alkene

The pendant group could be chosen from a number of alkene functionalized systems.

The content of hydrocarbons (mainly alkenes and aromatics) and also oxygenates (methyl tert-butyl ether, ethanol, etc.) in petrol determines the type and amount of additives to be used.

All chromatograms are dominated by alkanes and alkenes with 8-32 carbon atoms, and the peak from each n-alkane is accompanied by a peak from the corresponding n-alkene.

Ma, "Epoxidation of alkenes efficiently catalyzed by Mo salen supported on surface-modified halloysite nanotubes," Chinese Journal of Catalysis, vol.

The in situ produced peroxy acid then oxidises the alkene, affording the respective epoxide and regenerating the carboxylic acid.

Statistical parameters were also calculated for total alkanes [C.sub.2]-[C.sub.5] and total alkenes [C.sub.2]-[C.sub.4] as well as for geochemical ratios [C.sub.1]/[SIGMA]([C.sub.2]-[C.sub.5]), [C.sub.2][H.sub.6]/[C.sub.3][H.sub.8] ([C.sub.2]/[C.sub.3]), and [C.sub.2][H.sub.6]/[C.sub.2][H.sub.4] ([C.sub.2]/[C.sub.2=]).

Patent 9,617,354 (April 11, 2017), "Electro-initiated Poly of Compositions Having a 1,1-Disubstituted Alkene Compound," Peter Rulon Stevenson and Jeffrey M.

In this system, II free radical attacked the [beta]-carbon of V free radical to generate VII free radical and alkyl radical with molecular weight of 141, whereas alkyl radical lost H atom and formed the alkene with molecular weight of 140 (Scheme 1(j and k)).

Category Main components Aromatic hydrocarbons Ethylbenzene, 1,3-dimethyl benzene, 1-methylene lH-indene, butylated hydroxy toluene, 1-methylnaphthalene, 2-methylnaphthalene Alkanes Undecane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, 2,6,10-trimethyl dodecyl, 4-(prop-2 loxypropangl)octane, 2,6-dimethyl decane Alkenes 2-Propenylidene cyclobutene, cedrene, Seychelles alkene Aldehydes and ketones Hexanal, nonanal, benzaldehyde, acetophenone, undecanal Esters Butyl butyrate, 3-methyl heptanol acetate, 2 acrylic acid 2 ethylhexyl ester, oxalic acid acrylate Others TV-butyl ether

Regarding alkyne hydrogenation, the major aim is to avoid hydrogenation to single bond and in the case of non-terminal alkynes is to give superiority to the extreme conversion and selectivity to the (Z)- alkene [3-5].

In addition, the student used alkene, the low-price and eco-friendly substance, as a prefix substance for interaction rather than the epoxide expensive substance, which is typically used to prepare Cyclic Carbonate through a nano-meter industrial catalytic.

If only the alkyne carboalumination could be modified for discovering the corresponding alkene carboalumination reaction with suitable chiral zirconocene derivatives, we would most likely discover a catalytic and enantioselective C--C bond-forming reaction, namely the ZACA (Zr-catalyzed asymmetric carboalumination of alkenes).

Therefore, we report herein the modification process of the epoxy resin with compounds having epoxide, ester and alkene groups and how the modification process affects mechanical properties of the epoxy resin.