Deck 20: Amines

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Question
The correct structure of (S)-bicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (S)-bicyclo[2.2.1]heptan-2-amine is?  </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
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Question
The correct structure of bicyclo[1.1.0]butan-1-amine is? <strong>The correct structure of bicyclo[1.1.0]butan-1-amine is?  </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
The correct structure of (S)-N-methylbicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (S)-N-methylbicyclo[2.2.1]heptan-2-amine is?  </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
Which is a correct common name for the following substance? <strong>Which is a correct common name for the following substance?  </strong> A)Ethylethylisobutylamine B)Diethylisobutylamine C)sec-Butyldiethylamine D)Ethylethyl-sec-butylamine E)2-Diethylaminobutane <div style=padding-top: 35px>

A)Ethylethylisobutylamine
B)Diethylisobutylamine
C)sec-Butyldiethylamine
D)Ethylethyl-sec-butylamine
E)2-Diethylaminobutane
Question
What type of amine is piperidine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
What type of amine is quinoline?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
What type of amine is pyrrole?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
The correct structure of bicyclo[1.1.0]butan-2-amine is? <strong>The correct structure of bicyclo[1.1.0]butan-2-amine is?  </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
Which is a correct IUPAC name for the following substance? <strong>Which is a correct IUPAC name for the following substance?  </strong> A)N-Cyclopentyl-N-methylcyclopentanamine B)N-Cyclohexyl-N-methylcyclopentanamine C)N-Cyclopentyl-N-methylcyclohexanamine D)Dicyclopentylmethylamine E)N-Pentyl-N-methylpentanamine <div style=padding-top: 35px>

A)N-Cyclopentyl-N-methylcyclopentanamine
B)N-Cyclohexyl-N-methylcyclopentanamine
C)N-Cyclopentyl-N-methylcyclohexanamine
D)Dicyclopentylmethylamine
E)N-Pentyl-N-methylpentanamine
Question
What type of amine is pyridine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
Which of these is properly termed a "quaternary ammonium salt"?

A)(CH3)3CCH2CH2NH3+ Cl-
B)(CH3CH2CH(CH3)CH2)2NH2+ Cl-
C)(CH3CH2CH2)3NH+ Cl-
D)(CH3CH2CH2)4N+ Cl-
E)None of these choices.
Question
The aromatic amine purine contains how many nitrogen atoms?

A)1
B)2
C)3
D)4
E)5
Question
Which is a correct IUPAC name for the following substance? <strong>Which is a correct IUPAC name for the following substance?  </strong> A)N-Ethylhexanamine B)N-Ethylcyclohexanamine C)N-Cyclohexylethanamine D)N-Ethylcyclopentanamine E)N-Ethylaniline <div style=padding-top: 35px>

A)N-Ethylhexanamine
B)N-Ethylcyclohexanamine
C)N-Cyclohexylethanamine
D)N-Ethylcyclopentanamine
E)N-Ethylaniline
Question
Which of these is an acceptable alternative name to "(1-methylbutyl)amine"?

A)2-Aminopentane
B)2-Pentanamine
C)Isopentylamine
D)sec-Pentylamine
E)Both 2-aminopentane and 2-pentanamine
Question
What type of amine is indole?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
What type of amine is N-methylmorpholine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
What type of amine is N-methyl-2-methyl-3-hexanamine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
Which of the following is a tertiary amine?

A)CH3CH2CH2CH2NH2
B)CH3CH2NHCH2CH(CH3)2
C)(CH3CH2)2NCH2CH(CH3)2
D)(CH3CH2)4N+ OH-
E)(CH3CH2)3CNH2
Question
The aromatic amine imidazole contains how many nitrogen atoms?

A)1
B)2
C)3
D)4
E)5
Question
What type of amine is pyrrolidine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
Question
Which of these alkyl halides cannot be used effectively in a Gabriel amine synthesis?

A)1-bromopentane
B)1-bromo-3-methylbutane
C)2-bromo-3-methylpentane
D)1-bromo-2,3-dimethylbutane
E)2-bromo-2,3-dimethylbutane
Question
Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, δ\delta 1.0
Quartet, δ\delta 2.5
Singlet, δ\delta 3.6 (2H)
Multiplet, δ\delta 7.3 (5H)
The most likely structure for W is:

A)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which reagent will distinguish between 2-amino-2,3-dimethylpentane and 1-amino-3-methyl-2-pentene?

A)HONO,0-5 °C
B)C6H5SO2Cl/OH-,then H3O+
C)NaOH
D)HCl
E)Br2/CCl4
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
The reaction of which of these compounds with nitrous acid results in a stable N-nitroso compound?

A)C6H5NH2
B)C6H5N(CH3)2
C)CH3CH2CH2CH2CH2NH2
D)C6H5NHCH3
E)CH3CH2CONH2
Question
This type of compound is the only one of these which can be converted by reduction into a 1 \circ ,2 \circ or 3 \circ amine,according to its particular structure:

A)Nitrile
B)Oxime
C)Azide
D)Amide
E)Nitroalkane
Question
The correct structure of (R)-N-methylbicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (R)-N-methylbicyclo[2.2.1]heptan-2-amine is?  </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
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
When the process ArNH2 \to ArY is carried out via an intermediate diazonium salt,this salt is isolated only in the case in which Y is which of these groups?

A)-F
B)-Cl
C)-Br
D)-I
E)-CN
Question
Which of the following compounds would be the strongest base? <strong>Which of the following compounds would be the strongest base?  </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
What is the basis for the successful resolution of racemic C6H5CHOHCO2H through use of the chiral amine,C6H5CH(NH2)CH3?

A)One enantiomer is more soluble than the other.
B)The racemic mixture is converted into a single isomer in the basic solvent.
C)The diastereomeric salts formed have different solubilities.
D)The diastereomeric salts have different boiling points.
E)The diastereomeric salts have different melting points.
Question
Which of these compounds is expected to possess the lowest boiling point?

A)CH3CH2CH2CH2CH2NH2
B)CH3CH2CH2NHCH2CH3
C)(CH3CH2)2NCH3
D)(CH3CH2)2CHOH
E)(CH3)3CCH2NH3+ Cl-
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
Question
Which is not an intermediate in the Hofmann degradation reaction? <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)   <div style=padding-top: 35px>

A)RN=C=O
B) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which reagent could be used to separate a mixture of aniline and toluene?

A)KMnO4 in H2O
B)Dilute NaOH
C)Dilute NaHCO3
D)Ag(NH3)2OH
E)Dilute HCl
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)Tollens' test B)Dilute NaHCO<sub>3</sub> C)Hinsberg test D)Iodoform test E)None of these choices. <div style=padding-top: 35px>

A)Tollens' test
B)Dilute NaHCO3
C)Hinsberg test
D)Iodoform test
E)None of these choices.
Question
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)HONO,0-5 °C then  \beta -naphthol C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl and OH<sup>-</sup> in H<sub>2</sub>O E)Dilute HCl <div style=padding-top: 35px>

A)AgNO3 in H2O
B)HONO,0-5 °C then β\beta -naphthol
C)Dilute NaOH
D)C6H5SO2Cl and OH- in H2O
E)Dilute HCl
Question
Which of the following aryl amines is the strongest base?

A)Aniline
B)p-Trimethylammonium aniline
C)p-Methoxyaniline
D)p-Trifluoromethylaniline
E)p-Chloroaniline
Question
Which of the following bases has a conjugate acid with the smallest pKa?

A)p-Methylaniline
B)p-Methoxyaniline
C)Hexylamine
D)p-Nitroaniline
E)Dipropylamine
Question
Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)II < I < III < IV D)II < III < I < IV E)Cannot be determined from information given <div style=padding-top: 35px>

A)IV < II < I < III
B)III < II < IV < I
C)II < I < III < IV
D)II < III < I < IV
E)Cannot be determined from information given
Question
Which of these would be predicted to have the largest pKa? <strong>Which of these would be predicted to have the largest pK<sub>a</sub>?  </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
Which of these is the weakest acid? <strong>Which of these is the weakest acid?  </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
Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)II < I < III < IV D)II < III < I < IV E)Cannot be determined from information given <div style=padding-top: 35px>

A)IV < II < I < III
B)III < II < IV < I
C)II < I < III < IV
D)II < III < I < IV
E)Cannot be determined from information given
Question
Arrange the following amines in order of decreasing basicity (most to least)in aqueous solution: <strong>Arrange the following amines in order of decreasing basicity (most to least)in aqueous solution:  </strong> A)IV > II > I > III B)III > II > IV > I C)III > I > II > IV D)II > III > I > IV E)Cannot be determined from information given <div style=padding-top: 35px>

A)IV > II > I > III
B)III > II > IV > I
C)III > I > II > IV
D)II > III > I > IV
E)Cannot be determined from information given
Question
Which of these would be predicted to have the smallest pKa? <strong>Which of these would be predicted to have the smallest pK<sub>a</sub>?  </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
Which of the following compounds would be the weakest base? <strong>Which of the following compounds would be the weakest base?  </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
Which of the following compounds would be the strongest base? <strong>Which of the following compounds would be the strongest base?  </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
Which of the following bases has a conjugate acid with the smallest pKa? <strong>Which of the following bases has a conjugate acid with the smallest pK<sub>a</sub>?  </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
Which of the following bases has a conjugate acid with the largest pKa? <strong>Which of the following bases has a conjugate acid with the largest pK<sub>a</sub>?  </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
Which of the following aryl amines is the weakest base?

A)Aniline
B)p-Trimethylammonium aniline
C)p-Methoxyaniline
D)p-Trifluoromethylaniline
E)p-Chloroaniline
Question
Which would be the weakest base?

A)p-Methylaniline
B)p-Methoxyaniline
C)Hexylamine
D)p-Nitroaniline
E)Dipropylamine
Question
In aqueous solution,which of the following bases has the conjugate acid that possesses the smallest value for pKa?

A)C6H5NH2
B)NH3
C)(CH3CH2)3N
D)(CH3CH2)2NH
E)CH3CH2CH2NH2
Question
Which of these is the strongest acid? <strong>Which of these is the strongest acid?  </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
Which of the following bases has a conjugate acid with the smallest pKa? <strong>Which of the following bases has a conjugate acid with the smallest pK<sub>a</sub>?  </strong> A)I B)II C)III D)IV E)Cannot be determined from information given <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)Cannot be determined from information given
Question
Which of these is the strongest acid? <strong>Which of these is the strongest acid?  </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
Arrange the following amines in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following amines in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)III < I < II < IV D)II < III < I < IV E)Cannot be determined from information given <div style=padding-top: 35px>

A)IV < II < I < III
B)III < II < IV < I
C)III < I < II < IV
D)II < III < I < IV
E)Cannot be determined from information given
Question
Which of these compounds is soluble in dilute sodium hydroxide solution? <strong>Which of these compounds is soluble in dilute sodium hydroxide solution?  </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 best method(s)to prepare <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> .

A) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
B) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
C)
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
D) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
E) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
Question
Which of the following can be used to prepare allylamine (pure)? <strong>Which of the following can be used to prepare allylamine (pure)?  </strong> A)I B)II C)III D)I and II E)II and III <div style=padding-top: 35px>

A)I
B)II
C)III
D)I and II
E)II and III
Question
Which of the following can be used to prepare benzylamine (pure)? <strong>Which of the following can be used to prepare benzylamine (pure)?  </strong> A)I B)II C)III D)I and II E)II and III <div style=padding-top: 35px>

A)I
B)II
C)III
D)I and II
E)II and III
Question
Consider the synthesis below.What is reagent A? <strong>Consider the synthesis below.What is reagent A?  </strong> A)H<sub>3</sub>PO<sub>2</sub> B)HCN C)P<sub>4</sub>O<sub>10</sub> D)CuCN E)CuCl<sub>2</sub> <div style=padding-top: 35px>

A)H3PO2
B)HCN
C)P4O10
D)CuCN
E)CuCl2
Question
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
Question
What reagent can effect the following transformation? <strong>What reagent can effect the following transformation?  </strong> A)Sn/HCl; then OH<sup>-</sup> B)NH<sub>2</sub>Cl C)H<sub>3</sub>PO<sub>2</sub> D)CuCN E)HONO; then NH<sub>3</sub> <div style=padding-top: 35px>

A)Sn/HCl; then OH-
B)NH2Cl
C)H3PO2
D)CuCN
E)HONO; then NH3
Question
Which is the best method to prepare 1-phenylethanamine?

A) <strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
Question
Consider the synthesis below.What is compound B? <strong>Consider the synthesis below.What is compound B?    </strong> A)I B)II C)III D)IV E)V <div style=padding-top: 35px> <strong>Consider the synthesis below.What is compound B?    </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
What reagent can effect the following transformation? <strong>What reagent can effect the following transformation?  </strong> A)Fe/HCl; then OH<sup>-</sup> B)NH<sub>2</sub>Cl C)H<sub>3</sub>PO<sub>2</sub> D)CuCN E)HONO; then NH<sub>3</sub> <div style=padding-top: 35px>

A)Fe/HCl; then OH-
B)NH2Cl
C)H3PO2
D)CuCN
E)HONO; then NH3
Question
Which is the best method to prepare <strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> ?

A) <strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Consider the synthesis below.What is reagent "Y"? <strong>Consider the synthesis below.What is reagent Y?  </strong> A)Br<sub>2</sub>/FeBr<sub>3</sub> B)CuBr C)CuBr<sub>2</sub> D)H<sub>3</sub>PO<sub>2</sub>/H<sub>2</sub>O E)H<sub>3</sub>PO<sub>4</sub> <div style=padding-top: 35px>

A)Br2/FeBr3
B)CuBr
C)CuBr2
D)H3PO2/H2O
E)H3PO4
Question
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px> and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   <div style=padding-top: 35px>
Question
Which is the best method to prepare 1-phenylethanamine?

A) <strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following reactions would yield C6H5CH2NH2?

A)
<strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices. <div style=padding-top: 35px>
B) <strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices. <div style=padding-top: 35px>
C)
<strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices. <div style=padding-top: 35px>
D)All of these choices.
E)Two of these choices.
Question
Consider the synthesis below.What is reagent A? <strong>Consider the synthesis below.What is reagent A?  </strong> A)Br<sub>2</sub>,FeBr<sub>3</sub> B)Fe,HCl; then OH<sup>-</sup> C)NH<sub>2</sub>Cl,AlCl<sub>3</sub> D)H<sub>3</sub>PO<sub>2</sub> E)LiNH<sub>2</sub> <div style=padding-top: 35px>

A)Br2,FeBr3
B)Fe,HCl; then OH-
C)NH2Cl,AlCl3
D)H3PO2
E)LiNH2
Question
Consider the synthesis below.What is reagent "Z"? <strong>Consider the synthesis below.What is reagent Z?  </strong> A)CuCl B)CuCl<sub>2</sub> C)NaCl D)KCl E)HCl/heat <div style=padding-top: 35px>

A)CuCl
B)CuCl2
C)NaCl
D)KCl
E)HCl/heat
Question
Which of these could be resolved into separate enantiomers?

A)4-Methyl-1-pentanamine
B)4-Methyl-2-pentanamine
C)N-Methyl-1-butanamine
D)N,N-Dimethyl-1-propanamine
E)N-Butyltrimethylammonium bromide
Question
Consider the synthesis below.What is reagent C? <strong>Consider the synthesis below.What is reagent C?  </strong> A)excess Br<sub>2</sub>,H<sub>2</sub>O B)Fe,HCl; then OH<sup>-</sup> C)NH<sub>2</sub>Cl,AlCl<sub>3</sub> D)CuBr E)HNO<sub>3</sub>,H<sub>2</sub>SO<sub>4</sub>,Fe <div style=padding-top: 35px>

A)excess Br2,H2O
B)Fe,HCl; then OH-
C)NH2Cl,AlCl3
D)CuBr
E)HNO3,H2SO4,Fe
Question
Which of the following can be used to prepare 2-aminopentane (pure)? <strong>Which of the following can be used to prepare 2-aminopentane (pure)?  </strong> A)I B)II C)III D)I and II E)II and III <div style=padding-top: 35px>

A)I
B)II
C)III
D)I and II
E)II and III
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Deck 20: Amines
1
The correct structure of (S)-bicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (S)-bicyclo[2.2.1]heptan-2-amine is?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
III
2
The correct structure of bicyclo[1.1.0]butan-1-amine is? <strong>The correct structure of bicyclo[1.1.0]butan-1-amine is?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
II
3
The correct structure of (S)-N-methylbicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (S)-N-methylbicyclo[2.2.1]heptan-2-amine is?  </strong> A)I B)II C)III D)IV E)V

A)I
B)II
C)III
D)IV
E)V
III
4
Which is a correct common name for the following substance? <strong>Which is a correct common name for the following substance?  </strong> A)Ethylethylisobutylamine B)Diethylisobutylamine C)sec-Butyldiethylamine D)Ethylethyl-sec-butylamine E)2-Diethylaminobutane

A)Ethylethylisobutylamine
B)Diethylisobutylamine
C)sec-Butyldiethylamine
D)Ethylethyl-sec-butylamine
E)2-Diethylaminobutane
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5
What type of amine is piperidine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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6
What type of amine is quinoline?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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7
What type of amine is pyrrole?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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8
The correct structure of bicyclo[1.1.0]butan-2-amine is? <strong>The correct structure of bicyclo[1.1.0]butan-2-amine is?  </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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9
Which is a correct IUPAC name for the following substance? <strong>Which is a correct IUPAC name for the following substance?  </strong> A)N-Cyclopentyl-N-methylcyclopentanamine B)N-Cyclohexyl-N-methylcyclopentanamine C)N-Cyclopentyl-N-methylcyclohexanamine D)Dicyclopentylmethylamine E)N-Pentyl-N-methylpentanamine

A)N-Cyclopentyl-N-methylcyclopentanamine
B)N-Cyclohexyl-N-methylcyclopentanamine
C)N-Cyclopentyl-N-methylcyclohexanamine
D)Dicyclopentylmethylamine
E)N-Pentyl-N-methylpentanamine
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10
What type of amine is pyridine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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11
Which of these is properly termed a "quaternary ammonium salt"?

A)(CH3)3CCH2CH2NH3+ Cl-
B)(CH3CH2CH(CH3)CH2)2NH2+ Cl-
C)(CH3CH2CH2)3NH+ Cl-
D)(CH3CH2CH2)4N+ Cl-
E)None of these choices.
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12
The aromatic amine purine contains how many nitrogen atoms?

A)1
B)2
C)3
D)4
E)5
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13
Which is a correct IUPAC name for the following substance? <strong>Which is a correct IUPAC name for the following substance?  </strong> A)N-Ethylhexanamine B)N-Ethylcyclohexanamine C)N-Cyclohexylethanamine D)N-Ethylcyclopentanamine E)N-Ethylaniline

A)N-Ethylhexanamine
B)N-Ethylcyclohexanamine
C)N-Cyclohexylethanamine
D)N-Ethylcyclopentanamine
E)N-Ethylaniline
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14
Which of these is an acceptable alternative name to "(1-methylbutyl)amine"?

A)2-Aminopentane
B)2-Pentanamine
C)Isopentylamine
D)sec-Pentylamine
E)Both 2-aminopentane and 2-pentanamine
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15
What type of amine is indole?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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16
What type of amine is N-methylmorpholine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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17
What type of amine is N-methyl-2-methyl-3-hexanamine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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18
Which of the following is a tertiary amine?

A)CH3CH2CH2CH2NH2
B)CH3CH2NHCH2CH(CH3)2
C)(CH3CH2)2NCH2CH(CH3)2
D)(CH3CH2)4N+ OH-
E)(CH3CH2)3CNH2
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19
The aromatic amine imidazole contains how many nitrogen atoms?

A)1
B)2
C)3
D)4
E)5
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20
What type of amine is pyrrolidine?

A)Primary
B)Secondary
C)Tertiary
D)Quaternary
E)None of these choices.
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21
Which of these alkyl halides cannot be used effectively in a Gabriel amine synthesis?

A)1-bromopentane
B)1-bromo-3-methylbutane
C)2-bromo-3-methylpentane
D)1-bromo-2,3-dimethylbutane
E)2-bromo-2,3-dimethylbutane
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22
Compound W has the molecular formula C11H17N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The 1H NMR spectrum of W consists of: triplet, δ\delta 1.0
Quartet, δ\delta 2.5
Singlet, δ\delta 3.6 (2H)
Multiplet, δ\delta 7.3 (5H)
The most likely structure for W is:

A)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)
B)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)
C)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)
D)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)
E)  <strong>Compound W has the molecular formula C<sub>11</sub>H<sub>17</sub>N.Treatment of W with benzenesulfonyl chloride in base gives no reaction.Acidification of the resulting mixture gives a clear solution.The <sup>1</sup>H NMR spectrum of W consists of: triplet, \delta  1.0 Quartet, \delta   2.5 Singlet, \delta   3.6 (2H) Multiplet, \delta   7.3 (5H) The most likely structure for W is:</strong> A)   B)   C)   D)   E)
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23
Which reagent will distinguish between 2-amino-2,3-dimethylpentane and 1-amino-3-methyl-2-pentene?

A)HONO,0-5 °C
B)C6H5SO2Cl/OH-,then H3O+
C)NaOH
D)HCl
E)Br2/CCl4
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24
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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25
The reaction of which of these compounds with nitrous acid results in a stable N-nitroso compound?

A)C6H5NH2
B)C6H5N(CH3)2
C)CH3CH2CH2CH2CH2NH2
D)C6H5NHCH3
E)CH3CH2CONH2
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26
This type of compound is the only one of these which can be converted by reduction into a 1 \circ ,2 \circ or 3 \circ amine,according to its particular structure:

A)Nitrile
B)Oxime
C)Azide
D)Amide
E)Nitroalkane
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27
The correct structure of (R)-N-methylbicyclo[2.2.1]heptan-2-amine is? <strong>The correct structure of (R)-N-methylbicyclo[2.2.1]heptan-2-amine is?  </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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28
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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29
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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30
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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31
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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32
When the process ArNH2 \to ArY is carried out via an intermediate diazonium salt,this salt is isolated only in the case in which Y is which of these groups?

A)-F
B)-Cl
C)-Br
D)-I
E)-CN
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33
Which of the following compounds would be the strongest base? <strong>Which of the following compounds would be the strongest base?  </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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34
What is the basis for the successful resolution of racemic C6H5CHOHCO2H through use of the chiral amine,C6H5CH(NH2)CH3?

A)One enantiomer is more soluble than the other.
B)The racemic mixture is converted into a single isomer in the basic solvent.
C)The diastereomeric salts formed have different solubilities.
D)The diastereomeric salts have different boiling points.
E)The diastereomeric salts have different melting points.
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35
Which of these compounds is expected to possess the lowest boiling point?

A)CH3CH2CH2CH2CH2NH2
B)CH3CH2CH2NHCH2CH3
C)(CH3CH2)2NCH3
D)(CH3CH2)2CHOH
E)(CH3)3CCH2NH3+ Cl-
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36
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)Dilute NaHCO<sub>3</sub> C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl/OH<sup>-</sup>,then H<sub>3</sub>O<sup>+</sup> E)Dilute HCl

A)AgNO3 in H2O
B)Dilute NaHCO3
C)Dilute NaOH
D)C6H5SO2Cl/OH-,then H3O+
E)Dilute HCl
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37
Which is not an intermediate in the Hofmann degradation reaction? <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)

A)RN=C=O
B) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)
C) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)
D) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)
E) <strong>Which is not an intermediate in the Hofmann degradation reaction?  </strong> A)RN=C=O B)   C)   D)   E)
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38
Which reagent could be used to separate a mixture of aniline and toluene?

A)KMnO4 in H2O
B)Dilute NaOH
C)Dilute NaHCO3
D)Ag(NH3)2OH
E)Dilute HCl
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39
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below? <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)Tollens' test B)Dilute NaHCO<sub>3</sub> C)Hinsberg test D)Iodoform test E)None of these choices.

A)Tollens' test
B)Dilute NaHCO3
C)Hinsberg test
D)Iodoform test
E)None of these choices.
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40
Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  <strong>Which reagent would serve as the basis for a simple chemical test that would distinguish between the pair of compounds listed below?  </strong> A)AgNO<sub>3</sub> in H<sub>2</sub>O B)HONO,0-5 °C then  \beta -naphthol C)Dilute NaOH D)C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl and OH<sup>-</sup> in H<sub>2</sub>O E)Dilute HCl

A)AgNO3 in H2O
B)HONO,0-5 °C then β\beta -naphthol
C)Dilute NaOH
D)C6H5SO2Cl and OH- in H2O
E)Dilute HCl
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41
Which of the following aryl amines is the strongest base?

A)Aniline
B)p-Trimethylammonium aniline
C)p-Methoxyaniline
D)p-Trifluoromethylaniline
E)p-Chloroaniline
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42
Which of the following bases has a conjugate acid with the smallest pKa?

A)p-Methylaniline
B)p-Methoxyaniline
C)Hexylamine
D)p-Nitroaniline
E)Dipropylamine
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43
Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)II < I < III < IV D)II < III < I < IV E)Cannot be determined from information given

A)IV < II < I < III
B)III < II < IV < I
C)II < I < III < IV
D)II < III < I < IV
E)Cannot be determined from information given
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44
Which of these would be predicted to have the largest pKa? <strong>Which of these would be predicted to have the largest pK<sub>a</sub>?  </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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45
Which of these is the weakest acid? <strong>Which of these is the weakest acid?  </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
Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following compounds in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)II < I < III < IV D)II < III < I < IV E)Cannot be determined from information given

A)IV < II < I < III
B)III < II < IV < I
C)II < I < III < IV
D)II < III < I < IV
E)Cannot be determined from information given
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47
Arrange the following amines in order of decreasing basicity (most to least)in aqueous solution: <strong>Arrange the following amines in order of decreasing basicity (most to least)in aqueous solution:  </strong> A)IV > II > I > III B)III > II > IV > I C)III > I > II > IV D)II > III > I > IV E)Cannot be determined from information given

A)IV > II > I > III
B)III > II > IV > I
C)III > I > II > IV
D)II > III > I > IV
E)Cannot be determined from information given
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48
Which of these would be predicted to have the smallest pKa? <strong>Which of these would be predicted to have the smallest pK<sub>a</sub>?  </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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49
Which of the following compounds would be the weakest base? <strong>Which of the following compounds would be the weakest base?  </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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50
Which of the following compounds would be the strongest base? <strong>Which of the following compounds would be the strongest base?  </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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51
Which of the following bases has a conjugate acid with the smallest pKa? <strong>Which of the following bases has a conjugate acid with the smallest pK<sub>a</sub>?  </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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52
Which of the following bases has a conjugate acid with the largest pKa? <strong>Which of the following bases has a conjugate acid with the largest pK<sub>a</sub>?  </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
Which of the following aryl amines is the weakest base?

A)Aniline
B)p-Trimethylammonium aniline
C)p-Methoxyaniline
D)p-Trifluoromethylaniline
E)p-Chloroaniline
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54
Which would be the weakest base?

A)p-Methylaniline
B)p-Methoxyaniline
C)Hexylamine
D)p-Nitroaniline
E)Dipropylamine
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55
In aqueous solution,which of the following bases has the conjugate acid that possesses the smallest value for pKa?

A)C6H5NH2
B)NH3
C)(CH3CH2)3N
D)(CH3CH2)2NH
E)CH3CH2CH2NH2
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56
Which of these is the strongest acid? <strong>Which of these is the strongest acid?  </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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57
Which of the following bases has a conjugate acid with the smallest pKa? <strong>Which of the following bases has a conjugate acid with the smallest pK<sub>a</sub>?  </strong> A)I B)II C)III D)IV E)Cannot be determined from information given

A)I
B)II
C)III
D)IV
E)Cannot be determined from information given
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58
Which of these is the strongest acid? <strong>Which of these is the strongest acid?  </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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59
Arrange the following amines in order of increasing basicity (least to most)in aqueous solution: <strong>Arrange the following amines in order of increasing basicity (least to most)in aqueous solution:  </strong> A)IV < II < I < III B)III < II < IV < I C)III < I < II < IV D)II < III < I < IV E)Cannot be determined from information given

A)IV < II < I < III
B)III < II < IV < I
C)III < I < II < IV
D)II < III < I < IV
E)Cannot be determined from information given
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60
Which of these compounds is soluble in dilute sodium hydroxide solution? <strong>Which of these compounds is soluble in dilute sodium hydroxide solution?  </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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61
Identify the best method(s)to prepare <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   .

A) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and
B) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and
C)
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and
D) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and
E) <strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare   .</strong> A)   B)   C)   D)   and   E)   and
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62
Which of the following can be used to prepare allylamine (pure)? <strong>Which of the following can be used to prepare allylamine (pure)?  </strong> A)I B)II C)III D)I and II E)II and III

A)I
B)II
C)III
D)I and II
E)II and III
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63
Which of the following can be used to prepare benzylamine (pure)? <strong>Which of the following can be used to prepare benzylamine (pure)?  </strong> A)I B)II C)III D)I and II E)II and III

A)I
B)II
C)III
D)I and II
E)II and III
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64
Consider the synthesis below.What is reagent A? <strong>Consider the synthesis below.What is reagent A?  </strong> A)H<sub>3</sub>PO<sub>2</sub> B)HCN C)P<sub>4</sub>O<sub>10</sub> D)CuCN E)CuCl<sub>2</sub>

A)H3PO2
B)HCN
C)P4O10
D)CuCN
E)CuCl2
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65
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
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66
What reagent can effect the following transformation? <strong>What reagent can effect the following transformation?  </strong> A)Sn/HCl; then OH<sup>-</sup> B)NH<sub>2</sub>Cl C)H<sub>3</sub>PO<sub>2</sub> D)CuCN E)HONO; then NH<sub>3</sub>

A)Sn/HCl; then OH-
B)NH2Cl
C)H3PO2
D)CuCN
E)HONO; then NH3
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67
Which is the best method to prepare 1-phenylethanamine?

A) <strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
B)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
C)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
D)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
E)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
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68
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
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69
Consider the synthesis below.What is compound B? <strong>Consider the synthesis below.What is compound B?    </strong> A)I B)II C)III D)IV E)V <strong>Consider the synthesis below.What is compound B?    </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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70
What reagent can effect the following transformation? <strong>What reagent can effect the following transformation?  </strong> A)Fe/HCl; then OH<sup>-</sup> B)NH<sub>2</sub>Cl C)H<sub>3</sub>PO<sub>2</sub> D)CuCN E)HONO; then NH<sub>3</sub>

A)Fe/HCl; then OH-
B)NH2Cl
C)H3PO2
D)CuCN
E)HONO; then NH3
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71
Which is the best method to prepare <strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)   ?

A) <strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)
B)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)
C)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)
D)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)
E)
<strong>Which is the best method to prepare   ?</strong> A)   B)   C)   D)   E)
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72
Consider the synthesis below.What is reagent "Y"? <strong>Consider the synthesis below.What is reagent Y?  </strong> A)Br<sub>2</sub>/FeBr<sub>3</sub> B)CuBr C)CuBr<sub>2</sub> D)H<sub>3</sub>PO<sub>2</sub>/H<sub>2</sub>O E)H<sub>3</sub>PO<sub>4</sub>

A)Br2/FeBr3
B)CuBr
C)CuBr2
D)H3PO2/H2O
E)H3PO4
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73
Identify the best method(s)to prepare N-methylphenylmethanamine.

A) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
B) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
C)
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
D) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
E) <strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and   and
<strong>Identify the best method(s)to prepare N-methylphenylmethanamine.</strong> A)   B)   C)   D)   and   E)   and
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74
Which is the best method to prepare 1-phenylethanamine?

A) <strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
B)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
C)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
D)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
E)
<strong>Which is the best method to prepare 1-phenylethanamine?</strong> A)   B)   C)   D)   E)
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75
Which of the following reactions would yield C6H5CH2NH2?

A)
<strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices.
B) <strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices.
C)
<strong>Which of the following reactions would yield C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>NH<sub>2</sub>?</strong> A)   B)   C)   D)All of these choices. E)Two of these choices.
D)All of these choices.
E)Two of these choices.
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76
Consider the synthesis below.What is reagent A? <strong>Consider the synthesis below.What is reagent A?  </strong> A)Br<sub>2</sub>,FeBr<sub>3</sub> B)Fe,HCl; then OH<sup>-</sup> C)NH<sub>2</sub>Cl,AlCl<sub>3</sub> D)H<sub>3</sub>PO<sub>2</sub> E)LiNH<sub>2</sub>

A)Br2,FeBr3
B)Fe,HCl; then OH-
C)NH2Cl,AlCl3
D)H3PO2
E)LiNH2
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77
Consider the synthesis below.What is reagent "Z"? <strong>Consider the synthesis below.What is reagent Z?  </strong> A)CuCl B)CuCl<sub>2</sub> C)NaCl D)KCl E)HCl/heat

A)CuCl
B)CuCl2
C)NaCl
D)KCl
E)HCl/heat
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78
Which of these could be resolved into separate enantiomers?

A)4-Methyl-1-pentanamine
B)4-Methyl-2-pentanamine
C)N-Methyl-1-butanamine
D)N,N-Dimethyl-1-propanamine
E)N-Butyltrimethylammonium bromide
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79
Consider the synthesis below.What is reagent C? <strong>Consider the synthesis below.What is reagent C?  </strong> A)excess Br<sub>2</sub>,H<sub>2</sub>O B)Fe,HCl; then OH<sup>-</sup> C)NH<sub>2</sub>Cl,AlCl<sub>3</sub> D)CuBr E)HNO<sub>3</sub>,H<sub>2</sub>SO<sub>4</sub>,Fe

A)excess Br2,H2O
B)Fe,HCl; then OH-
C)NH2Cl,AlCl3
D)CuBr
E)HNO3,H2SO4,Fe
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80
Which of the following can be used to prepare 2-aminopentane (pure)? <strong>Which of the following can be used to prepare 2-aminopentane (pure)?  </strong> A)I B)II C)III D)I and II E)II and III

A)I
B)II
C)III
D)I and II
E)II and III
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Unlock for access to all 207 flashcards in this deck.