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Electrophilic addition. Forms 1,2,-dibromocyclohexane
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No. When bromine (aq) reacts with cyclohexene, the compound is now saturated, and will no longer have C=C bonds, thus it is unable to exhibit cis-trans isomerism.
Halogens react with alkenes to form haloalkanes. Addition of the bromine in this case occurs across the double bond in cyclohexene. The resultant products are colourless hence the brown colour disappears.
2KCl + Br2 ---> Cl2 + 2KBr
Bromine dissapear in this reaction !
Electrophilic addition. Forms 1,2,-dibromocyclohexane
Cyclohexene picks up the bromine from solution and becomes dibromoethylcyclohexane.
Any reaction occur between neon and bromine.
The chemical equation is:C2H4 + Br2 = C2H4Br2
The chemical reaction is:C2H2 + Br2 = CHBr=CHBr
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Bromine attacks triolein at three places where double bonds exist in the structure, causing saturated molecule. The equation for the reaction of triolein with bromine is C57 H104 06 + 3 Br2 --> C57 H104 06 Br6.
The chemical equation is:C2H2 + 2 Br2 = C2Br2H4
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No. When bromine (aq) reacts with cyclohexene, the compound is now saturated, and will no longer have C=C bonds, thus it is unable to exhibit cis-trans isomerism.
Halogens react with alkenes to form haloalkanes. Addition of the bromine in this case occurs across the double bond in cyclohexene. The resultant products are colourless hence the brown colour disappears.