Cycloalkanes (also called naphthenes) are chemicals with one or more hydrogen rings to which carbon atoms are attached according to the formula CnH2n. 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.
- 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 (eg, "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 which consists of a six-member ring and a four member ring, which share two adjacent carbon atoms which 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.
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 only containing unreactive C-C and C-H bonds; however, the ring strain (see below) can cause cycloalkanes to be more reactive.
The carbon atoms in cycloalkanes are sp3 hybridized and therefore a deviation from the ideal tetrahedral bond angles of 109.47 degrees 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; by "puckering" it reduces the eclipsing interactions between hydrogen atoms. Its ring strain is 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 tetrahedral angle. Actual cyclopentane molecules are puckered but this only changes 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.
The small cycloalkanes - particularly cyclopropane - have a lower stability due to Baeyer strain and ring strain. They react similarly to alkenes, though they don't 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.
- "Cycloalkanes" at the online Encyclopædia Britannica
- "Cycloalkanes" by the Chemistry staff at Westminster Collegede:Cycloalkane
There is no pharmaceutical or device industry support for this site and we need your viewer supported Donations | Editorial Board | Governance | Licensing | Disclaimers | Avoid Plagiarism | Policies