Alkanes react with halogens via free radical substitution, which typically requires UV light or high heat and is slower than addition reactions.
Unsaturated hydrocarbons (Alkenes/Alkynes) react with bromine via electrophilic addition. This reaction is generally fast and characteristic of unsaturation.
Alkenes vs. Alkynes: Alkenes are generally more reactive than alkynes towards electrophilic addition reactions [NCERT 11th, Ch 13, Sec 13.4.4]. This is because the π-electron cloud in alkynes is more tightly held by the sp-hybridised carbons compared to the sp2-hybridised carbons in alkenes.
Compare Alkenes (Ethene vs. Propene):
Both Ethene (CH2=CH2) and Propene (CH3−CH=CH2) undergo electrophilic addition.
Propene contains an electron-donating methyl group (−CH3) which exerts a +I (Inductive) effect. This increases the electron density on the double bond, making it more nucleophilic and thus more reactive towards the electrophile (Br+) compared to ethene.
Therefore, Propene (C3H6) reacts most readily.
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