Bromination occurs on alkene functional groups, but NOT on alkenes found within aromatic functional group, such as the phenyl ri
ng of cinnamic acid. Chemists would describe this difference in reactivity as an example of _____
1 answer:
Answer:
When cinnamic acid react with bromine ,addition reaction rapidly occur on alkene functional group to form dibromo product
Explanation:
Phenyl ring is an aromatic hydrocarbon ,when aromatic hydrocarbons react with Cl2,Br2 or KMnO4 no reaction occur ,where as unsaturated hydrocarbon like alkene react .Aromatic hydrocarbon with these reagents undenr different conditions undergoes subtituition reaction.They react with bromine in presence of lewis acid catalyst ferric bromide.
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Answer:
Explanation:
Hello!
In this case, since the reaction may be assumed in chemical equilibrium, we can write up the rate law as shown below:
However, since the rate of reaction at equilibrium is zero, due to the fact that the concentrations remains the same, we can write:
Which can be also written as:
Then, we solve for the concentration of NO to obtain:
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Delta energy on labelled diagram is attached below
