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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» <html><body><p></p><a href="https://interviewquestions.tuteehub.com/tag/solution-25781" style="font-weight:bold;" target="_blank" title="Click to know more about SOLUTION">SOLUTION</a> :`2CH_(<a href="https://interviewquestions.tuteehub.com/tag/3-301577" style="font-weight:bold;" target="_blank" title="Click to know more about 3">3</a>)CH_(2)Br+Ag_(2)O <a href="https://interviewquestions.tuteehub.com/tag/overset-2905731" style="font-weight:bold;" target="_blank" title="Click to know more about OVERSET">OVERSET</a>("Heat")to CH_(3)CH_(2)OCH_(2)CH_(3)+2AgBr`</body></html> | |