Propene is more reactive towards \(\text{Br}_2\) (gaseous) than \(\text{CH}_2=\text{CH}_2\) (ethylene), \(\text{HC} = \text{CH}\) (acetylene), and butane. This is due to the greater electron density in propene.
In the case of alkene reactions with bromine, the reactivity depends on the availability of electron density for the electrophilic addition reaction. In the case of propene:
Propene is the most reactive towards gaseous bromine because the electron density around the double bond is higher compared to the other molecules, facilitating a faster electrophilic addition reaction.
An alkene X (\( C_4H_8 \)) on reaction with HBr gave Y (\( C_4H_9Br \)). Reaction of Y with benzene in the presence of anhydrous \( AlCl_3 \) gave Z which is resistant to oxidation with \( KMnO_4 + KOH \). What are X, Y, Z respectively?
Which of the following alkenes is most stable?
Identify the major product C formed in the following reaction sequence:
In organic chemistry, an alkene is a hydrocarbon containing a carbon-carbon double bond.[1]
Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.
Read More: Ozonolysis
Read More: Unsaturated Hydrocarbon