By a proper choice of reagent, both symmetrical and unsymmetrical ethers can by prepared by williamson synthesis which involves the reaction between an alkyl halide and an alkoxide ion. The reverse process involving the cleavage of etehrs to give back the original alkyl halide and the alcohol can be carried out by heating the ether with HI at 373K. Q. Allyl phenyl ether can be prepared by heating

By a proper choice of reagent, both symmetrical and unsymmetrical ethe

1.	By a proper choice of reagent, both symmetrical and unsymmetrical ethers can by prepared by williamson synthesis which involves the reaction between an alkyl halide and an alkoxide ion. The reverse process involving the cleavage of etehrs to give back the original alkyl halide and the alcohol can be carried out by heating the ether with HI at 373K. Q. Allyl phenyl ether can be prepared by heating
Answer» `C_(6)H_(5)Br+CH_(2)=CH-CH_(2)ON a` `CH_(2)=CHCH_(2)Br+C_(6)H_(5)ON a` `C_(6)H_(5)CH=CHBr+CH_(3)ON a` `CH_(2)+CHB r+C_(6)H_(5)CH_(2)ON a` SOLUTION :`CH_(3)=CHCH_(2)Br+C_(6)H_(5)ON a UNDERSET(-NaBr)to underset("Allyl phenyl ether")(CH_(2)=CH-CH_(2)-OC_(6)H_(5))`