Deck 4: Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis

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Question
An IUPAC name for <strong>An IUPAC name for   is:</strong> A) 3-Isobutyl-2,4-dimethylhexane B) 3-sec-Butyl-2,5-dimethylhexane C) 4-sec-Butyl-2,5-dimethylhexane D) 4-Isopropyl-2,5-dimethylheptane E) 4-Isopropyl-3,6-dimethylheptane <div style=padding-top: 35px> is:

A) 3-Isobutyl-2,4-dimethylhexane
B) 3-sec-Butyl-2,5-dimethylhexane
C) 4-sec-Butyl-2,5-dimethylhexane
D) 4-Isopropyl-2,5-dimethylheptane
E) 4-Isopropyl-3,6-dimethylheptane
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Question
Which of these is the common name for the 1,1-dimethylpropyl group?

A) tert-Butyl
B) tert-Pentyl
C) Isopentyl
D) Neopentyl
E) sec-Pentyl
Question
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 2,5-Dimethyl-3-propylheptane B) 3,6-Dimethyl-5-propylheptane C) 6-Methyl-4-(1-methylethyl)octane D) 2-Methyl-3-(2-methylbutyl)hexane E) 3-Methyl-5-(1-methylethyl)octane <div style=padding-top: 35px>

A) 2,5-Dimethyl-3-propylheptane
B) 3,6-Dimethyl-5-propylheptane
C) 6-Methyl-4-(1-methylethyl)octane
D) 2-Methyl-3-(2-methylbutyl)hexane
E) 3-Methyl-5-(1-methylethyl)octane
Question
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 3-Hydroxymethylheptane B) 3-Hydroxymethylhexane C) 3-Methyloxyheptane D) 2-Ethyl-1-hexanol E) 2-Ethyl-1-heptanol <div style=padding-top: 35px>

A) 3-Hydroxymethylheptane
B) 3-Hydroxymethylhexane
C) 3-Methyloxyheptane
D) 2-Ethyl-1-hexanol
E) 2-Ethyl-1-heptanol
Question
How many compounds with the formula C7H16 (heptanes)contain a single 3° carbon atom?

A) 2
B) 3
C) 4
D) 5
E) 6
Question
What is the simplest alkane,i.e. ,the one with the smallest molecular weight,which possesses primary,secondary and tertiary carbon atoms?

A) 2-Methylpropane
B) 2-Methylbutane
C) 2-Methylpentane
D) 3-Methylpentane
E) 2,2-Dimethylbutane
Question
Which of the following pairs of compounds represent pairs of constitutional isomers?

A) 2-Methylbutane and pentane
B) 2-Chlorohexane and 3-chlorohexane
C) sec-Butyl bromide and tert-butyl bromide
D) Propyl chloride and isopropyl chloride
E) All of the above
Question
The neopentyl group has the alternative name:

A) 1,1-Dimethylpropyl
B) 1,2-Dimethylpropyl
C) 2,2-Dimethylpropyl
D) 1-Methylbutyl
E) 2-Methylbutyl
Question
What is the common name for this compound? <strong>What is the common name for this compound?  </strong> A) Isobutyl bromide B) tert-Butyl bromide C) Butyl bromide D) sec-Butyl bromide E) Bromo-sec-butane <div style=padding-top: 35px>

A) Isobutyl bromide
B) tert-Butyl bromide
C) Butyl bromide
D) sec-Butyl bromide
E) Bromo-sec-butane
Question
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 5-Ethyl-3-methylhexanol B) 5-Ethyl-3-methyl-1-hexanol C) 2-Ethyl-4-methyl-6-hexanol D) 3,5-Dimethyl-7-heptanol E) 3,5-Dimethyl-1-heptanol <div style=padding-top: 35px>

A) 5-Ethyl-3-methylhexanol
B) 5-Ethyl-3-methyl-1-hexanol
C) 2-Ethyl-4-methyl-6-hexanol
D) 3,5-Dimethyl-7-heptanol
E) 3,5-Dimethyl-1-heptanol
Question
How many alkanes of formula C7H16 possess a quaternary carbon atom?

A) 1
B) 2
C) 3
D) 4
E) 5
Question
An IUPAC name for the group <strong>An IUPAC name for the group   is:</strong> A) Isopentyl B) Isoamyl C) sec-Butylmethyl D) 2-Methylbutyl E) 2-Ethylpropyl <div style=padding-top: 35px> is:

A) Isopentyl
B) Isoamyl
C) sec-Butylmethyl
D) 2-Methylbutyl
E) 2-Ethylpropyl
Question
The correct IUPAC name for <strong>The correct IUPAC name for   is:</strong> A) 2-Bromo-4-chloro-4-isopropylpentane B) 4-Bromo-2-chloro-2-isopropylpentane C) 5-Bromo-3-chloro-2,3-dimethylhexane D) 2-Bromo-4-chloro-4,5-dimethylhexane E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane <div style=padding-top: 35px> is:

A) 2-Bromo-4-chloro-4-isopropylpentane
B) 4-Bromo-2-chloro-2-isopropylpentane
C) 5-Bromo-3-chloro-2,3-dimethylhexane
D) 2-Bromo-4-chloro-4,5-dimethylhexane
E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane
Question
How many constitutional isomers are possible for the formula C6H14?

A) 2
B) 3
C) 4
D) 5
E) 6
Question
An IUPAC name for <strong>An IUPAC name for   is:</strong> A) 5-Methyl-4-(1-methylpropyl)hexane B) 2-Methyl-3-(1-methylpropyl)hexane C) 2-Methyl-3-(2-methylpropyl)hexane D) 3-Methyl-4-(1-methylethyl)heptane E) 5-Methyl-4-(1-methylethyl)heptane <div style=padding-top: 35px> is:

A) 5-Methyl-4-(1-methylpropyl)hexane
B) 2-Methyl-3-(1-methylpropyl)hexane
C) 2-Methyl-3-(2-methylpropyl)hexane
D) 3-Methyl-4-(1-methylethyl)heptane
E) 5-Methyl-4-(1-methylethyl)heptane
Question
An IUPAC name for the following compound is: <strong>An IUPAC name for the following compound is:  </strong> A) 4-Isobutyl-3,4-dimethylheptane B) 4-sec-Butyl-2,4-dimethylheptane C) 2,4,5-Trimethyl-4-propylheptane D) 3,4,6-Trimethyl-4-propylheptane E) 4-Isobutyl-4,5-dimethylheptane <div style=padding-top: 35px>

A) 4-Isobutyl-3,4-dimethylheptane
B) 4-sec-Butyl-2,4-dimethylheptane
C) 2,4,5-Trimethyl-4-propylheptane
D) 3,4,6-Trimethyl-4-propylheptane
E) 4-Isobutyl-4,5-dimethylheptane
Question
What is a correct name for the following compound? <strong>What is a correct name for the following compound?  </strong> A) 3-Isobutyl-2-methylheptane B) 3-sec-Butyl-2-methyloctane C) 5-Isobutyl-6-methylheptane D) 2-Ethyl-3-isopropyloctane E) 4-Isopropyl-3-methylnonane <div style=padding-top: 35px>

A) 3-Isobutyl-2-methylheptane
B) 3-sec-Butyl-2-methyloctane
C) 5-Isobutyl-6-methylheptane
D) 2-Ethyl-3-isopropyloctane
E) 4-Isopropyl-3-methylnonane
Question
Isopentyl is the common name for which alkyl group?

A)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The IUPAC name for <strong>The IUPAC name for   is:</strong> A) 6-Ethyl-3,4-dimethylheptane B) 2-Ethyl-4,5-dimethylheptane C) 3,4,6-Trimethyloctane D) 3,5,6-Trimethyloctane E) 2-(1-Methylpropyl)-4-methylhexane <div style=padding-top: 35px> is:

A) 6-Ethyl-3,4-dimethylheptane
B) 2-Ethyl-4,5-dimethylheptane
C) 3,4,6-Trimethyloctane
D) 3,5,6-Trimethyloctane
E) 2-(1-Methylpropyl)-4-methylhexane
Question
Neglecting stereochemistry,which of these common group names is ambiguous,i.e. ,does not refer to one specific group?

A) Butyl
B) sec-Butyl
C) tert-Pentyl
D) Neopentyl
E) sec-Pentyl
Question
Which is the correct name for the compound shown below? <strong>Which is the correct name for the compound shown below?  </strong> A) Bicyclo[2.2.0]hexane B) Bicyclo[2.2.0]butane C) Bicyclo[2.2.2]hexane D) Bicyclo[2.2.1]hexane E) Disquarane <div style=padding-top: 35px>

A) Bicyclo[2.2.0]hexane
B) Bicyclo[2.2.0]butane
C) Bicyclo[2.2.2]hexane
D) Bicyclo[2.2.1]hexane
E) Disquarane
Question
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 3-chloro-8-methylbicyclo[4.3.0]nonane B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane D) 3-Methyl-7-chlorobicyclo[4.3.1]decane E) 3-chloro-8-methyl[4.3.0]bicyclononane <div style=padding-top: 35px>

A) 3-chloro-8-methylbicyclo[4.3.0]nonane
B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane
C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane
D) 3-Methyl-7-chlorobicyclo[4.3.1]decane
E) 3-chloro-8-methyl[4.3.0]bicyclononane
Question
The most stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The most stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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 least stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The least stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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 compound is a bicycloheptane? <strong>Which compound is a bicycloheptane?  </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 most stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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 correct name of the following compound? <strong>What is the correct name of the following compound?  </strong> A) 1-Chlorobicyclo[4.1.1]octane B) 2-Chlorobicyclo[4.1.0]octane C) 2-Chlorobicyclo[4.1.1]octane D) 2-Chlorobicyclo[4.1.1]heptane E) 5-Chlorobicyclo[4.1.1]octane <div style=padding-top: 35px>

A) 1-Chlorobicyclo[4.1.1]octane
B) 2-Chlorobicyclo[4.1.0]octane
C) 2-Chlorobicyclo[4.1.1]octane
D) 2-Chlorobicyclo[4.1.1]heptane
E) 5-Chlorobicyclo[4.1.1]octane
Question
<strong>  Which of the above is bicyclo[4.3.0]nonane?</strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>
Which of the above is bicyclo[4.3.0]nonane?

A) I
B) II
C) III
D) IV
E) V
Question
What is the name of this compound? <strong>What is the name of this compound?  </strong> A) Bicyclo[2.2.2]octane B) Bicyclo[3.2.1]octane C) Bicyclo[4.1.1]octane D) Bicyclo[4.2.0]octane E) Bicyclo[3.3.0]octane <div style=padding-top: 35px>

A) Bicyclo[2.2.2]octane
B) Bicyclo[3.2.1]octane
C) Bicyclo[4.1.1]octane
D) Bicyclo[4.2.0]octane
E) Bicyclo[3.3.0]octane
Question
Which of the following is bicyclo[3.2.2]nonane? <strong>Which of the following is bicyclo[3.2.2]nonane?  </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 is a correct name which corresponds to the common name tert-pentyl alcohol?

A) 2,2-Dimethyl-1-propanol
B) 2-Ethyl-2-propanol
C) 2-Methyl-2-butanol
D) 3-Methyl-1-butanol
E) Methyl tert-butanol
Question
The correct IUPAC name for the following compound is: <strong>The correct IUPAC name for the following compound is:  </strong> A) 1-Hydroxy-3-sec-butylcyclopentane B) 3-sec-Butyl-1-cyclopentanol C) 1-sec-Butyl-3-cyclopentanol D) 4-sec-Butyl-1-cyclopentanol E) 3-Isobutyl-1-cyclopentanol <div style=padding-top: 35px>

A) 1-Hydroxy-3-sec-butylcyclopentane
B) 3-sec-Butyl-1-cyclopentanol
C) 1-sec-Butyl-3-cyclopentanol
D) 4-sec-Butyl-1-cyclopentanol
E) 3-Isobutyl-1-cyclopentanol
Question
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane <div style=padding-top: 35px>

A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane
B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane
C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane
D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane
E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane
Question
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 5-Ethyl-3-fluorohexanol B) 5-Ethyl-3-fluoro-1-hexanol C) 2-Ethyl-4-fluoro-6-hexanol D) 3-fluoro-5-methyl-7-heptanol E) 3-fluoro-5-methyl-1-heptanol <div style=padding-top: 35px>

A) 5-Ethyl-3-fluorohexanol
B) 5-Ethyl-3-fluoro-1-hexanol
C) 2-Ethyl-4-fluoro-6-hexanol
D) 3-fluoro-5-methyl-7-heptanol
E) 3-fluoro-5-methyl-1-heptanol
Question
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 4-propyl-5-chloro-3-heptanol B) 4-propyl-3-chloro-5-heptanol C) 4-(1-chloropropyl)-3-heptanol D) 5-chloro-4-propyl-3-heptanol E) 3-hydroxy-4-propyl-5-chloroheptane <div style=padding-top: 35px>

A) 4-propyl-5-chloro-3-heptanol
B) 4-propyl-3-chloro-5-heptanol
C) 4-(1-chloropropyl)-3-heptanol
D) 5-chloro-4-propyl-3-heptanol
E) 3-hydroxy-4-propyl-5-chloroheptane
Question
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 2-Methylbicyclo[4.3.0]nonane B) 1-Methylbicyclo[4.3.1]nonane C) 7-Methylbicyclo[4.3.0]nonane D) 2-Methylbicyclo[4.3.1]nonane E) 1-Methylbicyclo[4.3.0]nonane <div style=padding-top: 35px>

A) 2-Methylbicyclo[4.3.0]nonane
B) 1-Methylbicyclo[4.3.1]nonane
C) 7-Methylbicyclo[4.3.0]nonane
D) 2-Methylbicyclo[4.3.1]nonane
E) 1-Methylbicyclo[4.3.0]nonane
Question
<strong>  Which of the above is bicyclo[3.3.1]nonane?</strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>
Which of the above is bicyclo[3.3.1]nonane?

A) I
B) II
C) III
D) IV
E) V
Question
Which of the following structures represents bicyclo[3.2.1]octane? <strong>Which of the following structures represents bicyclo[3.2.1]octane?  </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
<strong>  Which of the above is bicyclo[5.2.0]nonane?</strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>
Which of the above is bicyclo[5.2.0]nonane?

A) I
B) II
C) III
D) IV
E) V
Question
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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
Select the systematic name for <strong>Select the systematic name for  </strong> A) cis-1,3-Dichlorocyclopentane B) trans-1,4-Dichlorocyclopentane C) cis-1,2-Dichlorocyclopentane D) trans-1,3-Dichlorocyclopentane E) 1,1-Dichlorocyclopentane <div style=padding-top: 35px>

A) cis-1,3-Dichlorocyclopentane
B) trans-1,4-Dichlorocyclopentane
C) cis-1,2-Dichlorocyclopentane
D) trans-1,3-Dichlorocyclopentane
E) 1,1-Dichlorocyclopentane
Question
Consider the graph below,which is a plot of the relative energies of the various conformations of hexane,viewed through the C-2-C-3 bond.The conformations corresponding to the 60o and 300o are: <strong>Consider the graph below,which is a plot of the relative energies of the various conformations of hexane,viewed through the C-2-C-3 bond.The conformations corresponding to the 60<sup>o</sup> and 300<sup>o</sup> are:  </strong> A) Eclipsed B) Staggered and gauche C) Staggered and anti D) More stable than the conformation at 180<sup>o</sup> E) None of the above <div style=padding-top: 35px>

A) Eclipsed
B) Staggered and gauche
C) Staggered and anti
D) More stable than the conformation at 180o
E) None of the above
Question
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): <strong>The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back):  </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 conformation(s)of 1,2-dibromoethane does not illustrate one or more gauche interactions? <strong>Which conformation(s)of 1,2-dibromoethane does not illustrate one or more gauche interactions?  </strong> A) I and II only B) II,III,and V only C) I,III,and IV only D) All but one above E) All the above <div style=padding-top: 35px>

A) I and II only
B) II,III,and V only
C) I,III,and IV only
D) All but one above
E) All the above
Question
The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): <strong>The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back):  </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 the most stable conformation of cyclohexane?

A) Chair
B) Twist
C) Boat
D) One-half chair
E) Staggered
Question
Consider the graph below,which is a plot of the relative energies of the various conformations of 2,3-dimethylbutane,viewed through the C-2-C-3 bond.The conformations corresponding to the 120o and 240o are: <strong>Consider the graph below,which is a plot of the relative energies of the various conformations of 2,3-dimethylbutane,viewed through the C-2-C-3 bond.The conformations corresponding to the 120<sup>o</sup> and 240<sup>o</sup> are:  </strong> A) Eclipsed,more stable than the conformation at 0<sup>o</sup> B) Eclipsed,more stable than the conformation at 180<sup>o</sup> C) Staggered,more stable than the conformation at 0<sup>o</sup> D) Staggered,less stable than the conformation at 180<sup>o</sup> E) Two of the above are true <div style=padding-top: 35px>

A) Eclipsed,more stable than the conformation at 0o
B) Eclipsed,more stable than the conformation at 180o
C) Staggered,more stable than the conformation at 0o
D) Staggered,less stable than the conformation at 180o
E) Two of the above are true
Question
The most stable conformation for 1,2-ethanediol (ethylene glycol)is shown below.It is the most stable conformation because: <strong>The most stable conformation for 1,2-ethanediol (ethylene glycol)is shown below.It is the most stable conformation because:  </strong> A) this corresponds to an anti conformation. B) in general,gauche conformations possess the minimum energy. C) it is stabilized by intramolecular hydrogen bonding. D) it is a staggered conformation. E) it has the highest energy of all the possibilities. <div style=padding-top: 35px>

A) this corresponds to an anti conformation.
B) in general,gauche conformations possess the minimum energy.
C) it is stabilized by intramolecular hydrogen bonding.
D) it is a staggered conformation.
E) it has the highest energy of all the possibilities.
Question
The most stable conformation of butane is: <strong>The most stable conformation of butane 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
Give the IUPAC name for <strong>Give the IUPAC name for  </strong> A) 3-Methyl-4-hexyne B) 4-Methyl-2-hexyne C) 2-Ethyl-3-pentyne D) 4-Ethyl-2-pentyne E) 3-Methyl-2-hexyne <div style=padding-top: 35px>

A) 3-Methyl-4-hexyne
B) 4-Methyl-2-hexyne
C) 2-Ethyl-3-pentyne
D) 4-Ethyl-2-pentyne
E) 3-Methyl-2-hexyne
Question
The least stable conformation of butane is: <strong>The least stable conformation of butane 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 most stable conformation of 1,2-dibromoethane is: <strong>The most stable conformation of 1,2-dibromoethane 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 graph below is a plot of the relative energies of the various conformations of: <strong>The graph below is a plot of the relative energies of the various conformations of:  </strong> A) 2-chloropropane B) 1,3-dichloropropane C) 2-methylpropane D) Butane (C1-C2 rotation) E) Butane (C2-C3 rotation) <div style=padding-top: 35px>

A) 2-chloropropane
B) 1,3-dichloropropane
C) 2-methylpropane
D) Butane (C1-C2 rotation)
E) Butane (C2-C3 rotation)
Question
The IUPAC name for diisobutylacetylene is

A) 2,7-Dimethyl-4-octene
B) 2,7-Dimethyl-4-octyne
C) 3,6-Dimethyl-4-octyne
D) 2,5-Diethyl-3-hexyne
E) 2,2,5,5-Tetramethyl-3-hexyne
Question
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 3,6,7-trimethyl-4-bromo-1-octene B) 4-bromo-3-methyl-6-isopropyl-1-heptene C) 4-bromo-3,6,7-trimethyl-1-octene D) 4-bromo-6-isopropyl-3-methyl-1-heptene E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene <div style=padding-top: 35px>

A) 3,6,7-trimethyl-4-bromo-1-octene
B) 4-bromo-3-methyl-6-isopropyl-1-heptene
C) 4-bromo-3,6,7-trimethyl-1-octene
D) 4-bromo-6-isopropyl-3-methyl-1-heptene
E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene
Question
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) trans-3-Hydroxymethyl-2-heptene B) trans-2-(1-methylethyl)-4-hexen-1-ol C) trans-5-(1-methylethyl)-2-hexen-6-ol D) cis-5-isopropyl-2,6-hexenol E) cis-2-(1-methylethyl)-4-hepten-1-ol <div style=padding-top: 35px>

A) trans-3-Hydroxymethyl-2-heptene
B) trans-2-(1-methylethyl)-4-hexen-1-ol
C) trans-5-(1-methylethyl)-2-hexen-6-ol
D) cis-5-isopropyl-2,6-hexenol
E) cis-2-(1-methylethyl)-4-hepten-1-ol
Question
Which cycloalkane has the greatest ring strain?

A) Cyclopropane
B) Cyclobutane
C) Cyclopentane
D) Cyclohexane
E) Cycloheptane
Question
The graph below is a plot of the relative energies of the various conformations of: <strong>The graph below is a plot of the relative energies of the various conformations of:  </strong> A) Ethane B) Propane C) Chloroethane D) 1-Chloropropane (C1-C2 rotation) E) Butane (C1-C2 rotation) <div style=padding-top: 35px>

A) Ethane
B) Propane
C) Chloroethane
D) 1-Chloropropane (C1-C2 rotation)
E) Butane (C1-C2 rotation)
Question
The least stable conformation of cyclohexane is the:

A) boat.
B) twist boat.
C) chair.
D) half-chair.
E) twist chair.
Question
The least stable conformation of butane is: <strong>The least stable conformation of butane 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 conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane? <strong>Which conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane?  </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 most stable conformation of cis-1-tert-butyl-2-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
Question
The most stable conformation of trans-1-tert-butyl-2-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the molecule is in the half chair conformation.
Question
<strong>  trans-1,2-Dibromocyclohexane is represented by structure(s):</strong> A) I B) II C) III D) II and III E) I and II <div style=padding-top: 35px>
trans-1,2-Dibromocyclohexane is represented by structure(s):

A) I
B) II
C) III
D) II and III
E) I and II
Question
How many moles of hydrogen (H2)will react with 3-cyclobutylpropan-1-ol?

A) 1
2
B) 2
C) 3
D) 4
E) None of the above
Question
What structure represents the most stable conformation of cis-1,3-dimethylcyclohexane? <strong>What structure represents the most stable conformation of cis-1,3-dimethylcyclohexane?  </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
Select the structure for cis-3-methyl-6-vinylcyclohexene. <strong>Select the structure for cis-3-methyl-6-vinylcyclohexene.  </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
Catalytic hydrogenation of which of the following will yield 2-methylpentane?

A) 2-methyl-1-pentene
2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above
Question
In the most stable conformation of cis-1,4-dimethylcyclohexane,the methyl groups are:

A) one axial,one equatorial.
B) both axial.
C) both equatorial.
D) alternating between being both axial and both equatorial.
E) None of the above
Question
Which of these C10H18 isomers is predicted to be the most stable? <strong>Which of these C<sub>10</sub>H<sub>18</sub> isomers is predicted to be the most stable?  </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 will have the same energy after undergoing ring flip? <strong>Which of the following will have the same energy after undergoing ring flip?  </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 twist boat conformation is the preferred conformation for this compound.

A) cis-1,4-Di-tert-butylcyclohexane
B) trans-1,4-Di-tert-butylcyclohexane
C) cis-1,3-Di-tert-butylcyclohexane
D) trans-1,2-Di-tert-butylcyclohexane
E) None of these
Question
How many moles of hydrogen (H2)will react with (trans,trans)-hepta-3,5-dien-1-yne?

A) 1
2
B) 2
C) 3
D) 4
E) 5
Question
The most stable conformation of trans-1-tert-butyl-3-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
Question
cis-1,3-Dibromocyclohexane is represented by structure(s): <strong>cis-1,3-Dibromocyclohexane is represented by structure(s):  </strong> A) I B) II C) III D) II and III E) I and II <div style=padding-top: 35px>

A) I
B) II
C) III
D) II and III
E) I and II
Question
Which of the following can be described as trans isomers? <strong>Which of the following can be described as trans isomers?   </strong> A) I B) II,V C) III,IV D) I,III and IV E) None of the above are trans isomers. <div style=padding-top: 35px>

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are trans isomers.
Question
<strong>  cis-1,2-Dibromocyclohexane is represented by structure(s):</strong> A) I B) II C) III D) II and III E) I and II <div style=padding-top: 35px>
cis-1,2-Dibromocyclohexane is represented by structure(s):

A) I
B) II
C) III
D) II and III
E) I and II
Question
Select the reagents necessary to convert cyclopentene into cyclopentane.

A) H2 and Ni
B) H2O
C) Heat
D) Zn,H3O+
E) Light
Question
Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?

A)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following can be described as cis isomers? <strong>Which of the following can be described as cis isomers?  </strong> A) I B) II,V C) III,IV D) I,III and IV E) None of the above are cis isomers. <div style=padding-top: 35px>

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are cis isomers.
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Deck 4: Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis
1
An IUPAC name for <strong>An IUPAC name for   is:</strong> A) 3-Isobutyl-2,4-dimethylhexane B) 3-sec-Butyl-2,5-dimethylhexane C) 4-sec-Butyl-2,5-dimethylhexane D) 4-Isopropyl-2,5-dimethylheptane E) 4-Isopropyl-3,6-dimethylheptane is:

A) 3-Isobutyl-2,4-dimethylhexane
B) 3-sec-Butyl-2,5-dimethylhexane
C) 4-sec-Butyl-2,5-dimethylhexane
D) 4-Isopropyl-2,5-dimethylheptane
E) 4-Isopropyl-3,6-dimethylheptane
4-Isopropyl-2,5-dimethylheptane
2
Which of these is the common name for the 1,1-dimethylpropyl group?

A) tert-Butyl
B) tert-Pentyl
C) Isopentyl
D) Neopentyl
E) sec-Pentyl
tert-Pentyl
3
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 2,5-Dimethyl-3-propylheptane B) 3,6-Dimethyl-5-propylheptane C) 6-Methyl-4-(1-methylethyl)octane D) 2-Methyl-3-(2-methylbutyl)hexane E) 3-Methyl-5-(1-methylethyl)octane

A) 2,5-Dimethyl-3-propylheptane
B) 3,6-Dimethyl-5-propylheptane
C) 6-Methyl-4-(1-methylethyl)octane
D) 2-Methyl-3-(2-methylbutyl)hexane
E) 3-Methyl-5-(1-methylethyl)octane
3-Methyl-5-(1-methylethyl)octane
4
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 3-Hydroxymethylheptane B) 3-Hydroxymethylhexane C) 3-Methyloxyheptane D) 2-Ethyl-1-hexanol E) 2-Ethyl-1-heptanol

A) 3-Hydroxymethylheptane
B) 3-Hydroxymethylhexane
C) 3-Methyloxyheptane
D) 2-Ethyl-1-hexanol
E) 2-Ethyl-1-heptanol
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5
How many compounds with the formula C7H16 (heptanes)contain a single 3° carbon atom?

A) 2
B) 3
C) 4
D) 5
E) 6
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6
What is the simplest alkane,i.e. ,the one with the smallest molecular weight,which possesses primary,secondary and tertiary carbon atoms?

A) 2-Methylpropane
B) 2-Methylbutane
C) 2-Methylpentane
D) 3-Methylpentane
E) 2,2-Dimethylbutane
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7
Which of the following pairs of compounds represent pairs of constitutional isomers?

A) 2-Methylbutane and pentane
B) 2-Chlorohexane and 3-chlorohexane
C) sec-Butyl bromide and tert-butyl bromide
D) Propyl chloride and isopropyl chloride
E) All of the above
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8
The neopentyl group has the alternative name:

A) 1,1-Dimethylpropyl
B) 1,2-Dimethylpropyl
C) 2,2-Dimethylpropyl
D) 1-Methylbutyl
E) 2-Methylbutyl
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9
What is the common name for this compound? <strong>What is the common name for this compound?  </strong> A) Isobutyl bromide B) tert-Butyl bromide C) Butyl bromide D) sec-Butyl bromide E) Bromo-sec-butane

A) Isobutyl bromide
B) tert-Butyl bromide
C) Butyl bromide
D) sec-Butyl bromide
E) Bromo-sec-butane
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10
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 5-Ethyl-3-methylhexanol B) 5-Ethyl-3-methyl-1-hexanol C) 2-Ethyl-4-methyl-6-hexanol D) 3,5-Dimethyl-7-heptanol E) 3,5-Dimethyl-1-heptanol

A) 5-Ethyl-3-methylhexanol
B) 5-Ethyl-3-methyl-1-hexanol
C) 2-Ethyl-4-methyl-6-hexanol
D) 3,5-Dimethyl-7-heptanol
E) 3,5-Dimethyl-1-heptanol
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11
How many alkanes of formula C7H16 possess a quaternary carbon atom?

A) 1
B) 2
C) 3
D) 4
E) 5
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12
An IUPAC name for the group <strong>An IUPAC name for the group   is:</strong> A) Isopentyl B) Isoamyl C) sec-Butylmethyl D) 2-Methylbutyl E) 2-Ethylpropyl is:

A) Isopentyl
B) Isoamyl
C) sec-Butylmethyl
D) 2-Methylbutyl
E) 2-Ethylpropyl
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13
The correct IUPAC name for <strong>The correct IUPAC name for   is:</strong> A) 2-Bromo-4-chloro-4-isopropylpentane B) 4-Bromo-2-chloro-2-isopropylpentane C) 5-Bromo-3-chloro-2,3-dimethylhexane D) 2-Bromo-4-chloro-4,5-dimethylhexane E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane is:

A) 2-Bromo-4-chloro-4-isopropylpentane
B) 4-Bromo-2-chloro-2-isopropylpentane
C) 5-Bromo-3-chloro-2,3-dimethylhexane
D) 2-Bromo-4-chloro-4,5-dimethylhexane
E) 2-(2-Bromopropyl)-2-chloro-3-methylbutane
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14
How many constitutional isomers are possible for the formula C6H14?

A) 2
B) 3
C) 4
D) 5
E) 6
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15
An IUPAC name for <strong>An IUPAC name for   is:</strong> A) 5-Methyl-4-(1-methylpropyl)hexane B) 2-Methyl-3-(1-methylpropyl)hexane C) 2-Methyl-3-(2-methylpropyl)hexane D) 3-Methyl-4-(1-methylethyl)heptane E) 5-Methyl-4-(1-methylethyl)heptane is:

A) 5-Methyl-4-(1-methylpropyl)hexane
B) 2-Methyl-3-(1-methylpropyl)hexane
C) 2-Methyl-3-(2-methylpropyl)hexane
D) 3-Methyl-4-(1-methylethyl)heptane
E) 5-Methyl-4-(1-methylethyl)heptane
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16
An IUPAC name for the following compound is: <strong>An IUPAC name for the following compound is:  </strong> A) 4-Isobutyl-3,4-dimethylheptane B) 4-sec-Butyl-2,4-dimethylheptane C) 2,4,5-Trimethyl-4-propylheptane D) 3,4,6-Trimethyl-4-propylheptane E) 4-Isobutyl-4,5-dimethylheptane

A) 4-Isobutyl-3,4-dimethylheptane
B) 4-sec-Butyl-2,4-dimethylheptane
C) 2,4,5-Trimethyl-4-propylheptane
D) 3,4,6-Trimethyl-4-propylheptane
E) 4-Isobutyl-4,5-dimethylheptane
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17
What is a correct name for the following compound? <strong>What is a correct name for the following compound?  </strong> A) 3-Isobutyl-2-methylheptane B) 3-sec-Butyl-2-methyloctane C) 5-Isobutyl-6-methylheptane D) 2-Ethyl-3-isopropyloctane E) 4-Isopropyl-3-methylnonane

A) 3-Isobutyl-2-methylheptane
B) 3-sec-Butyl-2-methyloctane
C) 5-Isobutyl-6-methylheptane
D) 2-Ethyl-3-isopropyloctane
E) 4-Isopropyl-3-methylnonane
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18
Isopentyl is the common name for which alkyl group?

A)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)
B)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)
C)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)
D)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)
E)
<strong>Isopentyl is the common name for which alkyl group?</strong> A)   B)   C)   D)   E)
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19
The IUPAC name for <strong>The IUPAC name for   is:</strong> A) 6-Ethyl-3,4-dimethylheptane B) 2-Ethyl-4,5-dimethylheptane C) 3,4,6-Trimethyloctane D) 3,5,6-Trimethyloctane E) 2-(1-Methylpropyl)-4-methylhexane is:

A) 6-Ethyl-3,4-dimethylheptane
B) 2-Ethyl-4,5-dimethylheptane
C) 3,4,6-Trimethyloctane
D) 3,5,6-Trimethyloctane
E) 2-(1-Methylpropyl)-4-methylhexane
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20
Neglecting stereochemistry,which of these common group names is ambiguous,i.e. ,does not refer to one specific group?

A) Butyl
B) sec-Butyl
C) tert-Pentyl
D) Neopentyl
E) sec-Pentyl
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21
Which is the correct name for the compound shown below? <strong>Which is the correct name for the compound shown below?  </strong> A) Bicyclo[2.2.0]hexane B) Bicyclo[2.2.0]butane C) Bicyclo[2.2.2]hexane D) Bicyclo[2.2.1]hexane E) Disquarane

A) Bicyclo[2.2.0]hexane
B) Bicyclo[2.2.0]butane
C) Bicyclo[2.2.2]hexane
D) Bicyclo[2.2.1]hexane
E) Disquarane
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22
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 3-chloro-8-methylbicyclo[4.3.0]nonane B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane D) 3-Methyl-7-chlorobicyclo[4.3.1]decane E) 3-chloro-8-methyl[4.3.0]bicyclononane

A) 3-chloro-8-methylbicyclo[4.3.0]nonane
B) 8-Methyl-3-chlorobicyclo[4.3.1]nonane
C) 3-Methyl-7-chlorobicyclo[4.3.0]nonane
D) 3-Methyl-7-chlorobicyclo[4.3.1]decane
E) 3-chloro-8-methyl[4.3.0]bicyclononane
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23
The most stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The most stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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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24
The least stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The least stable conformation of 2,3-dimethylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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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25
Which compound is a bicycloheptane? <strong>Which compound is a bicycloheptane?  </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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26
The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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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27
What is the correct name of the following compound? <strong>What is the correct name of the following compound?  </strong> A) 1-Chlorobicyclo[4.1.1]octane B) 2-Chlorobicyclo[4.1.0]octane C) 2-Chlorobicyclo[4.1.1]octane D) 2-Chlorobicyclo[4.1.1]heptane E) 5-Chlorobicyclo[4.1.1]octane

A) 1-Chlorobicyclo[4.1.1]octane
B) 2-Chlorobicyclo[4.1.0]octane
C) 2-Chlorobicyclo[4.1.1]octane
D) 2-Chlorobicyclo[4.1.1]heptane
E) 5-Chlorobicyclo[4.1.1]octane
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28
<strong>  Which of the above is bicyclo[4.3.0]nonane?</strong> A) I B) II C) III D) IV E) V
Which of the above is bicyclo[4.3.0]nonane?

A) I
B) II
C) III
D) IV
E) V
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29
What is the name of this compound? <strong>What is the name of this compound?  </strong> A) Bicyclo[2.2.2]octane B) Bicyclo[3.2.1]octane C) Bicyclo[4.1.1]octane D) Bicyclo[4.2.0]octane E) Bicyclo[3.3.0]octane

A) Bicyclo[2.2.2]octane
B) Bicyclo[3.2.1]octane
C) Bicyclo[4.1.1]octane
D) Bicyclo[4.2.0]octane
E) Bicyclo[3.3.0]octane
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30
Which of the following is bicyclo[3.2.2]nonane? <strong>Which of the following is bicyclo[3.2.2]nonane?  </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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31
Which of the following is a correct name which corresponds to the common name tert-pentyl alcohol?

A) 2,2-Dimethyl-1-propanol
B) 2-Ethyl-2-propanol
C) 2-Methyl-2-butanol
D) 3-Methyl-1-butanol
E) Methyl tert-butanol
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32
The correct IUPAC name for the following compound is: <strong>The correct IUPAC name for the following compound is:  </strong> A) 1-Hydroxy-3-sec-butylcyclopentane B) 3-sec-Butyl-1-cyclopentanol C) 1-sec-Butyl-3-cyclopentanol D) 4-sec-Butyl-1-cyclopentanol E) 3-Isobutyl-1-cyclopentanol

A) 1-Hydroxy-3-sec-butylcyclopentane
B) 3-sec-Butyl-1-cyclopentanol
C) 1-sec-Butyl-3-cyclopentanol
D) 4-sec-Butyl-1-cyclopentanol
E) 3-Isobutyl-1-cyclopentanol
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33
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane

A) 4-bromo-3,8-dimethylbicyclo[5.2.2]nonane
B) 3,8-dimethyl-4-bromo-bicyclo[5.2.0]nonane
C) 4-bromo-3,8-dimethylbicyclo[5.2.1]decane
D) 7-bromo-2,6-dimethylbicyclo[5.2.0]nonane
E) 4-bromo-3,8-dimethylbicyclo[5.2.0]nonane
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34
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) 5-Ethyl-3-fluorohexanol B) 5-Ethyl-3-fluoro-1-hexanol C) 2-Ethyl-4-fluoro-6-hexanol D) 3-fluoro-5-methyl-7-heptanol E) 3-fluoro-5-methyl-1-heptanol

A) 5-Ethyl-3-fluorohexanol
B) 5-Ethyl-3-fluoro-1-hexanol
C) 2-Ethyl-4-fluoro-6-hexanol
D) 3-fluoro-5-methyl-7-heptanol
E) 3-fluoro-5-methyl-1-heptanol
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35
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 4-propyl-5-chloro-3-heptanol B) 4-propyl-3-chloro-5-heptanol C) 4-(1-chloropropyl)-3-heptanol D) 5-chloro-4-propyl-3-heptanol E) 3-hydroxy-4-propyl-5-chloroheptane

A) 4-propyl-5-chloro-3-heptanol
B) 4-propyl-3-chloro-5-heptanol
C) 4-(1-chloropropyl)-3-heptanol
D) 5-chloro-4-propyl-3-heptanol
E) 3-hydroxy-4-propyl-5-chloroheptane
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36
A correct name for the following compound is: <strong>A correct name for the following compound is:  </strong> A) 2-Methylbicyclo[4.3.0]nonane B) 1-Methylbicyclo[4.3.1]nonane C) 7-Methylbicyclo[4.3.0]nonane D) 2-Methylbicyclo[4.3.1]nonane E) 1-Methylbicyclo[4.3.0]nonane

A) 2-Methylbicyclo[4.3.0]nonane
B) 1-Methylbicyclo[4.3.1]nonane
C) 7-Methylbicyclo[4.3.0]nonane
D) 2-Methylbicyclo[4.3.1]nonane
E) 1-Methylbicyclo[4.3.0]nonane
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37
<strong>  Which of the above is bicyclo[3.3.1]nonane?</strong> A) I B) II C) III D) IV E) V
Which of the above is bicyclo[3.3.1]nonane?

A) I
B) II
C) III
D) IV
E) V
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38
Which of the following structures represents bicyclo[3.2.1]octane? <strong>Which of the following structures represents bicyclo[3.2.1]octane?  </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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39
<strong>  Which of the above is bicyclo[5.2.0]nonane?</strong> A) I B) II C) III D) IV E) V
Which of the above is bicyclo[5.2.0]nonane?

A) I
B) II
C) III
D) IV
E) V
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40
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back): <strong>The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-2-C-3 bond (i.e. ,C-2 in the front,C-3 in the back):  </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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41
Select the systematic name for <strong>Select the systematic name for  </strong> A) cis-1,3-Dichlorocyclopentane B) trans-1,4-Dichlorocyclopentane C) cis-1,2-Dichlorocyclopentane D) trans-1,3-Dichlorocyclopentane E) 1,1-Dichlorocyclopentane

A) cis-1,3-Dichlorocyclopentane
B) trans-1,4-Dichlorocyclopentane
C) cis-1,2-Dichlorocyclopentane
D) trans-1,3-Dichlorocyclopentane
E) 1,1-Dichlorocyclopentane
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42
Consider the graph below,which is a plot of the relative energies of the various conformations of hexane,viewed through the C-2-C-3 bond.The conformations corresponding to the 60o and 300o are: <strong>Consider the graph below,which is a plot of the relative energies of the various conformations of hexane,viewed through the C-2-C-3 bond.The conformations corresponding to the 60<sup>o</sup> and 300<sup>o</sup> are:  </strong> A) Eclipsed B) Staggered and gauche C) Staggered and anti D) More stable than the conformation at 180<sup>o</sup> E) None of the above

A) Eclipsed
B) Staggered and gauche
C) Staggered and anti
D) More stable than the conformation at 180o
E) None of the above
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43
The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): <strong>The least stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back):  </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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44
Which conformation(s)of 1,2-dibromoethane does not illustrate one or more gauche interactions? <strong>Which conformation(s)of 1,2-dibromoethane does not illustrate one or more gauche interactions?  </strong> A) I and II only B) II,III,and V only C) I,III,and IV only D) All but one above E) All the above

A) I and II only
B) II,III,and V only
C) I,III,and IV only
D) All but one above
E) All the above
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45
The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back): <strong>The most stable conformation of 3-bromo-2-methylpentane,viewed through the C-3-C-4 bond (i.e. ,C-3 in the front,C-4 in the back):  </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
Which is the most stable conformation of cyclohexane?

A) Chair
B) Twist
C) Boat
D) One-half chair
E) Staggered
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47
Consider the graph below,which is a plot of the relative energies of the various conformations of 2,3-dimethylbutane,viewed through the C-2-C-3 bond.The conformations corresponding to the 120o and 240o are: <strong>Consider the graph below,which is a plot of the relative energies of the various conformations of 2,3-dimethylbutane,viewed through the C-2-C-3 bond.The conformations corresponding to the 120<sup>o</sup> and 240<sup>o</sup> are:  </strong> A) Eclipsed,more stable than the conformation at 0<sup>o</sup> B) Eclipsed,more stable than the conformation at 180<sup>o</sup> C) Staggered,more stable than the conformation at 0<sup>o</sup> D) Staggered,less stable than the conformation at 180<sup>o</sup> E) Two of the above are true

A) Eclipsed,more stable than the conformation at 0o
B) Eclipsed,more stable than the conformation at 180o
C) Staggered,more stable than the conformation at 0o
D) Staggered,less stable than the conformation at 180o
E) Two of the above are true
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48
The most stable conformation for 1,2-ethanediol (ethylene glycol)is shown below.It is the most stable conformation because: <strong>The most stable conformation for 1,2-ethanediol (ethylene glycol)is shown below.It is the most stable conformation because:  </strong> A) this corresponds to an anti conformation. B) in general,gauche conformations possess the minimum energy. C) it is stabilized by intramolecular hydrogen bonding. D) it is a staggered conformation. E) it has the highest energy of all the possibilities.

A) this corresponds to an anti conformation.
B) in general,gauche conformations possess the minimum energy.
C) it is stabilized by intramolecular hydrogen bonding.
D) it is a staggered conformation.
E) it has the highest energy of all the possibilities.
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49
The most stable conformation of butane is: <strong>The most stable conformation of butane 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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50
Give the IUPAC name for <strong>Give the IUPAC name for  </strong> A) 3-Methyl-4-hexyne B) 4-Methyl-2-hexyne C) 2-Ethyl-3-pentyne D) 4-Ethyl-2-pentyne E) 3-Methyl-2-hexyne

A) 3-Methyl-4-hexyne
B) 4-Methyl-2-hexyne
C) 2-Ethyl-3-pentyne
D) 4-Ethyl-2-pentyne
E) 3-Methyl-2-hexyne
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51
The least stable conformation of butane is: <strong>The least stable conformation of butane 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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52
The most stable conformation of 1,2-dibromoethane is: <strong>The most stable conformation of 1,2-dibromoethane 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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53
The graph below is a plot of the relative energies of the various conformations of: <strong>The graph below is a plot of the relative energies of the various conformations of:  </strong> A) 2-chloropropane B) 1,3-dichloropropane C) 2-methylpropane D) Butane (C1-C2 rotation) E) Butane (C2-C3 rotation)

A) 2-chloropropane
B) 1,3-dichloropropane
C) 2-methylpropane
D) Butane (C1-C2 rotation)
E) Butane (C2-C3 rotation)
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54
The IUPAC name for diisobutylacetylene is

A) 2,7-Dimethyl-4-octene
B) 2,7-Dimethyl-4-octyne
C) 3,6-Dimethyl-4-octyne
D) 2,5-Diethyl-3-hexyne
E) 2,2,5,5-Tetramethyl-3-hexyne
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55
A correct IUPAC name for the following compound is: <strong>A correct IUPAC name for the following compound is:  </strong> A) 3,6,7-trimethyl-4-bromo-1-octene B) 4-bromo-3-methyl-6-isopropyl-1-heptene C) 4-bromo-3,6,7-trimethyl-1-octene D) 4-bromo-6-isopropyl-3-methyl-1-heptene E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene

A) 3,6,7-trimethyl-4-bromo-1-octene
B) 4-bromo-3-methyl-6-isopropyl-1-heptene
C) 4-bromo-3,6,7-trimethyl-1-octene
D) 4-bromo-6-isopropyl-3-methyl-1-heptene
E) 4-bromo-6-isopropyl-3,6-dimethyl-1-hexene
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56
What is the correct IUPAC name for the following compound? <strong>What is the correct IUPAC name for the following compound?  </strong> A) trans-3-Hydroxymethyl-2-heptene B) trans-2-(1-methylethyl)-4-hexen-1-ol C) trans-5-(1-methylethyl)-2-hexen-6-ol D) cis-5-isopropyl-2,6-hexenol E) cis-2-(1-methylethyl)-4-hepten-1-ol

A) trans-3-Hydroxymethyl-2-heptene
B) trans-2-(1-methylethyl)-4-hexen-1-ol
C) trans-5-(1-methylethyl)-2-hexen-6-ol
D) cis-5-isopropyl-2,6-hexenol
E) cis-2-(1-methylethyl)-4-hepten-1-ol
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57
Which cycloalkane has the greatest ring strain?

A) Cyclopropane
B) Cyclobutane
C) Cyclopentane
D) Cyclohexane
E) Cycloheptane
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58
The graph below is a plot of the relative energies of the various conformations of: <strong>The graph below is a plot of the relative energies of the various conformations of:  </strong> A) Ethane B) Propane C) Chloroethane D) 1-Chloropropane (C1-C2 rotation) E) Butane (C1-C2 rotation)

A) Ethane
B) Propane
C) Chloroethane
D) 1-Chloropropane (C1-C2 rotation)
E) Butane (C1-C2 rotation)
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59
The least stable conformation of cyclohexane is the:

A) boat.
B) twist boat.
C) chair.
D) half-chair.
E) twist chair.
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60
The least stable conformation of butane is: <strong>The least stable conformation of butane 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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61
Which conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane? <strong>Which conformation represents the most stable conformation of trans-1-bromo-4-methylcyclohexane?  </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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62
The most stable conformation of cis-1-tert-butyl-2-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
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63
The most stable conformation of trans-1-tert-butyl-2-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the molecule is in the half chair conformation.
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64
<strong>  trans-1,2-Dibromocyclohexane is represented by structure(s):</strong> A) I B) II C) III D) II and III E) I and II
trans-1,2-Dibromocyclohexane is represented by structure(s):

A) I
B) II
C) III
D) II and III
E) I and II
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65
How many moles of hydrogen (H2)will react with 3-cyclobutylpropan-1-ol?

A) 1
2
B) 2
C) 3
D) 4
E) None of the above
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66
What structure represents the most stable conformation of cis-1,3-dimethylcyclohexane? <strong>What structure represents the most stable conformation of cis-1,3-dimethylcyclohexane?  </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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67
Select the structure for cis-3-methyl-6-vinylcyclohexene. <strong>Select the structure for cis-3-methyl-6-vinylcyclohexene.  </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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68
Catalytic hydrogenation of which of the following will yield 2-methylpentane?

A) 2-methyl-1-pentene
2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above
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69
In the most stable conformation of cis-1,4-dimethylcyclohexane,the methyl groups are:

A) one axial,one equatorial.
B) both axial.
C) both equatorial.
D) alternating between being both axial and both equatorial.
E) None of the above
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70
Which of these C10H18 isomers is predicted to be the most stable? <strong>Which of these C<sub>10</sub>H<sub>18</sub> isomers is predicted to be the most stable?  </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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71
Which of the following will have the same energy after undergoing ring flip? <strong>Which of the following will have the same energy after undergoing ring flip?  </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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72
The twist boat conformation is the preferred conformation for this compound.

A) cis-1,4-Di-tert-butylcyclohexane
B) trans-1,4-Di-tert-butylcyclohexane
C) cis-1,3-Di-tert-butylcyclohexane
D) trans-1,2-Di-tert-butylcyclohexane
E) None of these
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73
How many moles of hydrogen (H2)will react with (trans,trans)-hepta-3,5-dien-1-yne?

A) 1
2
B) 2
C) 3
D) 4
E) 5
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74
The most stable conformation of trans-1-tert-butyl-3-methylcyclohexane is the one in which:

A) the tert-butyl group is axial and the methyl group is equatorial.
B) the methyl group is axial and the tert-butyl group is equatorial.
C) both groups are axial.
D) both groups are equatorial.
E) the twist boat conformation is adopted.
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75
cis-1,3-Dibromocyclohexane is represented by structure(s): <strong>cis-1,3-Dibromocyclohexane is represented by structure(s):  </strong> A) I B) II C) III D) II and III E) I and II

A) I
B) II
C) III
D) II and III
E) I and II
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76
Which of the following can be described as trans isomers? <strong>Which of the following can be described as trans isomers?   </strong> A) I B) II,V C) III,IV D) I,III and IV E) None of the above are trans isomers.

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are trans isomers.
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77
<strong>  cis-1,2-Dibromocyclohexane is represented by structure(s):</strong> A) I B) II C) III D) II and III E) I and II
cis-1,2-Dibromocyclohexane is represented by structure(s):

A) I
B) II
C) III
D) II and III
E) I and II
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78
Select the reagents necessary to convert cyclopentene into cyclopentane.

A) H2 and Ni
B) H2O
C) Heat
D) Zn,H3O+
E) Light
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79
Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?

A)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)
B)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)
C)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)
D)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)
E)
<strong>Which alkene would yield 3-methylpentane when subjected to catalytic hydrogenation?</strong> A)   B)   C)   D)   E)
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80
Which of the following can be described as cis isomers? <strong>Which of the following can be described as cis isomers?  </strong> A) I B) II,V C) III,IV D) I,III and IV E) None of the above are cis isomers.

A) I
B) II,V
C) III,IV
D) I,III and IV
E) None of the above are cis isomers.
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