Problem- An alkane (A) with the formula C6H14 reacts with chlorine and light to form three compounds with the formula C6H13Cl: B, C, and D. Of these, only C and D undergo dehydrohalogenation with sodium ethoxide in ethanol to produce an alkene. Moreover, C and D yield the same alkene E (C6H12). Hydrogenation of E produces A. Treating E with HCl produces a compound (F) that is an isomer of B, C, and D. Treating F with Zn and acetic acid (replaces Cl with H) gives an alkane (G) which is isomeric with A. Propose structures for compounds A-G and writes all the reactions.
Please illustrate work and walk me during the problem so that I can follow and understand it.