

Answer: A (made by addition polymerisation of the monomer with a C=C double bond). The polymer has a repeating unit in which two carbon atoms each carry a hydrogen and a CH₂Cl group, a saturated chain with no double bonds along the backbone.
Such a chain is formed by addition polymerisation: the monomer is an alkene, CH(CH₂Cl)=CH(CH₂Cl), whose C=C double bond opens up so that many monomers join head-to-tail into a long saturated chain with no small molecule lost. That makes statement A correct.
Condensation polymerisation (B) is wrong because it needs monomers with two functional groups that eliminate a small molecule such as water; an alkene undergoes addition, not condensation. The claim about the empirical formula (C) is wrong because the simplest ratio of the repeat unit C₄H₆Cl₂ is actually C₂H₃Cl. And making the monomer by reacting an alkane with chlorine (D) is wrong because that gives a chloroalkane by substitution, with no C=C double bond to polymerise. So the answer is A.
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