Concept:This question involves the hydrolysis of benzene diazonium chloride to phenol, followed by Williamson ether synthesis to form an allyl phenyl ether.Explanation:Step 1: Benzene diazonium chloride (C6​H5​N2+​Cl−) when warmed with water undergoes hydrolysis.The reaction produces phenol (C6​H5​OH), nitrogen gas, and hydrochloric acid.C6​H5​N2+​Cl−+H2​OΔ​C6​H5​OH+N2​+HClStep 2: Phenol is treated with sodium hydroxide to form its sodium salt, sodium phenoxide (C6​H5​ONa).C6​H5​OH+NaOH⟶C6​H5​ONa+H2​OStep 3: Sodium phenoxide reacts with allyl bromide (BrCH2​CH=CH2​) via Williamson ether synthesis.This nucleophilic substitution yields phenyl allyl ether and sodium bromide.C6​H5​ONa+BrCH2​CH=CH2​⟶C6​H5​OCH2​CH=CH2​+NaBrThus, compound [X] is phenyl allyl ether, with the structure C6​H5​−O−CH2​−CH=CH2​.Answer:Option B: C6​H5​−O−CH2​−CH=CH2​