Search results
Results from the WOW.Com Content Network
The activation of these catalysts under H 2, produces cyclooctane, which is usually discarded or burnt: C 8 H 12 + 2 H 2 → C 8 H 16. Cyclooctane participates in no reactions except those typical of other saturated hydrocarbons, combustion and free radical halogenation. Work in 2009 on alkane functionalisation, using peroxides such as dicumyl ...
Printable version; In other projects Wikidata item; Appearance. move to sidebar hide. Solvent Density (g cm-3) Boiling point (°C) K b (°C⋅ kg/mol) Freezing point ...
1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C 8 H 8.It is also known as [8]annulene.This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature.
This organic chemistry article is a stub. You can help Wikipedia by expanding it.
Cyclooctene undergoes ring-opening metathesis polymerization to give polyoctenamers, which are marketed under the name Vestenamer. [3]cis-Cyclooctene (COE) is a substrate known for quite selectively forming the epoxide, as compared to other cycloalkenes, e.g. cyclohexene.
Main page; Contents; Current events; Random article; About Wikipedia; Contact us
trans-Cyclooctene was first synthesized on a preparatory scale by Arthur C. Cope with a Hofmann elimination reaction of N,N,N-trimethylcyclooctylammonium iodide. [10] The reaction gives a mixture of cis and trans isomers, and the trans isomer is selectively trapped as a complex with silver nitrate.
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]