Organic chemistry problem??
Compounds X has the formula C7H15Cl; Y is C7H15Br.
X undergoes base-promoted E2 elimination to give a single alkene product Z. Y likewise reacts under similar conditions to give a single alkene product that is isomeric with Z
Catalytic hydrogenation of Z affords 3-ethylpentane.
X readily reacts in SN2 fashion with sodium iodide in acetone. Y does not undergo a similar SN2 reaction. Propose structures for X and Y.