Examples of 'cyclohexene' in a sentence
Meaning of "cyclohexene"
cyclohexene (noun): A type of organic compound belonging to the cycloalkene group, commonly used in the production of plastics, resins, and solvents
Show more definitions
- A cyclic hydrocarbon containing six carbon atoms and one double bond; any of its derivatives.
How to use "cyclohexene" in a sentence
Basic
Advanced
cyclohexene
Cyclohexene has been studied extensively by analytical methods.
It will no longer be cyclohexene oxide exactly.
The cyclohexene oxide is also hydrogenated to cyclohexanol.
The hydrogen source may be cyclohexene or ammonium formate.
Cyclohexene oxide is produced in epoxidation reaction from cyclohexene.
Penoxypronpionic herbicide cyclohexene oxime herbicide dinitroanaline herbicide.
Cyclohexene usually can not be homopolymerised by olefin metathesis.
The preferred stabilization agents are the derivatives of cyclohexene.
Cyclohexene was the major initial product.
Alternative hydrogen sources include ammonium formate or cyclohexene.
The formation of a cyclohexene byproduct was detected in some formulas.
Examples of cycloolefins are cyclopentene and cyclohexene.
The oxidation of cyclohexene by ceric ammonium nitrate has been studied.
Below is shown the dimerisation of cyclohexene.
Wide variety of cyclohexene compounds may be used as stabilization agents.
See also
Examples of cycloalkenes are cyclohexene and norbornene.
Heating in the presence of acid catalysts converts cyclohexanol to cyclohexene.
Cyclohexene oxime herbicide.
Under these conditions all vinyl cyclohexene was converted.
Cyclohexene oxime herbicides.
It can also be oxidized to cyclohexene.
These contain the trimethyl cyclohexene ring system present in retinol.
Examples of the hydrogen source include hydrogen and cyclohexene.
The dehydrogenation of cyclohexane to cyclohexene can be effected in any known manner.
The cyclohexene can be removed by any convenient method such as described hereinabove.
Preferred are cyclopentene and cyclohexene.
This hydration of cyclohexene to cyclohexanol can be carried out in any known manner.
Examples of suitable monocyclic monomers include cyclohexene and cyclopentene.
Examples thereof include cyclohexene anhydride and adducts with furan or cyclopentadiene.
Two hydrocarbons that can serve as hydrogen donors are cyclohexene or cyclohexadiene.
The remaining diethyl ether and cyclohexene oxide were removed by partial vacuum distillation.
An example is cyclohexenyl or cyclohexene.
Trianhydrides such as the benzene and cyclohexene hexacarboxylic acid trianhydrides are also useful.
Examples of partially saturated cycloalkyl groups include cyclohexene and indane.
Equal molar amounts of the amine and cyclohexene epoxide typically provide satisfactory results.
Similar zeolites may also be used in the selective hydrogenation of benzene to cyclohexene.
The following scheme shows the reaction of cyclohexene with mCPBA to give an epoxide.
The catalyst is suitable for use in partially reducing a monocyclic aromatic hydrocarbon to a cyclohexene.
These results indicate that a cyclohexene nucleotide can easily be accommodated in different nucleic acid structures.
A white solid was obtained for the geminal dimethyl cyclohexene aminoester intermediate.
The cyclohexene compounds may be represented by the formula,.
The optionally fused cycloalkene can be a partially unsaturated ring such as cyclopentene or cyclohexene.
The selective hydrogenation of benzene will afford cyclohexene with minor amounts of cyclohexadiene and cyclohexane.
The present invention provides for therapeutic and pharmaceutical compositions comprising cyclohexene nucleic acids.
Next, the vinyl cyclohexene diepoxide was added.
Figure 2 shows a conformational globe of puckered cyclohexene.
At the same time, cyclohexene produces benzene by direct dehydrogenation.
Examples of cycloolefins are cyclopentene, cyclohexene and norbornene.
The ring may be a cyclohexene or a cyclopentene ring, for example.
If this was just a double bond, this would be cyclohexene.