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Why are alkylamines more basic than arylamines?


A) The lone pair electrons are localized in alkylamines and delocalized in arylamines.
B) The lone pair electrons are delocalized in alkylamines and localized in arylamines.
C) The lone pair electrons are less readily available in alkylamines.
D) The lone pair electrons are more readily available in arylamines.

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

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In the preparation of primary amines,how can direct nucleophilic substitution between NH3 and alkyl halide be made more practical than reacting NH3 and the alkyl halide in a 1:1 ratio?


A) Use a large excess of NH3.
B) Use a large excess of alkyl halide.
C) Use a limited amount of NH3.
D) Make the alkyl halide sterically hindered.

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

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?   A) 3-methyl-1-hexanamine B) 4-methyl-1-hexylamine C) 4-methyl-1-hexanamine D) 3-methyl-6-hexylamine


A) 3-methyl-1-hexanamine
B) 4-methyl-1-hexylamine
C) 4-methyl-1-hexanamine
D) 3-methyl-6-hexylamine

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

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Rank the following compounds in order of increasing basicity,putting the least basic first. Rank the following compounds in order of increasing basicity,putting the least basic first.   A) II < III < IV < I B) I < II < III < IV C) IV < III < II < I D) II < I < III < IV


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

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

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What is the common name of the following compound? What is the common name of the following compound?   A) diisopropylamine B) dipropylamine C) diisopropanamine D) dibutylamine


A) diisopropylamine
B) dipropylamine
C) diisopropanamine
D) dibutylamine

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

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A

What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?   A) N-ethyl-N-methylpentylamine B) N-ethyl-N-methyl-1-pentanamine C) N-methyl-3-octanamine D) N-ethyl-2-heptanamine


A) N-ethyl-N-methylpentylamine
B) N-ethyl-N-methyl-1-pentanamine
C) N-methyl-3-octanamine
D) N-ethyl-2-heptanamine

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

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Why is pyrrole much less basic than pyridine?


A) The lone pair of electrons in pyrrole is located on an sp2 orbital.
B) The lone pair of electrons in pyrrole is part of the aromatic p system.
C) The lone pair of electrons in pyrrole is not part of the aromatic p system.
D) The pKa of the conjugate acid of pyrrole is much greater than the conjugate acid of pyridine.

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

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What is the common name of the following compound? What is the common name of the following compound?   A) isopropylamine B) sec-butylamine C) isobutylamine D) tert-butylamine


A) isopropylamine
B) sec-butylamine
C) isobutylamine
D) tert-butylamine

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

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What is the major organic product obtained in the following reaction? What is the major organic product obtained in the following reaction?   A) I B) II C) III D) IV


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

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

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Rank the following compounds in increasing order of basicity,putting the least basic first. Rank the following compounds in increasing order of basicity,putting the least basic first.   A) II < I < IV < III B) I < III < II < IV C) IV < II < III < I D) I < II < III < IV


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

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

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Predict the major organic product of the following reaction. Predict the major organic product of the following reaction.   A) I B) II C) III D) IV


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

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

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Predict the major organic product of the following reaction. Predict the major organic product of the following reaction.   A) I B) II C) III D) IV


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

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

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What is the common name of the following compound? What is the common name of the following compound?   A) dimethylisobutylamine B) butyldimethylamine C) N,N-dimethylbutanamine D) sec-butyldimethylamine


A) dimethylisobutylamine
B) butyldimethylamine
C) N,N-dimethylbutanamine
D) sec-butyldimethylamine

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

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D

The mass spectrum of an amine shows a parent peak with an odd mass for the molecular ion.What does this tell you about the amine?


A) The amine is a primary amine.
B) The amine is a secondary amine.
C) The amine contains an even number of N atoms.
D) The amine contains an odd number of N atoms.

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

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What is the correct assignment of the names of the following aromatic amines? What is the correct assignment of the names of the following aromatic amines?   A) I = pyrrolidine; II = pyrimidine; III = aniline B) I = pyrrole; II = pyrimidine; III = anisole C) I = pyrrolidine; II = pyridine; III =aniline D) I = pyrrole; II = pyridine; III = aniline


A) I = pyrrolidine; II = pyrimidine; III = aniline
B) I = pyrrole; II = pyrimidine; III = anisole
C) I = pyrrolidine; II = pyridine; III =aniline
D) I = pyrrole; II = pyridine; III = aniline

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

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What is the major organic product obtained in the following reaction? What is the major organic product obtained in the following reaction?   A) I B) II C) III D) IV


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

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

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B

Which of the following amines are classified as secondary (2°) amines? Which of the following amines are classified as secondary (2°) amines?   A) I B) II C) III D) I and II


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

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

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Select the reagent(s) required for the following transformation. Select the reagent(s) required for the following transformation.   A) (1) NaNO<sub>2</sub>,HCl; (2) H<sub>2</sub> B) (1) NaNO<sub>2</sub>,HCl; (2) H<sub>2</sub>O C) (1) NaNO<sub>2</sub>,HCl; (2) H<sub>3</sub>PO<sub>4</sub> D) (1) NaNO<sub>2</sub>,HCl; (2) H<sub>3</sub>PO<sub>2</sub>


A) (1) NaNO2,HCl; (2) H2
B) (1) NaNO2,HCl; (2) H2O
C) (1) NaNO2,HCl; (2) H3PO4
D) (1) NaNO2,HCl; (2) H3PO2

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

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What is the common name of the following compound? What is the common name of the following compound?   A) isopropylamine B) 2-methyl-2-propanamine C) tert-butylamine D) isobutylamine


A) isopropylamine
B) 2-methyl-2-propanamine
C) tert-butylamine
D) isobutylamine

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

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Consider the following multistep synthesis. Consider the following multistep synthesis.   What is the structure of intermediate B?   A) I B) II C) III D) IV What is the structure of intermediate B? Consider the following multistep synthesis.   What is the structure of intermediate B?   A) I B) II C) III D) IV


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

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

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