyano-4-methylhexane
C)(R) 4-methyl-1-hexene
D)(S) 4-methyl-1-hexene
Question
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 1 and 2 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 1 and 2
D)1, 2 and 3
Question
Which of the following solvents is the best choice for the reaction of 1-chlorohexane with sodium bromide?

A)water
B)N,N-dimethylformamide
C)hexane
D)toluene, PhCH3
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 3 D)a mixture of 1 and 2 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 3
D)a mixture of 1 and 2
Question
What is the major organic product(s) obtained from the following reaction? <strong>What is the major organic product(s) obtained from the following reaction?  </strong> A)3-methyl-1-pentyne B)3-methyl-2-pentyne C)1-propene + propyne D)4-methyl-2-pentene <div style=padding-top: 35px>

A)3-methyl-1-pentyne
B)3-methyl-2-pentyne
C)1-propene + propyne
D)4-methyl-2-pentene
Question
Which of the following anions is the most nucleophilic in polar protic solvents?

A)F-
B)Cl-
C)Br-
D)I-
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the major product formed upon treatment of (R) 2-bromohexane with sodium cyanide?

A)(R) 2-cyanohexane
B)(S) 2-cyanohexane
C)1-hexene
D)2-hexene
Question
Which of the following anions is the most nucleophilic in polar aprotic solvents?

A)F-
B)Cl-
C)Br-
D)I-
Question
In which of the following solvents would the reaction of 1-bromobutane with sodium azide, NaN3, proceed the fastest?

A)acetic acid
B)ethanol
C)water
D)acetonitrile
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 3 D)a mixture of 1 and 2 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 3
D)a mixture of 1 and 2
Question
What is the major organic product(s) obtained from the following reaction? <strong>What is the major organic product(s) obtained from the following reaction?  </strong> A)1-hexyne B)2-hexyne C)propene + propyne D)propane + propyne <div style=padding-top: 35px>

A)1-hexyne
B)2-hexyne
C)propene + propyne
D)propane + propyne
Question
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 1 and 2 D)1, 2 and 3 <div style=padding-top: 35px>

A)only 1
B)only 2
C)only 1 and 2
D)1, 2 and 3
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following is the most nucleophilic?

A)sodium ethoxide
B)acetic acid
C)methanol
D)water
Question
Which of the following compounds is the most nucleophilic in polar protic solvents?

A)H2O
B)NH3
C)H2S
D)PH3
Question
Which of the following solvents is the best choice for the reaction of 1-chlorohexane with sodium bromide?

A)dimethylsulfoxide
B)water
C)hexane
D)toluene, PhCH3
Question
Which of the following is not a characteristic of SN1 reactions?

A)the electrophilic carbon undergoes inversion of stereochemistry
B)the rate is proportional to the concentration of substrate
C)the reaction proceeds faster in a more polar solvent
D)the rate is independent of the concentration of nucleophile
Question
Which of the following alkyl bromides reacts the slowest with NaSCH3 in DMF? <strong>Which of the following alkyl bromides reacts the slowest with NaSCH<sub>3</sub> in DMF?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following represents the transition state of the rate-determining step in the SN1 reaction between tert-butyl chloride and water? <strong>Which of the following represents the transition state of the rate-determining step in the S<sub>N</sub>1 reaction between tert-butyl chloride and water?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following statements is true regarding the reactivity of 1 and 2 with potassium tert-butoxide? <strong>Which of the following statements is true regarding the reactivity of 1 and 2 with potassium tert-butoxide?  </strong> A)1 reacts faster than 2 B)1 and 2 give different dehydrochlorinated products C)2 reacts by elimination whereas 1 reacts by substitution D)1 reacts by elimination whereas 2 reacts by substitution <div style=padding-top: 35px>

A)1 reacts faster than 2
B)1 and 2 give different dehydrochlorinated products
C)2 reacts by elimination whereas 1 reacts by substitution
D)1 reacts by elimination whereas 2 reacts by substitution
Question
Which of the following energy diagrams represents the course of an exothermic E1 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic E1 reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the major elimination product obtained from the following reaction? <strong>What is the major elimination product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the role of tetrabutylammonium chloride as a phase transfer catalyst in the reaction of 1-chlorooctane and sodium cyanide in a mixture of water and CH2Cl2?

A)it transfers 1-chlorooctane into the aqueous phase
B)it transfers cyanide anion into the organic phase
C)it makes water and dichloromethane miscible
D)it transfers the sodium cation into the organic phase
Question
Which of the following is most likely to undergo rearrangement during reaction with methanol? <strong>Which of the following is most likely to undergo rearrangement during reaction with methanol?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following anions is the best leaving group in an SN1 reaction?

A)F-
B)HO-
C)NH2-
D)Cl-
Question
Which of the following is the best leaving group in an SN2 reaction?

A)F-
B)H3C-
C)CH3O2SO-
D)HO-
Question
Which of the following energy diagrams represents the course of an exothermic SN1 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic S<sub>N</sub>1 reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following energy diagrams represents the course of an exothermic E2 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic E2 reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following statements is true regarding the reaction of tert-butyl bromide with water?

A)the rate is proportional to the concentration of tert-butyl bromide
B)the rate is proportional to the concentration of water
C)the rate is independent of the identity of the solvent
D)the rate of the reaction is independent of the temperature
Question
Which of the following is not a characteristic of SN2 reactions?

A)the electrophilic carbon undergoes inversion of stereochemistry
B)the rate is proportional to the concentration of substrate
C)the rate is proportional to the concentration of nucleophile
D)the rate is independent of the solvent
Question
Which of the following compounds undergoes the most rapid hydrolysis reaction? <strong>Which of the following compounds undergoes the most rapid hydrolysis reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following statements is not true regarding SN2 reactions?

A)A carbocation intermediate is formed.
B)The mechanism has only one step.
C)Aprotic solvents are good choices for SN1 reactions.
D)The stereochemical outcome is inversion at the carbon bearing the leaving group.
Question
Which of the following statements is not true regarding SN1 reactions?

A)A carbocation intermediate is formed.
B)The mechanism has only one step.
C)Polar, protic solvents are good choices for SN1 reactions.
D)The stereochemical outcome is racemization at the carbon bearing the leaving group.
Question
Which of the following statements is not true regarding the SN2 reaction of (R)-2-bromobutane with sodium cyanide?

A)the reaction proceeds with inversion of configuration
B)the rate is proportional to the concentration of sodium cyanide
C)the rate is proportional to the concentration of (R)-2-bromobutane
D)the rate of the reaction is independent of the identity of the solvent
Question
Which of the following energy diagrams represents the course of an exothermic SN2 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic S<sub>N</sub>2 reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl iodide and water leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl iodide and water leading to elimination?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following sets consists of only polar aprotic solvents?

A)water, hexane, methanol
B)acetic acid, DMF, toluene
C)DMSO, ethanol, acetonitrile
D)DMF, acetonitrile, DMSO
Question
What is the best choice of reagent to perform the following transformation? <strong>What is the best choice of reagent to perform the following transformation?  </strong> A)H<sub>2</sub>SO<sub>4</sub> B)H<sub>2</sub>O C)NaOCH<sub>3</sub> D)KOtBu <div style=padding-top: 35px>

A)H2SO4
B)H2O
C)NaOCH3
D)KOtBu
Question
Which of the following sets consists of only polar protic solvents?

A)water, DMF, DMSO
B)acetic acid, methanol, water
C)DMSO, ethanol, acetonitrile
D)DMF, acetonitrile, DMSO
Question
The rate law for the following reaction would be of the form Rate = k[A][B]. The rate law for the following reaction would be of the form Rate = k[A][B].  <div style=padding-top: 35px>
Question
The following energy diagram could represent an SN2 reaction. The following energy diagram could represent an S<sub>N</sub>2 reaction.  <div style=padding-top: 35px>
Question
The following reaction would be classified as an elimination. The following reaction would be classified as an elimination.  <div style=padding-top: 35px>
Question
Which of the following most favors elimination rather substitution in a reaction with sodium methoxide?

A)bromomethane
B)bromoethane
C)1-bromopropane
D)2-bromopropane
Question
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
The following reaction would have a faster rate in a higher polarity solvent than one of low polarity. The following reaction would have a faster rate in a higher polarity solvent than one of low polarity.  <div style=padding-top: 35px>
Question
In the following reaction the cyanide ion is both a nucleophile and a Lewis acid. In the following reaction the cyanide ion is both a nucleophile and a Lewis acid.  <div style=padding-top: 35px>
Question
HCl is the electrophile in the following reaction. HCl is the electrophile in the following reaction.  <div style=padding-top: 35px>
Question
Which of the following represents the transition state of the reaction between methyl iodide and ammonia? <strong>Which of the following represents the transition state of the reaction between methyl iodide and ammonia?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
The first step in the mechanism for the following reaction would be the formation of a secondary carbocation. The first step in the mechanism for the following reaction would be the formation of a secondary carbocation.  <div style=padding-top: 35px>
Question
Which of the following represents the transition state of the rate-determining step in the reaction between 2-chloropropane and sodium amide leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between 2-chloropropane and sodium amide leading to elimination?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol leading to elimination?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
What is the best choice of reagent to perform the following transformation? <strong>What is the best choice of reagent to perform the following transformation?  </strong> A)H<sub>2</sub>SO<sub>4</sub> B)H<sub>2</sub>O C)NaOCH<sub>3</sub> D)KOtBu <div style=padding-top: 35px>

A)H2SO4
B)H2O
C)NaOCH3
D)KOtBu
Question
Which of the following most favors elimination rather substitution in a reaction with 2-bromopropane?

A)sodium methoxide
B)sodium ethoxide
C)sodium isoproxide
D)sodium tert-butoxide
Question
Which of the following represents the transition state of the rate-determining step in the reaction between 2-bromopropane and sodium methoxide leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between 2-bromopropane and sodium methoxide leading to elimination?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
Question
Which of the following represents the transition state of the reaction between methyl bromide and sodium methylthiolate, NaSCH3? <strong>Which of the following represents the transition state of the reaction between methyl bromide and sodium methylthiolate, NaSCH<sub>3</sub>?  </strong> A)1 B)2 C)3 D)4 <div style=padding-top: 35px>

A)1
B)2
C)3
D)4
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Deck 9: Nucleophilic Substitution and Beta-Elimination
1
The reaction of tert-butyl bromide, (CH3)3CBr, with methanol in an inert solvent proceeds by an SN1 mechanism to give tert-butyl methyl ether, (CH3)3COCH3. What is the effect of doubling the concentration of methanol on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
the rate remains the same
2
What is the equation for the rate of formation of 2-methoxypropane, CH3CH(OCH3)CH3, from the reaction of 2-bromopropane (i-PrBr) with methanol?

A)Rate = k [i-PrBr]
B)Rate = k [i-PrBr]2
C)Rate = k [CH3OH]
D)Rate = k [i-PrBr][CH3OH]
Rate = k [i-PrBr]
3
Which of the following reactions corresponds to a substitution?

A)propene \rarr 1,2-dibromopropane
B)1-iodopropane \rarr propene
C)propene \rarr propane
D)1-iodopropane \rarr 1-bromopropane
1-iodopropane \rarr 1-bromopropane
4
What is the equation for the rate of formation of tert-butyl alcohol from the reaction of tert-butyl bromide (t-BuBr) with water by an SN1 mechanism?

A)Rate = k [t-BuBr]
B)Rate = k [t-BuBr][H2O]
C)Rate = k [H2O]
D)Rate = k [t-BuBr]2
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5
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium azide, NaN3?

A)1-fluorohexane
B)1-chlorohexane
C)1-bromohexane
D)1-iodohexane
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6
Which of the following alkyl halides undergoes the fastest solvolysis reaction with formic acid, HCOOH?

A)tert-butyl fluoride
B)tert-butyl chloride
C)tert-butyl bromide
D)tert-butyl iodide
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7
Which of the following statements related to SN1 reactions is not true?

A)The SN1 reaction can be described as a heterolytic bond cleavage followed by nucleophilic attack
B)Carbocations are electrophilic
C)The charged carbon atom of a carbocation has an unfilled valence shell
D)Nucleophiles are Lewis acids
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8
Which of the following reactions corresponds to a substitution?

A)tert-butanol \rarr tert-butyl chloride
B)tert-butanol \rarr 2-methylpropene
C)3,3-dimethyl-2-butanol \rarr 2,3-dimethyl-2-butene
D)cyclohexene \rarr 1,2-dichlorocyclohexane
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9
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium methylthiolate, NaSMe?

A)methyl iodide
B)ethyl iodide
C)2-bromopropane
D)tert-butyl chloride
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10
The reaction of methyl iodide with sodium azide, NaN3, proceeds by an SN2 mechanism. What is the effect of doubling the concentration of NaN3 on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
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11
Which of the following alkyl halides undergoes the fastest solvolysis reaction with methanol, CH3OH?

A)methyl chloride
B)ethyl chloride
C)2-chloropropane
D)tert-butyl chloride
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12
What is the equation for the rate of formation of 1-iodobutane from the reaction of 1-chlorobutane (BuCl) with NaI by an SN2 mechanism?

A)Rate = k [BuCl]
B)Rate = k [BuCl][NaI]
C)Rate = k [NaI]
D)Rate = k [BuCl]2
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13
Which of the following is the best set of conditions for the preparation of tert-butyl methyl ether?

A)tert-butyl fluoride and NaOCH3 in CH3OH
B)methanol and sodium tert-butoxide in tert-butanol
C)fluoromethane and sodium tert-butoxide in tert-butanol
D)tert-butyl bromide and CH3OH
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14
Which of the following is best set of conditions for the preparation of tert-butanol?

A)tert-butyl fluoride in water
B)tert-butyl bromide in water
C)tert-butyl fluoride and NaOH in DMSO
D)tert-butyl bromide and NaOH in DMSO
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15
Which of the following alkyl halides undergoes the fastest solvolysis reaction with ethanol, CH3CH2OH?

A)methyl fluoride
B)ethyl bromide
C)2-chloropropane
D)tert-butyl bromide
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16
The reaction of tert-butyl chloride, (CH3)3CCl, with water in an inert solvent gives tert-butyl alcohol, (CH3)3COH. What is the effect of doubling the concentration of water on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
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17
Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium cyanide, NaCN?

A)methyl iodide
B)ethyl iodide
C)2-iodopropane
D)tert-butyl iodide
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18
The reaction of 1-bromopropane with sodium iodide gives 1-iodopropane. What is the effect of doubling the concentration of NaI on the rate of the reaction?

A)the rate remains the same
B)the rate decreases by a factor of 2
C)the rate increases by a factor of 2
D)the rate increases by a factor of 4
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19
Which of the following statements related to SN1 reactions is not true?

A)The heterolysis of a bond between atoms which do not bear formal charges always produces a cation and an anion
B)The charged carbon atom of a carbocation has a complete octet of valence shell electrons
C)Carbocations are Lewis acids
D)Nucleophiles seek centers of low electron density
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20
What is the equation for the rate of formation of 2-methoxypropane, (CH3CH(OCH3)CH3, from the reaction of 2-bromopropane (i-PrBr) with sodium methoxide (NaOCH3)?

A)Rate = k [i-PrBr]
B)Rate = k [i-PrBr]2
C)Rate = k [NaOCH3]
D)Rate = k [i-PrBr][NaOCH3]
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21
What is the major product formed upon treatment of (R) 1-bromo-4-methylhexane with sodium cyanide?

A)(R) 1-cyano-4-methylhexane
B)(S) 1-cyano-4-methylhexane
C)(R) 4-methyl-1-hexene
D)(S) 4-methyl-1-hexene
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22
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 1 and 2 D)1, 2 and 3

A)only 1
B)only 2
C)only 1 and 2
D)1, 2 and 3
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23
Which of the following solvents is the best choice for the reaction of 1-chlorohexane with sodium bromide?

A)water
B)N,N-dimethylformamide
C)hexane
D)toluene, PhCH3
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24
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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25
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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26
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 3 D)a mixture of 1 and 2

A)only 1
B)only 2
C)only 3
D)a mixture of 1 and 2
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27
What is the major organic product(s) obtained from the following reaction? <strong>What is the major organic product(s) obtained from the following reaction?  </strong> A)3-methyl-1-pentyne B)3-methyl-2-pentyne C)1-propene + propyne D)4-methyl-2-pentene

A)3-methyl-1-pentyne
B)3-methyl-2-pentyne
C)1-propene + propyne
D)4-methyl-2-pentene
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28
Which of the following anions is the most nucleophilic in polar protic solvents?

A)F-
B)Cl-
C)Br-
D)I-
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29
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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30
What is the major product formed upon treatment of (R) 2-bromohexane with sodium cyanide?

A)(R) 2-cyanohexane
B)(S) 2-cyanohexane
C)1-hexene
D)2-hexene
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31
Which of the following anions is the most nucleophilic in polar aprotic solvents?

A)F-
B)Cl-
C)Br-
D)I-
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32
In which of the following solvents would the reaction of 1-bromobutane with sodium azide, NaN3, proceed the fastest?

A)acetic acid
B)ethanol
C)water
D)acetonitrile
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33
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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34
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 3 D)a mixture of 1 and 2

A)only 1
B)only 2
C)only 3
D)a mixture of 1 and 2
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35
What is the major organic product(s) obtained from the following reaction? <strong>What is the major organic product(s) obtained from the following reaction?  </strong> A)1-hexyne B)2-hexyne C)propene + propyne D)propane + propyne

A)1-hexyne
B)2-hexyne
C)propene + propyne
D)propane + propyne
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36
What is(are) the major organic product(s) obtained from the following substitution reaction? <strong>What is(are) the major organic product(s) obtained from the following substitution reaction?  </strong> A)only 1 B)only 2 C)only 1 and 2 D)1, 2 and 3

A)only 1
B)only 2
C)only 1 and 2
D)1, 2 and 3
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37
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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38
Which of the following is the most nucleophilic?

A)sodium ethoxide
B)acetic acid
C)methanol
D)water
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39
Which of the following compounds is the most nucleophilic in polar protic solvents?

A)H2O
B)NH3
C)H2S
D)PH3
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40
Which of the following solvents is the best choice for the reaction of 1-chlorohexane with sodium bromide?

A)dimethylsulfoxide
B)water
C)hexane
D)toluene, PhCH3
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41
Which of the following is not a characteristic of SN1 reactions?

A)the electrophilic carbon undergoes inversion of stereochemistry
B)the rate is proportional to the concentration of substrate
C)the reaction proceeds faster in a more polar solvent
D)the rate is independent of the concentration of nucleophile
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42
Which of the following alkyl bromides reacts the slowest with NaSCH3 in DMF? <strong>Which of the following alkyl bromides reacts the slowest with NaSCH<sub>3</sub> in DMF?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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43
Which of the following represents the transition state of the rate-determining step in the SN1 reaction between tert-butyl chloride and water? <strong>Which of the following represents the transition state of the rate-determining step in the S<sub>N</sub>1 reaction between tert-butyl chloride and water?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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44
Which of the following statements is true regarding the reactivity of 1 and 2 with potassium tert-butoxide? <strong>Which of the following statements is true regarding the reactivity of 1 and 2 with potassium tert-butoxide?  </strong> A)1 reacts faster than 2 B)1 and 2 give different dehydrochlorinated products C)2 reacts by elimination whereas 1 reacts by substitution D)1 reacts by elimination whereas 2 reacts by substitution

A)1 reacts faster than 2
B)1 and 2 give different dehydrochlorinated products
C)2 reacts by elimination whereas 1 reacts by substitution
D)1 reacts by elimination whereas 2 reacts by substitution
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45
Which of the following energy diagrams represents the course of an exothermic E1 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic E1 reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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46
What is the major elimination product obtained from the following reaction? <strong>What is the major elimination product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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47
What is the role of tetrabutylammonium chloride as a phase transfer catalyst in the reaction of 1-chlorooctane and sodium cyanide in a mixture of water and CH2Cl2?

A)it transfers 1-chlorooctane into the aqueous phase
B)it transfers cyanide anion into the organic phase
C)it makes water and dichloromethane miscible
D)it transfers the sodium cation into the organic phase
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48
Which of the following is most likely to undergo rearrangement during reaction with methanol? <strong>Which of the following is most likely to undergo rearrangement during reaction with methanol?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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49
Which of the following anions is the best leaving group in an SN1 reaction?

A)F-
B)HO-
C)NH2-
D)Cl-
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50
Which of the following is the best leaving group in an SN2 reaction?

A)F-
B)H3C-
C)CH3O2SO-
D)HO-
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51
Which of the following energy diagrams represents the course of an exothermic SN1 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic S<sub>N</sub>1 reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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52
Which of the following energy diagrams represents the course of an exothermic E2 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic E2 reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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53
Which of the following statements is true regarding the reaction of tert-butyl bromide with water?

A)the rate is proportional to the concentration of tert-butyl bromide
B)the rate is proportional to the concentration of water
C)the rate is independent of the identity of the solvent
D)the rate of the reaction is independent of the temperature
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54
Which of the following is not a characteristic of SN2 reactions?

A)the electrophilic carbon undergoes inversion of stereochemistry
B)the rate is proportional to the concentration of substrate
C)the rate is proportional to the concentration of nucleophile
D)the rate is independent of the solvent
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55
Which of the following compounds undergoes the most rapid hydrolysis reaction? <strong>Which of the following compounds undergoes the most rapid hydrolysis reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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56
Which of the following statements is not true regarding SN2 reactions?

A)A carbocation intermediate is formed.
B)The mechanism has only one step.
C)Aprotic solvents are good choices for SN1 reactions.
D)The stereochemical outcome is inversion at the carbon bearing the leaving group.
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57
Which of the following statements is not true regarding SN1 reactions?

A)A carbocation intermediate is formed.
B)The mechanism has only one step.
C)Polar, protic solvents are good choices for SN1 reactions.
D)The stereochemical outcome is racemization at the carbon bearing the leaving group.
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58
Which of the following statements is not true regarding the SN2 reaction of (R)-2-bromobutane with sodium cyanide?

A)the reaction proceeds with inversion of configuration
B)the rate is proportional to the concentration of sodium cyanide
C)the rate is proportional to the concentration of (R)-2-bromobutane
D)the rate of the reaction is independent of the identity of the solvent
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59
Which of the following energy diagrams represents the course of an exothermic SN2 reaction? <strong>Which of the following energy diagrams represents the course of an exothermic S<sub>N</sub>2 reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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60
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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61
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl iodide and water leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl iodide and water leading to elimination?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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62
Which of the following sets consists of only polar aprotic solvents?

A)water, hexane, methanol
B)acetic acid, DMF, toluene
C)DMSO, ethanol, acetonitrile
D)DMF, acetonitrile, DMSO
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63
What is the best choice of reagent to perform the following transformation? <strong>What is the best choice of reagent to perform the following transformation?  </strong> A)H<sub>2</sub>SO<sub>4</sub> B)H<sub>2</sub>O C)NaOCH<sub>3</sub> D)KOtBu

A)H2SO4
B)H2O
C)NaOCH3
D)KOtBu
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64
Which of the following sets consists of only polar protic solvents?

A)water, DMF, DMSO
B)acetic acid, methanol, water
C)DMSO, ethanol, acetonitrile
D)DMF, acetonitrile, DMSO
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65
The rate law for the following reaction would be of the form Rate = k[A][B]. The rate law for the following reaction would be of the form Rate = k[A][B].
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66
The following energy diagram could represent an SN2 reaction. The following energy diagram could represent an S<sub>N</sub>2 reaction.
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67
The following reaction would be classified as an elimination. The following reaction would be classified as an elimination.
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68
Which of the following most favors elimination rather substitution in a reaction with sodium methoxide?

A)bromomethane
B)bromoethane
C)1-bromopropane
D)2-bromopropane
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69
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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70
The following reaction would have a faster rate in a higher polarity solvent than one of low polarity. The following reaction would have a faster rate in a higher polarity solvent than one of low polarity.
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71
In the following reaction the cyanide ion is both a nucleophile and a Lewis acid. In the following reaction the cyanide ion is both a nucleophile and a Lewis acid.
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72
HCl is the electrophile in the following reaction. HCl is the electrophile in the following reaction.
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73
Which of the following represents the transition state of the reaction between methyl iodide and ammonia? <strong>Which of the following represents the transition state of the reaction between methyl iodide and ammonia?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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74
The first step in the mechanism for the following reaction would be the formation of a secondary carbocation. The first step in the mechanism for the following reaction would be the formation of a secondary carbocation.
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75
Which of the following represents the transition state of the rate-determining step in the reaction between 2-chloropropane and sodium amide leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between 2-chloropropane and sodium amide leading to elimination?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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76
Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between tert-butyl bromide and methanol leading to elimination?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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77
What is the best choice of reagent to perform the following transformation? <strong>What is the best choice of reagent to perform the following transformation?  </strong> A)H<sub>2</sub>SO<sub>4</sub> B)H<sub>2</sub>O C)NaOCH<sub>3</sub> D)KOtBu

A)H2SO4
B)H2O
C)NaOCH3
D)KOtBu
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78
Which of the following most favors elimination rather substitution in a reaction with 2-bromopropane?

A)sodium methoxide
B)sodium ethoxide
C)sodium isoproxide
D)sodium tert-butoxide
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79
Which of the following represents the transition state of the rate-determining step in the reaction between 2-bromopropane and sodium methoxide leading to elimination? <strong>Which of the following represents the transition state of the rate-determining step in the reaction between 2-bromopropane and sodium methoxide leading to elimination?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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80
Which of the following represents the transition state of the reaction between methyl bromide and sodium methylthiolate, NaSCH3? <strong>Which of the following represents the transition state of the reaction between methyl bromide and sodium methylthiolate, NaSCH<sub>3</sub>?  </strong> A)1 B)2 C)3 D)4

A)1
B)2
C)3
D)4
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