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Why Was Br2 Dissolved In Cyclohexane And Not In Water


Why Was Br2 Dissolved In Cyclohexane And Not In Water. Exactly which frequencies molecules absorb depends on the arrangement of electrons. Bromine (br2) breaks this c=c double bond and attaches itself to the alkene.

Solved Reaction Of Bromine With Hydrocarbons Reactivity O...
Solved Reaction Of Bromine With Hydrocarbons Reactivity O... from www.chegg.com

It's not just cyclohexene, but all alkene molecules that decolourise when they react with bromine water. The secondary alcohol cyclohexanol is oxidized by permanganate to give the ketone cyclohexanone. Therefore, it shows that cyclohexene is more reactive than cyclohexane.

For Cyclohexane, Say That Bromine Water Did Not Colourise In The Abscence Of Uv Light And Remained Yellow Before And After Shaking.


Which hydrocarbon reacted immediately with the bromine (did. Therefore, no reaction has occurred. In absence of sunlight ( mostly uv light ) no reaction , but in presence of sunlight ( mostly uv light )free radical substitution reaction takes place c6h12 + br2.

Backside Attack Of Bromide On The Positively Charged Bromonium Ion Means That The Resulting.


Why br2 is not soluble in water? Why was br2 dissolved in cyclohexane and not in water? Why is cyclohexane not soluble in water?

You're Welcome, Although You Don't Get Bromocyclohexane Because It Doesn't React With Bromine, It Only Dissolves In The Layer.


Alkenes contain a c=c double bond and thus we call them unsaturated hydrocarbons. The top layer is cyclohexane and the bottom layer is water. The permanganate ion is reduced to the green manganate ion.

Since Hydrocarbons Are Non Por And Water Polar It's Not Going To


The secondary alcohol cyclohexanol is oxidized by permanganate to give the ketone cyclohexanone. Why does cyclohexane not react with bromine? Why was br2 dissolved in cyclohexane and not in water?

You Must Mention The Sentence In Bold Because Thats What The Experiment Is About.


Bromine is more soluble in hexane than water. Therefore, it shows that cyclohexene is more reactive than cyclohexane. Exactly which frequencies molecules absorb depends on the arrangement of electrons.


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