Draw the product you expect from the reaction of (R)-2-bromooctane with -CN. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it.

See explanation and image attached

Explanation:

The reaction between (R)-2-bromooctane and -CN^- is an SN2 reaction. An SN2 reaction involves a synchronous attack of the nucleophile as the leaving group is departing.

This leads to a five member transition state in which a bond is being broken and another is being made. Since the nucleophile attacks from the backside, SN2 mechanism leads to inversion of configuration as shown in the image attached.

it should be all of them because it asks if you included all of those in your answer

explanation:

< > according to newton's third law of motion, forces always act in equal but opposite pairs. another way of saying this is for every action, there is an equal but opposite reaction.< >