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The Bromine test for alkenes works because bromine is electron deficient and alkenes have pi electrons forming a double bond that are open for attack.

The exact mechanism is shown here:
http://en.wikipedia.org/wiki/Halogen_addition_reaction

Alkanes can be brominated but the reaction is a lot slower and it requires a UV light catalyst (it's a radical bromination)

2006-11-04 15:54:52 · answer #1 · answered by niuchemist 6 · 0 0

The reaction is:

H2C=CH2 + Br2 ---> BrH2C-CH2Br

Due to their C=C double bonds which can be broken, alkenes react readily with bromine to produce saturated dibromoalkanes. When an alkene is reacted with bromine, the red-brown color of the bromine is immediately lost due to the reaction of the bromine.

2006-11-04 10:05:55 · answer #2 · answered by Dr. J. 6 · 0 0

an alkene has 1 or more double bonds between carbon atoms C=C. in the presence of Br2 or Br-Br( which is red/brown), the Br-Br bond attacks the double bond forming C-Br new bonds. thus the red/brown colour dissappears. Alkanes do not have C=C, but have C-C which Br-Br can not attach to.

2006-11-04 10:08:26 · answer #3 · answered by toasteddeer 2 · 1 0

triple bond.

2016-03-17 06:24:47 · answer #4 · answered by ? 4 · 0 0

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