Deck 11: Amines and Related Nitrogen Compounds

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Question
Which compound is the strongest base?

A) CH3NH2
B) CH3CO2H
C) CH3CHO
D) CH3OH
E) C6H5NH2
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Question
The mechanism by which acylation of an amine with an acid chloride takes place is:

A) nucleophilic acyl substitution
B) electrophilic aromatic substitution
C) nucleophilic addition
D) electrophilic addition
E) nucleophilic aromatic substitution
Question
Which of the following compounds is a tertiary amine?

A) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The structure below can be named in the following manner: <strong>The structure below can be named in the following manner:  </strong> A) 2-nitrocyclohexanamine B) m-nitroaniline C) o-nitroaniline D) 2-nitrobenzylamine E) 1,2-diaminobenzene <div style=padding-top: 35px>

A) 2-nitrocyclohexanamine
B) m-nitroaniline
C) o-nitroaniline
D) 2-nitrobenzylamine
E) 1,2-diaminobenzene
Question
Which of the following are tertiary amines? <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <div style=padding-top: 35px> <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <div style=padding-top: 35px> <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <div style=padding-top: 35px> <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <div style=padding-top: 35px> <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <div style=padding-top: 35px>

A) 1 and 3
B) only 5
C) 1, 2, 3, and 4
D) 2 and 4
E) 1 and 2
Question
Which of the following amines is the most basic?

A) methylamine
B) dimethylamine
C) ammonia
D) aniline
E) N-methylaniline
Question
What is the mechanism for the intramolecular alkylation shown below?
<strong>What is the mechanism for the intramolecular alkylation shown below?  </strong> A) S<sub>N</sub>2 B) S<sub>N</sub>1 C) nucleophilic acyl substitution D) nucleophilic addition E) electrophilic addition <div style=padding-top: 35px>

A) SN2
B) SN1
C) nucleophilic acyl substitution
D) nucleophilic addition
E) electrophilic addition
Question
C6H5NHCH2CH2CH3 can best be prepared as follows:

A) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following is not an intermediate in the diazotization of aniline using nitrous acid? <strong>Which of the following is not an intermediate in the diazotization of aniline using nitrous acid?  </strong> A) I B) II C) III D) IV E) none of the above <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) none of the above
Question
When methylamine (CH3NH2) reacts with methyl bromide (CH3Br) to give dimethylamine, the methylamine:

A) acts as an electrophile
B) acts as a Lewis acid
C) acts as a Bronsted-Lowry acid
D) acts as a Bronsted-Lowry base
E) acts as a nucleophile in an SN2 reaction
Question
The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is

A) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
To separate a mixture of p-toluidine and p-nitrotoluene dissolved in ether,

A) extract the ether solution with aqueous HCl and treat the water layer with aqueous NaOH.
B) extract the ether solution with aqueous NaOH and treat the water layer with aqueous HCl.
C) extract the ether solution with water and treat the water layer with aqueous NaOH.
D) extract the ether layer with aqueous HCl and treat the ether layer with aqueous NaOH.
E) extract the ether solution with aqueous HCl and treat the ether layer with aqueous HCl.
Question
Tert-butylamine is classified as a(n) amine.

A) 1°
B) 2°
C) 3°
D) quaternary salt
E) aromatic
Question
The alkylation of an amine with an alkyl halide takes place by the following mechanism:

A) SN1
B) SN2
C) electrophilic addition
D) E1
E) E2
Question
The order of decreasing pKas of the corresponding ammonium ions of the following is: <strong>The order of decreasing pK<sub>a</sub>s of the corresponding ammonium ions of the following is:  </strong> A) 1 > 2 > 3 > 4 B) 3 > 4 > 2 > 1 C) 4 > 3 > 2 > 1 D) 2 > 1 > 3 > 4 E) 4 > 3 > 1 > 2 <div style=padding-top: 35px>

A) 1 > 2 > 3 > 4
B) 3 > 4 > 2 > 1
C) 4 > 3 > 2 > 1
D) 2 > 1 > 3 > 4
E) 4 > 3 > 1 > 2
Question
The order of increasing basicity of the following is: <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <div style=padding-top: 35px>
<strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <div style=padding-top: 35px> <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <div style=padding-top: 35px> <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <div style=padding-top: 35px>

A) 1 < 2 < 3 < 4
B) 2 < 3 < 1 < 4
C) 4 < 3 < 2 < 1
D) 4 < 3 < 1 < 2
E) 4 < 1 < 3 < 2
Question
The order of decreasing acidity of the following is: <strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1 <div style=padding-top: 35px>
<strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1 <div style=padding-top: 35px>
<strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 3 > 1 > 2
C) 2 > 1 > 3
D) 3 > 2 > 1
E) 2 > 3 > 1
Question
What structure represents a cationic intermediate in the electrophilic aromatic bromination of aniline? <strong>What structure represents a cationic intermediate in the electrophilic aromatic bromination of aniline?  </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 molecules has the highest boiling point?

A) ethylamine
B) propane
C) ethyl alcohol
D) dimethyl ether
E) acetaldehyde
Question
Which of the following statements is false:

A) Aliphatic 3o amines with three different groups on nitrogen can be resolved.
B) Primary and secondary aliphatic amines can be hydrogen bond donors.
C) Aliphatic amines can be hydrogen bond acceptors.
D) The non-bonded lone pair in an aliphatic amine is more basic than the non-bonded lone pairs in ethers.
E) The nitrogen in aliphatic amines is sp3-hybridized.
Question
What type of products are formed by diazo coupling reactions?

A) meso compounds
B) azo compounds
C) diazonium salts
D) quaternary ammonium salts
E) racemic mixtures
Question
Aniline <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> is best prepared via:

A) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What reacts with benzenediazonium chloride to produce benzonitrile?

A) HONO
B) Li, NH3
C) NaBH3CN
D) KCN, Cu2CN2
E) LiAlH4, ether
Question
What is the name of the product formed by reacting CuCl and HCl with benzenediazonium chloride?

A) bromobenzene
B) chlorobenzene
C) o-chloroaniline
D) m-chloroaniline
E) p-chloroaniline
Question
The reaction of a 2o amine with nitrous acid gives:

A) a quaternary ammonium salt
B) a nitrosamine
C) A diazonium salt
D) an azo dye
E) a nitro compound
Question
Reacting aniline, C6H5NH2, with a primary alkyl halide will produce a(n):

A) 1° amine
B) 2° amine
C) 3° amine
D) amide
E) imine
Question
The product(s) of <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px> are:

A) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
m-Dichlorobenzene can be prepared in good yield by the sequence:

A) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What is the final product for the following sequence of reactions?
<strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What is the stereochemical relationship of the products formed by reacting racemic lactic acid with (S)-1-phenylethylamine?

A) enantiomers
B) meso compounds
C) racemic mixture
D) diastereomers
E) geometric isomers
Question
The amines that can be acylated by acetic anhydride are <strong>The amines that can be acylated by acetic anhydride are  </strong> A) only 4 B) 1, 2, 3, and 4 C) 1 and 3 D) 2 and 4 E) only 2 <div style=padding-top: 35px>

A) only 4
B) 1, 2, 3, and 4
C) 1 and 3
D) 2 and 4
E) only 2
Question
What is the name of the product of the following reaction? <strong>What is the name of the product of the following reaction?  </strong> A) chlorobenzene B) chloroaniline C) anilinium chloride D) o-chloroaniline E) N-chloroaniline <div style=padding-top: 35px>

A) chlorobenzene
B) chloroaniline
C) anilinium chloride
D) o-chloroaniline
E) N-chloroaniline
Question
The following reaction sequence will produce: <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which molecule is known as an azo compound?

A) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
An imine is produced when a ketone or aldehyde reacts with:

A) methyl alcohol
B) Zn(Hg), HCl
C) an amine
D) an amide
E) HCN
Question
The product(s) from the reaction sequence below is (are): <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The product(s) from the reaction below are: <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
m-Chlorobromobenzene can be prepared in good yield by the sequence:

A) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which reaction will produce a quaternary ammonium salt?

A) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following amines can be converted to an aryl diazonium salt?

A) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
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Deck 11: Amines and Related Nitrogen Compounds
1
Which compound is the strongest base?

A) CH3NH2
B) CH3CO2H
C) CH3CHO
D) CH3OH
E) C6H5NH2
CH3NH2
2
The mechanism by which acylation of an amine with an acid chloride takes place is:

A) nucleophilic acyl substitution
B) electrophilic aromatic substitution
C) nucleophilic addition
D) electrophilic addition
E) nucleophilic aromatic substitution
nucleophilic acyl substitution
3
Which of the following compounds is a tertiary amine?

A) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following compounds is a tertiary amine?</strong> A)   B)   C)   D)   E)
4
The structure below can be named in the following manner: <strong>The structure below can be named in the following manner:  </strong> A) 2-nitrocyclohexanamine B) m-nitroaniline C) o-nitroaniline D) 2-nitrobenzylamine E) 1,2-diaminobenzene

A) 2-nitrocyclohexanamine
B) m-nitroaniline
C) o-nitroaniline
D) 2-nitrobenzylamine
E) 1,2-diaminobenzene
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5
Which of the following are tertiary amines? <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2 <strong>Which of the following are tertiary amines?          </strong> A) 1 and 3 B) only 5 C) 1, 2, 3, and 4 D) 2 and 4 E) 1 and 2

A) 1 and 3
B) only 5
C) 1, 2, 3, and 4
D) 2 and 4
E) 1 and 2
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6
Which of the following amines is the most basic?

A) methylamine
B) dimethylamine
C) ammonia
D) aniline
E) N-methylaniline
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7
What is the mechanism for the intramolecular alkylation shown below?
<strong>What is the mechanism for the intramolecular alkylation shown below?  </strong> A) S<sub>N</sub>2 B) S<sub>N</sub>1 C) nucleophilic acyl substitution D) nucleophilic addition E) electrophilic addition

A) SN2
B) SN1
C) nucleophilic acyl substitution
D) nucleophilic addition
E) electrophilic addition
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8
C6H5NHCH2CH2CH3 can best be prepared as follows:

A) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)
B) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)
C) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)
D) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)
E) <strong>C<sub>6</sub>H<sub>5</sub>NHCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> can best be prepared as follows:</strong> A)   B)   C)   D)   E)
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9
Which of the following is not an intermediate in the diazotization of aniline using nitrous acid? <strong>Which of the following is not an intermediate in the diazotization of aniline using nitrous acid?  </strong> A) I B) II C) III D) IV E) none of the above

A) I
B) II
C) III
D) IV
E) none of the above
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10
When methylamine (CH3NH2) reacts with methyl bromide (CH3Br) to give dimethylamine, the methylamine:

A) acts as an electrophile
B) acts as a Lewis acid
C) acts as a Bronsted-Lowry acid
D) acts as a Bronsted-Lowry base
E) acts as a nucleophile in an SN2 reaction
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11
The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is

A) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)
B) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)
C) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)
D) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)
E) <strong>The structure that corresponds to N-ethyl-2,3-dimethyl-3-hexanamine is</strong> A)   B)   C)   D)   E)
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12
To separate a mixture of p-toluidine and p-nitrotoluene dissolved in ether,

A) extract the ether solution with aqueous HCl and treat the water layer with aqueous NaOH.
B) extract the ether solution with aqueous NaOH and treat the water layer with aqueous HCl.
C) extract the ether solution with water and treat the water layer with aqueous NaOH.
D) extract the ether layer with aqueous HCl and treat the ether layer with aqueous NaOH.
E) extract the ether solution with aqueous HCl and treat the ether layer with aqueous HCl.
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13
Tert-butylamine is classified as a(n) amine.

A) 1°
B) 2°
C) 3°
D) quaternary salt
E) aromatic
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14
The alkylation of an amine with an alkyl halide takes place by the following mechanism:

A) SN1
B) SN2
C) electrophilic addition
D) E1
E) E2
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15
The order of decreasing pKas of the corresponding ammonium ions of the following is: <strong>The order of decreasing pK<sub>a</sub>s of the corresponding ammonium ions of the following is:  </strong> A) 1 > 2 > 3 > 4 B) 3 > 4 > 2 > 1 C) 4 > 3 > 2 > 1 D) 2 > 1 > 3 > 4 E) 4 > 3 > 1 > 2

A) 1 > 2 > 3 > 4
B) 3 > 4 > 2 > 1
C) 4 > 3 > 2 > 1
D) 2 > 1 > 3 > 4
E) 4 > 3 > 1 > 2
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16
The order of increasing basicity of the following is: <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2
<strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2 <strong>The order of increasing basicity of the following is:        </strong> A) 1 < 2 < 3 < 4 B) 2 < 3 < 1 < 4 C) 4 < 3 < 2 < 1 D) 4 < 3 < 1 < 2 E) 4 < 1 < 3 < 2

A) 1 < 2 < 3 < 4
B) 2 < 3 < 1 < 4
C) 4 < 3 < 2 < 1
D) 4 < 3 < 1 < 2
E) 4 < 1 < 3 < 2
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17
The order of decreasing acidity of the following is: <strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1
<strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1
<strong>The order of decreasing acidity of the following is:        </strong> A) 1 > 2 > 3 B) 3 > 1 > 2 C) 2 > 1 > 3 D) 3 > 2 > 1 E) 2 > 3 > 1

A) 1 > 2 > 3
B) 3 > 1 > 2
C) 2 > 1 > 3
D) 3 > 2 > 1
E) 2 > 3 > 1
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18
What structure represents a cationic intermediate in the electrophilic aromatic bromination of aniline? <strong>What structure represents a cationic intermediate in the electrophilic aromatic bromination of aniline?  </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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19
Which of the following molecules has the highest boiling point?

A) ethylamine
B) propane
C) ethyl alcohol
D) dimethyl ether
E) acetaldehyde
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20
Which of the following statements is false:

A) Aliphatic 3o amines with three different groups on nitrogen can be resolved.
B) Primary and secondary aliphatic amines can be hydrogen bond donors.
C) Aliphatic amines can be hydrogen bond acceptors.
D) The non-bonded lone pair in an aliphatic amine is more basic than the non-bonded lone pairs in ethers.
E) The nitrogen in aliphatic amines is sp3-hybridized.
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21
What type of products are formed by diazo coupling reactions?

A) meso compounds
B) azo compounds
C) diazonium salts
D) quaternary ammonium salts
E) racemic mixtures
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22
Aniline <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)   is best prepared via:

A) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)
B) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)
C) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)
D) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)
E) <strong>Aniline    is best prepared via:</strong> A)   B)   C)   D)   E)
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23
What reacts with benzenediazonium chloride to produce benzonitrile?

A) HONO
B) Li, NH3
C) NaBH3CN
D) KCN, Cu2CN2
E) LiAlH4, ether
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24
What is the name of the product formed by reacting CuCl and HCl with benzenediazonium chloride?

A) bromobenzene
B) chlorobenzene
C) o-chloroaniline
D) m-chloroaniline
E) p-chloroaniline
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25
The reaction of a 2o amine with nitrous acid gives:

A) a quaternary ammonium salt
B) a nitrosamine
C) A diazonium salt
D) an azo dye
E) a nitro compound
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26
Reacting aniline, C6H5NH2, with a primary alkyl halide will produce a(n):

A) 1° amine
B) 2° amine
C) 3° amine
D) amide
E) imine
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27
The product(s) of <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)   are:

A) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)
B) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)
C) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)
D) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)
E) <strong>The product(s) of    are:</strong> A)   B)   C)   D)   E)
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28
m-Dichlorobenzene can be prepared in good yield by the sequence:

A) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
B) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
C) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
D) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
E) <strong>m-Dichlorobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
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29
What is the final product for the following sequence of reactions?
<strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)

A) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)
B) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)
C) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)
D) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)
E) <strong>What is the final product for the following sequence of reactions?  </strong> A)   B)   C)   D)   E)
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30
What is the stereochemical relationship of the products formed by reacting racemic lactic acid with (S)-1-phenylethylamine?

A) enantiomers
B) meso compounds
C) racemic mixture
D) diastereomers
E) geometric isomers
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31
The amines that can be acylated by acetic anhydride are <strong>The amines that can be acylated by acetic anhydride are  </strong> A) only 4 B) 1, 2, 3, and 4 C) 1 and 3 D) 2 and 4 E) only 2

A) only 4
B) 1, 2, 3, and 4
C) 1 and 3
D) 2 and 4
E) only 2
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32
What is the name of the product of the following reaction? <strong>What is the name of the product of the following reaction?  </strong> A) chlorobenzene B) chloroaniline C) anilinium chloride D) o-chloroaniline E) N-chloroaniline

A) chlorobenzene
B) chloroaniline
C) anilinium chloride
D) o-chloroaniline
E) N-chloroaniline
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33
The following reaction sequence will produce: <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)

A) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)
B) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)
C) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)
D) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)
E) <strong>The following reaction sequence will produce:   </strong> A)   B)   C)   D)   E)
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34
Which molecule is known as an azo compound?

A) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)
B) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)
C) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)
D) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)
E) <strong>Which molecule is known as an azo compound?</strong> A)   B)   C)   D)   E)
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35
An imine is produced when a ketone or aldehyde reacts with:

A) methyl alcohol
B) Zn(Hg), HCl
C) an amine
D) an amide
E) HCN
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36
The product(s) from the reaction sequence below is (are): <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)

A) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)
B) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)
C) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)
D) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)
E) <strong>The product(s) from the reaction sequence below is (are):  </strong> A)   B)   C)   D)   E)
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37
The product(s) from the reaction below are: <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)

A) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)
B) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)
C) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)
D) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)
E) <strong>The product(s) from the reaction below are:    </strong> A)   B)   C)   D)   E)
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38
m-Chlorobromobenzene can be prepared in good yield by the sequence:

A) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
B) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
C) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
D) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
E) <strong>m-Chlorobromobenzene can be prepared in good yield by the sequence:</strong> A)   B)   C)   D)   E)
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39
Which reaction will produce a quaternary ammonium salt?

A) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)
B) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)
C) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)
D) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)
E) <strong>Which reaction will produce a quaternary ammonium salt?</strong> A)   B)   C)   D)   E)
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40
Which of the following amines can be converted to an aryl diazonium salt?

A) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the following amines can be converted to an aryl diazonium salt?</strong> A)   B)   C)   D)   E)
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