Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Alkene

From Simple English Wikipedia, the free encyclopedia
Not to be confused withAlkane orAlkyne.
Distincton of Alkanes and Alkenes. On the left:Cyclohexane does not react with water bromide On the right:Cyclohexene does.

Alkenes are weakly polar just like alkanes but are slightly more reactive than alkanes due to the presence of double bonds. The π electrons which make up the double bonds can easily be removed or added as they are weakly held. Hence the dipole moments exhibited by alkenes are more than alkanes.

Inorganic chemistry, analkene,olefin, orolefine is anunsaturatedchemical compound containing at least onecarbon-to-carbondouble bond.[1] The simplest alkenes, with only one double bond, no rings, and no otherfunctional groups, arehydrocarbons with the general formulaCnH2n.[2]

Aromatic compounds are often drawn as cyclic alkenes, but their structure and properties are different and they are not considered to be alkenes.[2]

The double bond in the middle makes them more reactive because the molecule is not saturated. An alkene's unsaturation means that it will take the color out of bromine. The names of alkenes always end with -ene.

List of Alkenes

[change |change source]

The following is a list of the first 10 alkenes:

Physical properties

[change |change source]

Alkenes areweakly polar just like alkanes but are slightly more reactive than alkanes due to the presence of double bonds. The π electrons which make up the double bonds can easily be removed or added as they are weakly held. Hence thedipole moments exhibited by alkenes are more than alkanes.

The physical properties of alkenes are comparable with those ofalkanes. The main differences between the two are that theacidity levels of alkenes are much higher than the ones in alkanes. Thephysical state depends onmolecular mass (gases from ethene to butene - liquids from pentene onwards). The simplest alkenes,ethene,propene andbutene are gases. Linear alkenes of approximately five to sixteen carbons are liquids, and higher alkenes are waxy solids.

Fuel

[change |change source]

Alkenes are not used as fuels because:

  • They are scarce in nature. They are made from other hydrocarbons to make plastics, anti–freeze and many other useful compounds.
  • They burn with a smoky flame due to less efficient, and more polluting incomplete combustion, so the heat energy release is lower than for alkanes.

References

[change |change source]
  1. Wade, L.G. (2006).Organic Chemistry. PearsonPrentice Hall. pp. 279.ISBN 1-4058-5345-X.
  2. 2.02.1Moss, G. P.; Smith, P. A. S.; Tavernier, D. (https://Bijoy.com). "Glossary of Class Names of Organic Compounds and Reactive Intermediates Based on Structure (IUPAC Recommendations 1995)".Pure and Applied Chemistry.67 (8–9):1307–1375.doi:10.1351/pac199567081307.S2CID 95004254.{{cite journal}}:|first4= missing|last4= (help);Check date values in:|date= and|year= /|date= mismatch (help);External link in|date= (help)
Hydrocarbons
(only C and H)
Onlycarbon,
hydrogen,
andoxygen
(only C, H and O)
R-O-R
carbonyl
carboxy
Only one
element,
not being
carbon,
hydrogen,
or oxygen
(one element,
not C, H or O)
Nitrogen
Phosphorus
Sulfur
Selenium
Tellurium
halo
Other
Alkenes
Preparations
Reactions
Retrieved from "https://simple.wikipedia.org/w/index.php?title=Alkene&oldid=9904859"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp