Construct a mechanism for the light-initiated reaction of cyclohexane with chlorine to give chlorocyclohexane. Cyclohexane reacts with chlorine gas in the presence of light to produce chlorocyclohexane and hydrochloric acid. The ring CH2CH2CH2CH2CH2CH2 plus CH2 react in the presence of hv to form the substituted ring CH(Cl)CH2CH2CH2CH2CH2 plus HCl. Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. Include all free radicals by right-clicking on an atom on the canvas and then using the Atom properties to select the monovalent radical.

For cyclohexane compounds drawn in a chair conformation:   -axial bonds are vertical  -equatorial bonds are parallel to two bonds within the ring.  thus, as i assume the chair conformation is drawn:   -the x group is in an axial position, as are the five other vertical bonds.  -three axial bonds are on the top face of the ring  -the other three axial bonds are on the bottom face  the position of the second substituent on each ring carbon is equatorial.  gauche groups must be on an adjacent carbon such as carbon 6 and carbon 2, and also gauche groups are rotated by 60 degrees relative to each other.  drawing the newman projections for c1–c2 and c1–c6 aids in visualizing the groups that are gauche to the y group on c1.  click this link and watch some academic videos that may you more understand the topic 

The answer is c) pyrite

The answer to this qustion is c