Be sure to answer all parts. Show the overall reaction for formation of racemic 3−bromohexane from (E)−3−hexene by entering the structures of the products and reactants in the template provided. Part 1 out of 3 draw structure ... arr draw structure ... + draw structure ... (E)−3−hexene (S)−3−bromohexane (R)−3−bromohexane Racemic product = 50% (S) and 50% (R)

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.

he uptake of drugs from the intestine is often strongly influenced by diffusion. for example, consider a water-insoluble steroid for treating inflammation that is solubilized in aggregates of detergent molecules, called micelles. these micelles, aggregates of 80 soap molecules, have a molecular weight of 24,000, a diameter of 2.6 nm, and a charge of -27. the positively charge ions (counterions) in this system are na".