English

Noun

1. Any saturated alicyclic hydrocarbon.

Related terms

• cyclopropane
• cyclobutane
• cyclopentane
• cyclohexane
• cycloheptane

Translations

See also

• alkane
• benzene

Cycloalkanes (also called naphthenes, especially if from petroleum sources) are types of alkanes which have one or more rings of carbon atoms in the chemical structure of their molecules. Alkanes are types of organic hydrocarbon compounds which have only single chemical bonds in their chemical structure. Cycloalkanes consist of only carbon (C) and hydrogen (H) atoms and are saturated because there are no multiple C-C bonds to hydrogenate (add more hydrogen to). A general chemical formula for cycloalkanes would be CnH2(n+1-g) where n = number of C atoms and g = number of rings in the molecule. Cycloalkanes with a single ring are named analogously to their normal alkane counterpart of the same carbon count: cyclopropane, cyclobutane, cyclopentane, cyclohexane, etc. The larger cycloalkanes, with greater than 20 carbon atoms are typically called cycloparaffins.

Cycloalkanes are classified into small, normal and bigger cycloalkanes, where cyclopropane and cyclobutane are the small ones, cyclopentane, cyclohexane, cycloheptane are the normal ones, and the rest are the bigger ones.

Nomenclature

See also: IUPAC nomenclature

The naming of polycyclic alkanes such as bicyclic alkanes and spiro alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings (e.g., "bicyclo"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of vertices. For instance, a bicyclooctane that consists of a six-member ring and a four-member ring, which share two adjacent carbon atoms that form a shared edge, is [4.2.0]-bicyclooctane. That part of the six-member ring, exclusive of the shared edge has 4 carbons. That part of the four-member ring, exclusive of the shared edge, has 2 carbons. The edge itself, exclusive of the two vertices that define it, has 0 carbons.

The group of cycloalkanes are also known as naphthenes, as they are compounds of petroleum or naphtha.

Properties

Cycloalkanes are similar to alkanes in their general physical properties, but they have higher boiling points, melting points, and densities than alkanes. This is due to stronger London forces because the ring shape allows for a larger area of contact. Cycloalkanes exhibit almost the same degree of unreactivity as alkanes, due to their containing only unreactive C-C and C-H bonds; however, the ring strain (see below) can cause cycloalkanes to be more reactive.

Ring strain

The carbon atoms in cycloalkanes are sp3 hybridized and are therefore a deviation from the ideal tetrahedral bond angles of 109.47 degrees. This causes an increase in potential energy and an overall destabilizing effect. Eclipsing of hydrogen atoms is an important destabilizing effect, as well. The strain energy of a cycloalkane is the theoretical increase in energy caused by the compound's geometry, and is calculated by comparing the experimental standard enthalpy change of combustion of the cycloalkane with the value calculated using average bond energies.

Ring strain is highest for cyclopropane, in which the carbon atoms form a triangle and therefore have 60 degree C-C-C bond angles. There are also three pairs of eclipsed hydrogens. The ring strain is calculated to be around 120 kJ/mol.

Cyclobutane has the carbon atoms in a puckered square with approximately 90-degree bond angles; "puckering" reduces the eclipsing interactions between hydrogen atoms. Its ring strain is therefore slightly less, at around 110 kJ/mol.

For a theoretical planar cyclopentane the C-C-C bond angles would be 108 degrees, very close to the measure of the tetrahedral angle. Actual cyclopentane molecules are puckered, but this changes only the bond angles slightly so that angle strain is relatively small. The eclipsing interactions are also reduced, leaving a ring strain of about 25 kJ/mol.

In cyclohexane the ring strain and eclipsing interactions are negligible because the puckering of the ring allows ideal tetrahedral bond angles to be achieved. As well, in the most stable chair form of cyclohexane, axial hydrogens on adjacent carbon atoms are pointed in opposite directions, virtually eliminating eclipsing strain.

After cyclohexane, the molecules are unable to take a structure with no ring strain, resulting in an increase in strain energy, which peaks at 9 carbons (around 50 kJ/mol). After that, strain energy slowly decreases until 12 carbon atoms, where it drops significantly; at 14, another significant drop occurs and the strain is on a level comparable with 10 kJ/mol. After 14 carbon atoms, sources disagree on what happens to ring strain, some indicating that it increases steadily, others saying that it disappears entirely.

Reactions

The simple and the bigger cycloalkanes are very stable, like alkanes, and their reactions, for example, radical chain reactions, are like alkanes.

The small cycloalkanes - particularly cyclopropane - have a lower stability due to Baeyer strain and ring strain. They react similarly to alkenes, though they do not react in electrophilic addition, but in nucleophilic aliphatic substitution. These reactions are ring-opening reactions or ring-cleavage reactions of alkyl cycloalkanes. Cycloalkanes can be formed in a Diels-Alder reaction followed by a catalytic hydrogenation.

References

External links

• "Cycloalkanes" at the online Encyclopædia Britannica
• "Cycloalkanes" by the Chemistry staff at Westminster College