




The sequence of reactions is analyzed step-by-step:
A cyclic substrate containing chlorine and bromine substituents undergoes a Wurtz reaction with sodium (Na) in diethyl ether (Et2O). This process removes two halogen atoms and forms a new carbon-carbon bond, resulting in a ring structure with two additional carbon atoms.
Intermediate compound A reacts with magnesium (Mg) in diethyl ether to generate a Grignard reagent (RMgX).
The Grignard reagent reacts with D2O, substituting the MgBr group with a deuterium atom (D) to produce compound B, a deuterated hydrocarbon.
Simultaneously, compound A reacts via a CoF2-catalyzed process to yield compound C. CoF2 acts as a catalyst, potentially indicating the formation of a fluorinated derivative or related activity.
Based on this analysis, compound B is identified as deuterated cyclopropane, and compound C is a product modified by the CoF2 catalyst. The major products B and C correspond to the structures presented in the correct answer option.

