Deck 6: Isomerism 1: Conformational and Constitutional Isomers

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Question
Rank the steric strain of the following types of conformations from highest energy to lowest energy.

A)Anti > eclipsed > gauche
B)Eclipsed > anti > gauche
C)Gauche > anti > eclipsed
D)Eclipsed > gauche > anti
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Question
Which of the following compounds has/have substituents cis to each other? <strong>Which of the following compounds has/have substituents cis to each other?  </strong> A)I B)II C)III D)IV E)II and IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)II and IV
Question
How many fluorine atoms are in equatorial positions in the following chair structure? <strong>How many fluorine atoms are in equatorial positions in the following chair structure?  </strong> A)One B)Two C)Three D)Four E)Five <div style=padding-top: 35px>

A)One
B)Two
C)Three
D)Four
E)Five
Question
Which of the following dash-wedge structures best represents the Newman projection below? <strong>Which of the following dash-wedge structures best represents the Newman projection below?  </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 least stable cyclohexane conformation?

A)Chair
B)Half-chair
C)Twist-boat
D)Boat
E)Crown
Question
Which of the following dash-wedge structures best represents the Newman projection below? <strong>Which of the following dash-wedge structures best represents the Newman projection below?  </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 largest molar heat of combustion? <strong>Which of the following molecules has the largest molar heat of combustion?  </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 substituents are gauche to each other? <strong>Which substituents are gauche to each other?  </strong> A)I and Br B)I and OH C)CH<sub>3</sub> and Br D)H and I E)Cl and Br <div style=padding-top: 35px>

A)I and Br
B)I and OH
C)CH3 and Br
D)H and I
E)Cl and Br
Question
The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)? <strong>The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)?  </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 Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)? <strong>The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)?  </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 conformer is highest in energy? <strong>Which conformer is highest in energy?  </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 Newman projection results from rotating the front carbon 240° clockwise? <strong>Which Newman projection results from rotating the front carbon 240° clockwise?  </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 pairs do not have the same connectivity?

A)Two stereoisomers
B)Two conformational isomers
C)Cyclohexane chair conformations before and after a chair flip
D)Two constitutional isomers
E)Two Newman projection rotamers
Question
Which of the following has the least ring strain? <strong>Which of the following has the least ring strain?  </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 substituents are anti to each other? <strong>Which substituents are anti to each other?  </strong> A)OCH<sub>3</sub> and H B)Cl and CH<sub>2</sub>CH<sub>3</sub> C)Br and SH D)H and Cl E)CH<sub>2</sub>CH<sub>3</sub> and Br <div style=padding-top: 35px>

A)OCH3 and H
B)Cl and CH2CH3
C)Br and SH
D)H and Cl
E)CH2CH3 and Br
Question
Which of the following types of isomer differs only by the rotation about single bonds?

A)Constitutional
B)Configurational
C)Conformational
D)Diastereomers
E)Enantiomers
Question
Which of the following Newman projections is least stable? <strong>Which of the following Newman projections is least stable?  </strong> A)I B)II C)III D)IV E)All are equally stable. <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)All are equally stable.
Question
How many degrees does the front carbon have to be rotated clockwise to result in a gauche conformer? <strong>How many degrees does the front carbon have to be rotated clockwise to result in a gauche conformer?  </strong> A)60° B)90° C)109.5° D)120° E)300° <div style=padding-top: 35px>

A)60°
B)90°
C)109.5°
D)120°
E)300°
Question
Which structure best represents the following disubstituted cyclohexane? <strong>Which structure best represents the following disubstituted cyclohexane?  </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 molecule represents the chair-flipped conformer of the given compound? <strong>Which molecule represents the chair-flipped conformer of the given compound?  </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
Calculate the index of hydrogen deficiency for the following formula: C8H12NOF2-.

A)0
B)1
C)2
D)3
E)4
Question
Which set of molecules does not consist of constitutional isomers? <strong>Which set of molecules does not consist of constitutional isomers?  </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 isomers is most stable? <strong>Which of the following isomers is most stable?  </strong> A)I B)II C)III D)IV E)I, II, and III have the same stability and are more stable than IV. <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
E)I, II, and III have the same stability and are more stable than IV.
Question
Which is the most stable conformation of the given trisubstituted cyclohexane below? <strong>Which is the most stable conformation of the given trisubstituted cyclohexane below?  </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 set of molecules are not considered constitutional isomers? <strong>Which set of molecules are not considered constitutional isomers?  </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
Perform a conformational analysis of 1,1-dichloropropane looking down the C1C2 bond.
Question
Draw a constitutional isomer for the following compound. Draw a constitutional isomer for the following compound.  <div style=padding-top: 35px>
Question
Draw the least stable Newman projection for 1-iodobutane looking down the C1C2 bond.
Question
Conformational isomers differ by __________.
Question
Which is the most stable chair conformation of the following Haworth projection? <strong>Which is the most stable chair conformation of the following Haworth projection?  </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
Perform a conformational analysis of bromoethane looking down the C1C2 bond.
Question
Draw the dash-wedge structure that corresponds to the following Newman projection. Draw the dash-wedge structure that corresponds to the following Newman projection.  <div style=padding-top: 35px>
Question
Draw the dash-wedge structure that corresponds to the following Newman projection. Draw the dash-wedge structure that corresponds to the following Newman projection.  <div style=padding-top: 35px>
Question
Which Haworth projection corresponds to the following chair conformation? <strong>Which Haworth projection corresponds to the following chair conformation?  </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 chair conformations is lowest in energy? <strong>Which of the following chair conformations is lowest in energy?  </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 IHD? <strong>Which of the following molecules has the highest IHD?  </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
Draw the Newman projection that corresponds to the following species. Draw the Newman projection that corresponds to the following species.  <div style=padding-top: 35px>
Question
Draw the Newman projection for the following species. Draw the Newman projection for the following species.  <div style=padding-top: 35px>
Question
What is the most stable chair conformation for the following molecule? <strong>What is the most stable chair conformation for the following molecule?  </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
Draw the most stable Newman projection for 1-bromo-2-chloroethane.
Question
Calculate the IHD for the formula C7H11BrO.
Question
Draw the following molecule after it undergoes a chair flip. Draw the following molecule after it undergoes a chair flip.  <div style=padding-top: 35px>
Question
Draw six constitutional isomers for C4H11N.
Question
Draw the most stable chair conformation for the following molecule. Draw the most stable chair conformation for the following molecule.  <div style=padding-top: 35px>
Question
Draw a Haworth projection for the following trisubstituted cyclohexane Draw a Haworth projection for the following trisubstituted cyclohexane  <div style=padding-top: 35px>
Question
Clearly draw the following molecule with all of its substituents in axial positions. Clearly draw the following molecule with all of its substituents in axial positions.  <div style=padding-top: 35px>
Question
Explain why cyclohexane has less ring strain than cyclopropane.
Question
Draw the most Newman projection for 1-iodobutane looking down the C1-C2 bond.
Question
How many of the following chair conformations have CH3 groups that are trans to each other? How many of the following chair conformations have CH<sub>3 </sub>groups that are trans to each other?  <div style=padding-top: 35px>
Question
Draw a chair structure for the following Haworth structure. Draw a chair structure for the following Haworth structure.  <div style=padding-top: 35px>
Question
Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain. Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.  <div style=padding-top: 35px>
Question
Clearly draw the most stable conformer of the following molecule in chair formation. Clearly draw the most stable conformer of the following molecule in chair formation.  <div style=padding-top: 35px>
Question
A molecule has two rings,three double bonds,and two triple bonds.How many IHD units does this molecule have?
Question
What is the IHD for the formula C8H17NOClF?
Question
How many CH3 CH3 gauche interactions are present in the following Newman projection? How many CH<sub>3 </sub><font face=symbol></font>CH<sub>3</sub> gauche interactions are present in the following Newman projection?  <div style=padding-top: 35px>
Question
Label each of the following molecules as cis or trans. Label each of the following molecules as cis or trans.  <div style=padding-top: 35px>
Question
Draw all alkyne-containing isomers of C5H8.
Question
Give five constitutional isomers for the formula C4H6.
Question
Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain. Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.  <div style=padding-top: 35px>
Question
Draw the most stable chair conformation for the following compound. Draw the most stable chair conformation for the following compound.  <div style=padding-top: 35px>
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Deck 6: Isomerism 1: Conformational and Constitutional Isomers
1
Rank the steric strain of the following types of conformations from highest energy to lowest energy.

A)Anti > eclipsed > gauche
B)Eclipsed > anti > gauche
C)Gauche > anti > eclipsed
D)Eclipsed > gauche > anti
Eclipsed > gauche > anti
2
Which of the following compounds has/have substituents cis to each other? <strong>Which of the following compounds has/have substituents cis to each other?  </strong> A)I B)II C)III D)IV E)II and IV

A)I
B)II
C)III
D)IV
E)II and IV
II and IV
3
How many fluorine atoms are in equatorial positions in the following chair structure? <strong>How many fluorine atoms are in equatorial positions in the following chair structure?  </strong> A)One B)Two C)Three D)Four E)Five

A)One
B)Two
C)Three
D)Four
E)Five
Three
4
Which of the following dash-wedge structures best represents the Newman projection below? <strong>Which of the following dash-wedge structures best represents the Newman projection below?  </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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5
Which is the least stable cyclohexane conformation?

A)Chair
B)Half-chair
C)Twist-boat
D)Boat
E)Crown
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6
Which of the following dash-wedge structures best represents the Newman projection below? <strong>Which of the following dash-wedge structures best represents the Newman projection below?  </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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7
Which of the following molecules has the largest molar heat of combustion? <strong>Which of the following molecules has the largest molar heat of combustion?  </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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8
Which substituents are gauche to each other? <strong>Which substituents are gauche to each other?  </strong> A)I and Br B)I and OH C)CH<sub>3</sub> and Br D)H and I E)Cl and Br

A)I and Br
B)I and OH
C)CH3 and Br
D)H and I
E)Cl and Br
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9
The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)? <strong>The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)?  </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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10
The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)? <strong>The Newman projection looking down the indicated bond in the species below is best represented by which of the following (I,II,III,IV,or V)?  </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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11
Which conformer is highest in energy? <strong>Which conformer is highest in energy?  </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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12
Which Newman projection results from rotating the front carbon 240° clockwise? <strong>Which Newman projection results from rotating the front carbon 240° clockwise?  </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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13
Which of the following pairs do not have the same connectivity?

A)Two stereoisomers
B)Two conformational isomers
C)Cyclohexane chair conformations before and after a chair flip
D)Two constitutional isomers
E)Two Newman projection rotamers
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14
Which of the following has the least ring strain? <strong>Which of the following has the least ring strain?  </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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15
Which substituents are anti to each other? <strong>Which substituents are anti to each other?  </strong> A)OCH<sub>3</sub> and H B)Cl and CH<sub>2</sub>CH<sub>3</sub> C)Br and SH D)H and Cl E)CH<sub>2</sub>CH<sub>3</sub> and Br

A)OCH3 and H
B)Cl and CH2CH3
C)Br and SH
D)H and Cl
E)CH2CH3 and Br
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16
Which of the following types of isomer differs only by the rotation about single bonds?

A)Constitutional
B)Configurational
C)Conformational
D)Diastereomers
E)Enantiomers
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17
Which of the following Newman projections is least stable? <strong>Which of the following Newman projections is least stable?  </strong> A)I B)II C)III D)IV E)All are equally stable.

A)I
B)II
C)III
D)IV
E)All are equally stable.
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18
How many degrees does the front carbon have to be rotated clockwise to result in a gauche conformer? <strong>How many degrees does the front carbon have to be rotated clockwise to result in a gauche conformer?  </strong> A)60° B)90° C)109.5° D)120° E)300°

A)60°
B)90°
C)109.5°
D)120°
E)300°
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19
Which structure best represents the following disubstituted cyclohexane? <strong>Which structure best represents the following disubstituted cyclohexane?  </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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20
Which molecule represents the chair-flipped conformer of the given compound? <strong>Which molecule represents the chair-flipped conformer of the given compound?  </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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21
Calculate the index of hydrogen deficiency for the following formula: C8H12NOF2-.

A)0
B)1
C)2
D)3
E)4
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22
Which set of molecules does not consist of constitutional isomers? <strong>Which set of molecules does not consist of constitutional isomers?  </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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23
Which of the following isomers is most stable? <strong>Which of the following isomers is most stable?  </strong> A)I B)II C)III D)IV E)I, II, and III have the same stability and are more stable than IV.

A)I
B)II
C)III
D)IV
E)I, II, and III have the same stability and are more stable than IV.
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24
Which is the most stable conformation of the given trisubstituted cyclohexane below? <strong>Which is the most stable conformation of the given trisubstituted cyclohexane below?  </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 set of molecules are not considered constitutional isomers? <strong>Which set of molecules are not considered constitutional isomers?  </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
Perform a conformational analysis of 1,1-dichloropropane looking down the C1C2 bond.
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27
Draw a constitutional isomer for the following compound. Draw a constitutional isomer for the following compound.
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28
Draw the least stable Newman projection for 1-iodobutane looking down the C1C2 bond.
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29
Conformational isomers differ by __________.
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30
Which is the most stable chair conformation of the following Haworth projection? <strong>Which is the most stable chair conformation of the following Haworth projection?  </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
Perform a conformational analysis of bromoethane looking down the C1C2 bond.
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32
Draw the dash-wedge structure that corresponds to the following Newman projection. Draw the dash-wedge structure that corresponds to the following Newman projection.
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33
Draw the dash-wedge structure that corresponds to the following Newman projection. Draw the dash-wedge structure that corresponds to the following Newman projection.
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34
Which Haworth projection corresponds to the following chair conformation? <strong>Which Haworth projection corresponds to the following chair conformation?  </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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35
Which of the following chair conformations is lowest in energy? <strong>Which of the following chair conformations is lowest in energy?  </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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36
Which of the following molecules has the highest IHD? <strong>Which of the following molecules has the highest IHD?  </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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37
Draw the Newman projection that corresponds to the following species. Draw the Newman projection that corresponds to the following species.
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38
Draw the Newman projection for the following species. Draw the Newman projection for the following species.
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39
What is the most stable chair conformation for the following molecule? <strong>What is the most stable chair conformation for the following molecule?  </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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40
Draw the most stable Newman projection for 1-bromo-2-chloroethane.
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41
Calculate the IHD for the formula C7H11BrO.
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42
Draw the following molecule after it undergoes a chair flip. Draw the following molecule after it undergoes a chair flip.
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43
Draw six constitutional isomers for C4H11N.
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44
Draw the most stable chair conformation for the following molecule. Draw the most stable chair conformation for the following molecule.
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45
Draw a Haworth projection for the following trisubstituted cyclohexane Draw a Haworth projection for the following trisubstituted cyclohexane
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46
Clearly draw the following molecule with all of its substituents in axial positions. Clearly draw the following molecule with all of its substituents in axial positions.
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47
Explain why cyclohexane has less ring strain than cyclopropane.
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48
Draw the most Newman projection for 1-iodobutane looking down the C1-C2 bond.
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49
How many of the following chair conformations have CH3 groups that are trans to each other? How many of the following chair conformations have CH<sub>3 </sub>groups that are trans to each other?
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50
Draw a chair structure for the following Haworth structure. Draw a chair structure for the following Haworth structure.
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51
Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain. Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.
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52
Clearly draw the most stable conformer of the following molecule in chair formation. Clearly draw the most stable conformer of the following molecule in chair formation.
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53
A molecule has two rings,three double bonds,and two triple bonds.How many IHD units does this molecule have?
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54
What is the IHD for the formula C8H17NOClF?
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55
How many CH3 CH3 gauche interactions are present in the following Newman projection? How many CH<sub>3 </sub><font face=symbol></font>CH<sub>3</sub> gauche interactions are present in the following Newman projection?
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56
Label each of the following molecules as cis or trans. Label each of the following molecules as cis or trans.
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57
Draw all alkyne-containing isomers of C5H8.
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58
Give five constitutional isomers for the formula C4H6.
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59
Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain. Would the cis or trans isomer be more stable for the following disubstituted cyclohexane? Explain.
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60
Draw the most stable chair conformation for the following compound. Draw the most stable chair conformation for the following compound.
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