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In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons. In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains), and all of the carbon-carbon bonds are single.
Synthesis reactions, Properties & Ring strain
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cycloalkanes ring carbon strain atoms also rings carbons cyclopropane name example bond iupac number hydrocarbons cyclohexane chemistry form nomenclature reactions
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Cycloalkane | is a | increase in energy caused by the compound's geometry | 0.90 | text |
| bicyclic alkanes | instance of | an alkane having three carbon atoms in the main chain.The naming of polycyclic alkanes | 0.80 | text |
| spiro alkanes is more complex | instance of | an alkane having three carbon atoms in the main chain.The naming of polycyclic alkanes | 0.80 | text |
| with the base name indicating the number of carbons in the ring system | instance of | an alkane having three carbon atoms in the main chain.The naming of polycyclic alkanes | 0.80 | text |
| a prefix indicating the number of rings | instance of | an alkane having three carbon atoms in the main chain.The naming of polycyclic alkanes | 0.80 | text |
| chlorine or a methyl group | instance of | It then has room for an additional numerical prefix if there is the need to include details of other attachments to the molecule | 0.80 | text |
| Cycloalkane | related to External links | Cycloalkanes | 0.60 | section |
| Cycloalkane | related to External links | Encyclopædia Britannica | 0.60 | section |
| Cycloalkane | related to Nomenclature | Unsubstituted | 0.60 | section |
| Cycloalkane | related to Nomenclature | For | 0.60 | section |
| Cycloalkane | related to Nomenclature | C3H6 | 0.60 | section |
| Cycloalkane | related to Nomenclature | C3H8 | 0.60 | section |
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