Answer:
Use the Bromotriflouride catalyst, BF₃
Explanation:
The BF₃ is most likely to yield less desired side products. The effect lies in the reaction mechanism.
BF₃ is a Lewis acid. Its role is to promote the ionization of the HF. This is achieved through the electrophilic mechanism. The reaction mechanism is as follows:
2 - methylpropene + H-F-BF₃ → H-F + H₃C + benzene
butylbenzene + F-BF₃ → tert-butylbenzene + H-F + BF₃ (regenerated catalyst)
Answer:
10g/cm^3, I think.
Explanation:
2x2x2=8cm^3 for the volume.
Divide 80g by that, you get 10g/cm^3, I think.
The longest hydrocarbon chain in the given compound is hexane, therefore it is the parent chain to be considered with one methyl group attached to the 3rd carbon and one chloro attached on the 2nd carbon, therefore the name of the compound is 2-chloro-3-methylhexane
If its sodium it would have 11 electrons