Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-), etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2. S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Complete the reaction: CH_(3)CH_(2)Br underset("Heat")overset(Ag_(2)O)to

Alkylhalides have polar C-X bond and undergo nucleophilic substitution

1.	Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-), etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2. S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Complete the reaction: CH_(3)CH_(2)Br underset("Heat")overset(Ag_(2)O)to
Answer» SOLUTION :`2CH_(3)CH_(2)Br+Ag_(2)O OVERSET("Heat")to CH_(3)CH_(2)OCH_(2)CH_(3)+2AgBr`