Definition of Alkenes. Meaning of Alkenes. Synonyms of Alkenes

Here you will find one or more explanations in English for the word Alkenes. Also in the bottom left of the page several parts of wikipedia pages related to the word Alkenes and, of course, Alkenes synonyms and on the right images related to the word Alkenes.

Definition of Alkenes

No result for Alkenes. Showing similar results...

Meaning of Alkenes from wikipedia

- ****ulenes. Alkenes having four or more carbon atoms can form diverse structural isomers. Most alkenes are also isomers of cycloalkanes. Acyclic alkene structural...
- organic chemistry, terminal alkenes (alpha-olefins, α-olefins, or 1-alkenes) are a family of organic compounds which are alkenes (also known as olefins) with...
- temperature. Thus, trans alkenes, which are less polar and more symmetrical, have lower boiling points and higher melting points, and cis alkenes, which are generally...
- four-component system central to the bacterial metabolism of aliphatic alkenes". J. Biol. Chem. 272 (40): 24913–20. doi:10.1074/jbc.272.40.24913. PMID 9312093...
- engines for their higher octane rating. Trans-alkenes are about 1 kcal/mol more stable than cis-alkenes. An example of this effect is cis- vs trans-2-butene...
- bonds between carbon atoms. Those with one or more double bonds are called alkenes. Those with one double bond have the formula CnH2n (****uming non-cyclic...
- ligands. Ziegler–Natta catalysts are used to polymerize terminal alkenes (ethylene and alkenes with the vinyl double bond): n CH2=CHR → −[CH2−CHR]n−; The 1963...
- metal catalyzed reactions of alkenes: polymerization., hydrogenation, hydroformylation, and many other reactions. Since alkenes are mainly produced as mixtures...
- photochemical [2+2] cycloaddition is allowed, the reaction between enones and alkenes is stepwise and involves discrete diradical intermediates. In 1908, it...
- synthesis of N-aryl pyrrolidines from γ-(N-arylamino) alkenes: evidence for chemoselective alkene insertion into Pd–N bonds". Angew. Chem. Int. Ed. 43...