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As pointed out in the comments to this question, cyclic hydrocarbons have higher boiling points than their acyclic isomers. The major attractive force for hydrocarbons should be the London forces, which scale with surface area. My intuition has me thinking the cyclic molecules have less surface area, but they might enable more productive interactions over larger parts of their surface area due to their fixed conformations. I would love to see a study or some data that supports my intuition.

Boiling point data

Three carbons

Four carbons

Five carbons

Six carbons

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Your intuition is indeed correct! Several sources provide the same answer (1, 2, 3). Perhaps the simplest and most direct evidence comes from comparing the densities of the liquid unbranched alkanes and cycloalkanes:

enter image description here

(Source)

The cycloalkanes have slightly lower molecular mass than their parent unbranched alkanes with the same number of carbon atoms, yet the cycloalkanes are consistently more dense in the liquid phase by a factor of ~20%. The only way this can happen is if each individual cycloalkane molecule effectively occupies less volume in the liquid phase than the related alkane. This means cycloalkane molecules are closer on average in the liquid, and as van der Waals forces are attractive (at intermolecular separations) and their strength varies inversely with distance, the intermolecular attractions are stronger in cycloalkanes, and so the boiling point of the cycloalkanes should be higher.

This can be explained by considering that the unbranched linear chains in alkanes have many possible conformations, and thus are in more geometrically irregular contact in the liquid, leaving more space on average between the molecules. Cycloalkanes do not have as many conformations available, and so their molecules will approach each other more orderly and effectively, leaving less intermolecular space.

Presumably this effect can be extended to all substances (including the ethers mentioned in the question you linked), but it need not always be the dominant factor in determining boiling points.

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    $\begingroup$ The relation to density is certainly compelling. I'm wondering if there is any computational data that can be present on the relative surface areas (or perhaps more importantly surface area to volume ratios). $\endgroup$ – Ben Norris Jun 3 '15 at 21:23
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    $\begingroup$ It should be pointed out that the type of molecular volume I mention (macroscopic volume occupied by liquid divided by number of molecules present = effective molecular volume) is not equivalent to the volume most often mentioned in computational chemistry, which is the region enclosed by the van der Waals surface. The only way to obtain the effective molecular volume would be to simulate a large box filled with molecules at a temperature high enough for them to be liquid, and not just by calculating the geometry of a single molecule. $\endgroup$ – Nicolau Saker Neto Jun 3 '15 at 21:38
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I agree with the points made above regarding attractive forces in the liquid being diminished in the gas phase.

However, I also think there may be an entropic component to all of this. When a molecule undergoes a phase change from liquid to gas (e.g. it boils)

$$\Delta G_\mathrm{vap} = \Delta H_\mathrm{vap} - T_\mathrm{vap} \times \Delta S_\mathrm{vap} = 0$$

or

$$\frac{\Delta H_\mathrm{vap}}{T_\mathrm{vap}} = \Delta S_\mathrm{vap}$$

For a ring, torsional vibrations (rotations about the $\ce{C-C}$ single bonds) are constrained in both the liquid and gas phase compared to an acyclic analogue where there is free rotation about the single bonds. Hence, we would expect $\Delta S_\mathrm{vap}$ to be smaller for a cyclic compound compared to a noncyclic analogue. For $\Delta S_\mathrm{vap}$ to be smaller either $T$ must be larger (higher boiling point) and/or $\Delta H_\mathrm{vap}$ must be smaller.

It's easy to see how the arguments presented in the other answers can produce an increase in the enthalpic term for rings, but this would tend to move $\Delta S_\mathrm{vap}$ in the wrong direction to completely explain the effect (e.g. $\Delta S_\mathrm{vap}$ would be larger for the rings than non-rings).

Therefore, when comparing compounds like cyclopentane and pentane, I suspect that the enthalpic term for the ring is similar to or larger than that for the non-ring. Yet since the entropic term is smaller for the ring compared to the non-ring, this requires that $T$ must be larger for the ring compared to the non-ring. In other words, the boiling point for the ring will be higher than the boiling point of the non-ring. Also, this reasoning would explain why, as rings get larger and are able to rotate about their bonds more freely, the magnitude of the difference between rings and non-rings diminishes.

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    $\begingroup$ Also of interest would be to consider even more conformationally restricted molecules, such as polycyclic saturated hydrocarbons (decalin, norbornane, etc). Data on these are significantly sparser, though. $\endgroup$ – Nicolau Saker Neto Jun 3 '15 at 21:54
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The best that I have been able to determine is that it has to do with the rigidity of the rings. With the rings locked into certain conformations, the molecules are able to come into closer contact, as the movement of the chains in the non ring compounds can clear a larger around the molecules. Rings, on the other hands, are locked into certain conformations, so their area of contact is consistently larger.

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    $\begingroup$ This is probably on the right track. My intuition tells me this also, but I would love to see some data that would back it up. $\endgroup$ – Ben Norris Jun 3 '15 at 20:17
  • $\begingroup$ Stated slightly differently - the rings aren't able to spin (as much) about their carbon-carbon bond to dislodge a neighboring molecule. $\endgroup$ – Ryan Ward Jun 8 '16 at 14:03

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