Term
the general formula for cycloalkanes that have 1 ring |
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Definition
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Term
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Definition
1: find the parent 2: number the substituents |
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Term
how to find the parent in a cycloalkane |
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Definition
-if the number of C atoms in a ring is larger than the number in the largest substituent, the compound is named as an alkyl-substituted cycloalkane -if the number of C atoms in the ring is smaller than the number in the largest substituent, the compound is named as a cycloalkyl-substituted alkane |
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Term
alkyl-substituted cycloalkane |
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Definition
cycloalkane where the # of C atoms in the ring is larger than the number in the largest substituent |
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Term
cycloalkyl-substituted alkane |
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Definition
cycloalkane where the # of C atoms in the ring is smaller than the number in the largest substituent |
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Term
how to number the substituents in a cycloalkane |
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Definition
1: start at a point of attachment and number the substituents so that the second substituent has the lowest possible number 2: if necessary, proceed until a point of difference is found 3: if 2 or more substituents might potentially receive the same number, number them by alphabetical priority 4: halogens are treated in the same way as alkyl groups |
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Term
size of a cycloalkane's ring vs. amount of rotational freedom |
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Definition
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Term
cis-disubstituted cycloalkane ring |
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Definition
has 2 substituents on the same side of the ring |
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Term
trans-disubstituted cycloalkane ring |
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Definition
has 2 substituents on opposite sides of the ring |
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Term
general principles of conformation of cycloalkanes |
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Definition
1: ring strain 2: heats of combustion of cycloalkanes 3: the nature of ring strain |
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Term
how to measure the strain in cycloalkanes |
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Definition
measure the total energy of a compound and compare it to a strain-free reference compound |
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Term
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Definition
the amount of heat released when a compound is completely burned in oxygen |
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Term
amount of strain vs. heat of combustion |
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Definition
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Term
how strain a per CJH2 unit can be calculated and plotted |
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Definition
as a function of ring size |
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Term
the rings that have serious strain |
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Definition
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Term
rings tend to adopt these conformations |
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Definition
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Term
factors that account for ring strain |
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Definition
-angle strain occurs when bond angles are distorted from their normal values -torsional strain is due to eclipsing of bonds -steric strain results when atoms approach too closely |
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Term
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Definition
occurs when bond angles are distorted from their normal values |
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Term
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Definition
caused by eclipsing of bonds |
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Term
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Definition
results when atoms approach too closely |
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Term
some small cycloalkane rings |
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Definition
-cyclopropane -cyclobutane -cyclopentane |
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Term
why cyclopropane is more reactive than other cycloalkanes |
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Definition
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Term
what cyclopentane does to relieve torsional strain |
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Definition
adopts a puckered conformation |
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Term
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Definition
in this conformation, one C is bent out of plane and the H's are nearly staggered |
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Term
a conformation of cyclohexane |
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Definition
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Term
where the bonds are in chair conformation cyclohexane |
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Definition
lower bonds in front and upper bonds in back |
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Term
the strain in chair conformation cyclohexane |
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Definition
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Term
the strain that results when chair conformation cyclohexane converts to boat conformation cyclohexane |
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Definition
has little ange strain, but experiences both steric and torsional strain |
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Term
the 2 kinds of positions on a cyclohexane ring |
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Definition
-6 axial H's -6 equatorial H's |
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Term
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Definition
perpendicular to the plane of the ring |
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Term
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Definition
roughly in the same plane of the ring |
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Term
the orientation of the H's of each C in cyclohexane |
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Definition
each C has 1 axial H and 1 equatorial H |
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Term
orientation of the H's on the side of the ring in cyclohexane |
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Definition
each side of the ring has alternating axial and equatorial H's |
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Term
if all the H's in a cyclohexane ring are on the same face, they are... |
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Definition
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Term
how different chair conformations of cyclohexanes interconvert |
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Definition
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Term
what a ring flip does to the axial and equatorial bonds in cyclohexane |
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Definition
an axial bond becomes equatorial and an equatorial bond becomes axial |
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Term
the energy barrier to conversion in cyclohexane |
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Definition
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Term
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Definition
interactions between an axial group and a ring H 2 C's away |
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Term
what causes diaxial interactions? |
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Definition
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Term
the interactions that occur in gauche butane |
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Definition
diaxial interactions caused by steric energy |
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Term
the position in which substituents on a cycloalkane are more stable |
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Definition
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Term
the size of the strain between substituents in a cyclohexane depends on... |
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Definition
the size and nature of the group |
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Term
the orientation of the substituents in the chair conformations of a cis isomer |
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Definition
one is axial and the other is equatorial |
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Term
the orientation of the substituents in the chair conformations of a trans isomer |
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Definition
both are either axial or equatorial |
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Term
why axial orientation is less stable than equatorial orientation |
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Definition
because there's diaxial interactions in the axial orientation |
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Term
2 ways cycloalkane rings can be fused |
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Definition
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Term
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Definition
have rings that are connected by bridges |
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Term
the general formula for cycloalkanes that have 1 ring |
|
Definition
|
|
Term
|
Definition
1: find the parent 2: number the substituents |
|
|
Term
how to find the parent in a cycloalkane |
|
Definition
-if the number of C atoms in a ring is larger than the number in the largest substituent, the compound is named as an alkyl-substituted cycloalkane -if the number of C atoms in the ring is smaller than the number in the largest substituent, the compound is named as a cycloalkyl-substituted alkane |
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Term
alkyl-substituted cycloalkane |
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Definition
cycloalkane where the # of C atoms in the ring is larger than the number in the largest substituent |
|
|
Term
cycloalkyl-substituted alkane |
|
Definition
cycloalkane where the # of C atoms in the ring is smaller than the number in the largest substituent |
|
|
Term
how to number the substituents in a cycloalkane |
|
Definition
1: start at a point of attachment and number the substituents so that the second substituent has the lowest possible number 2: if necessary, proceed until a point of difference is found 3: if 2 or more substituents might potentially receive the same number, number them by alphabetical priority 4: halogens are treated in the same way as alkyl groups |
|
|
Term
size of a cycloalkane's ring vs. amount of rotational freedom |
|
Definition
|
|
Term
cis-disubstituted cycloalkane ring |
|
Definition
has 2 substituents on the same side of the ring |
|
|
Term
trans-disubstituted cycloalkane ring |
|
Definition
has 2 substituents on opposite sides of the ring |
|
|
Term
general principles of conformation of cycloalkanes |
|
Definition
1: ring strain 2: heats of combustion of cycloalkanes 3: the nature of ring strain |
|
|
Term
how to measure the strain in cycloalkanes |
|
Definition
measure the total energy of a compound and compare it to a strain-free reference compound |
|
|
Term
|
Definition
the amount of heat released when a compound is completely burned in oxygen |
|
|
Term
amount of strain vs. heat of combustion |
|
Definition
|
|
Term
how strain a per CJH2 unit can be calculated and plotted |
|
Definition
as a function of ring size |
|
|
Term
the rings that have serious strain |
|
Definition
|
|
Term
rings tend to adopt these conformations |
|
Definition
|
|
Term
factors that account for ring strain |
|
Definition
-angle strain occurs when bond angles are distorted from their normal values -torsional strain is due to eclipsing of bonds -steric strain results when atoms approach too closely |
|
|
Term
|
Definition
occurs when bond angles are distorted from their normal values |
|
|
Term
|
Definition
caused by eclipsing of bonds |
|
|
Term
|
Definition
results when atoms approach too closely |
|
|
Term
some small cycloalkane rings |
|
Definition
-cyclopropane -cyclobutane -cyclopentane |
|
|
Term
why cyclopropane is more reactive than other cycloalkanes |
|
Definition
|
|
Term
what cyclopentane does to relieve torsional strain |
|
Definition
adopts a puckered conformation |
|
|
Term
|
Definition
in this conformation, one C is bent out of plane and the H's are nearly staggered |
|
|
Term
a conformation of cyclohexane |
|
Definition
|
|
Term
where the bonds are in chair conformation cyclohexane |
|
Definition
lower bonds in front and upper bonds in back |
|
|
Term
the strain in chair conformation cyclohexane |
|
Definition
|
|
Term
the strain that results when chair conformation cyclohexane converts to boat conformation cyclohexane |
|
Definition
has little ange strain, but experiences both steric and torsional strain |
|
|
Term
the 2 kinds of positions on a cyclohexane ring |
|
Definition
-6 axial H's -6 equatorial H's |
|
|
Term
|
Definition
perpendicular to the plane of the ring |
|
|
Term
|
Definition
roughly in the same plane of the ring |
|
|
Term
the orientation of the H's of each C in cyclohexane |
|
Definition
each C has 1 axial H and 1 equatorial H |
|
|
Term
orientation of the H's on the side of the ring in cyclohexane |
|
Definition
each side of the ring has alternating axial and equatorial H's |
|
|
Term
if all the H's in a cyclohexane ring are on the same face, they are... |
|
Definition
|
|
Term
how different chair conformations of cyclohexanes interconvert |
|
Definition
|
|
Term
what a ring flip does to the axial and equatorial bonds in cyclohexane |
|
Definition
an axial bond becomes equatorial and an equatorial bond becomes axial |
|
|
Term
the energy barrier to conversion in cyclohexane |
|
Definition
|
|
Term
|
Definition
interactions between an axial group and a ring H 2 C's away |
|
|
Term
what causes diaxial interactions? |
|
Definition
|
|
Term
the interactions that occur in gauche butane |
|
Definition
diaxial interactions caused by steric energy |
|
|
Term
the position in which substituents on a cycloalkane are more stable |
|
Definition
|
|
Term
the size of the strain between substituents in a cyclohexane depends on... |
|
Definition
the size and nature of the group |
|
|
Term
the orientation of the substituents in the chair conformations of a cis isomer |
|
Definition
one is axial and the other is equatorial |
|
|
Term
the orientation of the substituents in the chair conformations of a trans isomer |
|
Definition
both are either axial or equatorial |
|
|
Term
why axial orientation is less stable than equatorial orientation |
|
Definition
because there's diaxial interactions in the axial orientation |
|
|
Term
2 ways cycloalkane rings can be fused |
|
Definition
|
|
Term
|
Definition
have rings that are connected by bridges |
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