Answer:
See explanation
Explanation:
The mechanism for the formation of bromohexane from hexene has been clearly shown in the image attached to this answer.
Hexene is attacked by HBr and a carbocation is first formed as shown. The carbocation is flat and planar. it can be attacked on either face by the bromide ion.
Attack on either faces yields a racemic mixture of the R and S enantiomer as shown in the image.
You can use the mechanism shown to fill in the structures.
first you divide them together and get an answer of 10 then you times it by 5 and your answer is 50 ml