Cycloalkene

Source: Wikipedia, the free encyclopedia.

In

bridged
ring systems because the alkene would necessarily be trans in one of the rings.

Examples

Nomenclature

Cycloalkenes follow a similar nomenclature system to alkenes, but the carbons are numbered starting at a carbon on the double bond and then through the double bond and around the ring.[3] This method is used to keep the index numbers small.

  • 1-methylcyclohexene
    1-methylcyclohexene
  • 3-methylcyclohexene
    3-methylcyclohexene

Properties

Cycloalkenes with a small ring have about 20° more bond angle strain than a cycloalkane of the same size.[4] This is because the bond angle for an alkene, C-C=C, is 122°, while the bond angle for an alkane, C-C-C, is 112°. When these carbons form a small ring, the alkene which has a larger bond angle will have to compress more than the alkane causing more bond angle strain.[4]

Cycloalkenes have a lower melting point than cycloalkanes of the same size. The lowered melting point is due to the double bond preventing the compound from compact packing.

Cycloalkenes generally reflect physical properties of their cycloalkane. In physical states, only the smaller cycloalkenes are gases while the others are mostly liquid. These molecules are also more reactive than cycloalkanes due to increased electron density shifts of the double bond. [5]

Trans isomers

As previously mentioned, cis-isomers of cycloalkenes exhibit more stability than trans-isomers; however, on an experimental and computational level, this property is only applicable to cycloalkenes with 10 carbons or less. As the number of carbons increase, the possibility of a trans-isomer occurring also increase.[6] The geometrical considerations as analyzed by computational analysis are as follows.

The most stable trans-isomers of 10 ring or greater cycloalkenes exhibit 4  irregularities from standard geometric norms. The first irregularity is twisted planes of substituents along the C=C. Using C=C as the stable axis, 2 substituents of 1 carbon can be visualized on the same plane, equally applied to the other carbon. These planes are not planar and instead one carbon substituent plane twists along the axis away or toward the other carbon’s plane. This twisting leads to pyramidalization forming a

Pyramidalization is important in highered number rings, because it increases p-orbital overlap for stability, and reduces torsional strain. [7]

Bond length between the C=C and corresponding vinylic carbons also vary. In smaller cycloalkenes, it is expected for the bonds to be greater in length uniformly to account for increased strain, but for example, trans-cycloheptane has varying bond lengths. Also, the vinylic carbons on trans cyclohexanes exhibit longer bond lengths than their respective cis isomer for trans-cycloheptane through trans-cyclononene (7 carbon and 9 carbon cycloalkenes).[8]

Synthesis reactions

Ring-closing metathesis

Ring-closing metathesis switches out functional groups from one or multiple terminal alkenes to form a cycloalkene.[9] This process can be used to form cycloalkenes of either E or Z configurations, depending on the stereochemistry of the second ring strain.[10]

Formation of a cycloalkane via ring closing metathesis
Formation of a cycloalkane via ring closing metathesis

Birch reduction

Birch reduction is a possible method to reduce reduces aromatic compounds into cycloalkenes, specifically cyclohexadiene.[11]

Formation of a cycloalkane via Birch Reduction
Formation of a cycloalkane via Birch Reduction

Diels-Alder reaction

The

Diels-Alder reaction, also known as cycloaddition, combines a conjugated diene and an alkene to form cycloalkene. This is a concerted process, with bonds forming and breaking simultaneously.[11]

Formation of a cycloalkane via a Diels-Alder Reaction
Formation of a cycloalkane via a Diels-Alder Reaction

Cyclization reactions

Cyclization reactions, or intramolecular addition reactions, can be used to form cycloalkenes. These reactions primarily form cyclopentenones, a cycloalkene that contains two functional groups: the cyclopentene and a ketone group.[12] However, other cycloalkenes, such as Cyclooctatetraene, can be formed as a result of this reaction.[11]

Formation of a cyclohexane from a non-cyclic compound via a Cyclization Reaction
Formation of a cyclohexane from a non-cyclic compound via a Cyclization Reaction

Electrocyclic reactions

Reactions of conjugated double-bond systems can be synthesized into cycloalkenes through electrocyclic reactions.[13] Addition of heat or photolysis causes a reversible reaction that causes one pi bond to become a sigma bond, which closes the ring and creates a cycloalkene.[11]

Formation of a cycloalkane via an electrocyclic reaction
Formation of a cycloalkane via an electrocyclic reaction

Intramolecular McMurry reactions

When two carbonyl groups are coupled and undergo a McMurry reaction, there is a possibility of the formation of cycloalkenes under specific conditions.[11] When both carbonyls are within the same molecule and not sufficiently separated from each other, a cycloalkene can be formed through an intramolecular McMurry reaction.[11]

Formation of a cycloalkane via an Intramolecular McMurry Reaction

See also

References

  1. PMID 30271676
    .
  2. ISBN 978-0-12-800780-8
    , retrieved 2022-11-17
  3. ^ "3.4: Alkenes, Cycloalkenes, and Alkadienes". Chemistry LibreTexts. 2014-11-26. Retrieved 2021-03-20.
  4. ^ a b "12.7: Cycloalkenes and Cycloalkanes". Chemistry LibreTexts. 2014-11-22. Retrieved 2021-03-20.
  5. ^ "Cycloalkenes". Organic Chemistry. Retrieved 2022-11-17.
  6. ISBN 978-0-12-800780-8
    , retrieved 2022-11-17
  7. ISBN 978-0-12-800780-8
    , retrieved 2022-11-17
  8. ISBN 978-0-12-800780-8
    , retrieved 2022-11-17
  9. ^ "Ring Closing Metathesis - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2022-11-17.
  10. ^ "Olefin Metathesis". Chemistry LibreTexts. 2016-12-17. Retrieved 2022-11-17.
  11. ^ a b c d e f "Cycloalkenes - Chemgapedia". www.chemgapedia.de. Retrieved 2022-11-17.
  12. ^ "III. Intramolecular Addition (Cyclization) Reactions". Chemistry LibreTexts. 2015-01-12. Retrieved 2022-11-17.
  13. ^ "ELECTROCYCLIC REACTIONS". research.cm.utexas.edu. Retrieved 2022-11-17.
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