S_N1 The Leaving Group

We said during the discussion of S_N2 reactivity that the best leaving groups are those that are most stable; that is, those that are the conjugate bases of strong acids. An identical reactivity order is found for the SN1 reaction because the leaving group is directly involved in the rate-limiting step. Thus, the S_N1 reactivity order is

Note that in the S_N1 reaction, which is often carried out under acidic conditions, neutral water is sometimes the leaving group. This occurs, for example, when an alkyl halide is prepared from a tertiary alcohol by reaction with HBr or HCl. As shown in Figure 11-13, the alcohol is first protonated and then spontaneously loses H₂O to generate a carbocation, which reacts with halide ion to give the alkyl halide. Knowing that an S_N1 reaction is involved in the conversion of alcohols to alkyl halides explains why the reaction works well only for tertiary alcohols. Tertiary alcohols react fastest because they give the most stable carbocation intermediates.

Figure 11-13: The mechanism of the SN1 reaction of a tertiary alcohol with HBr to yield an alkyl halide. Neutral water is the leaving group (step 2 ).

مواضيع ذات صلة

مركبات الآزو متجانسة الحلقة Homocyclic azo compounds

تصنيف مركبات الآزو Classification of azo compound

أصباغ الآزو Azo Dye

تفاعلات الازدواج Reaction Coupling

أملاح الدايازونيوم الاروماتية      Aromtic Diazonium Salt    

أهمية الكواشف العضوية reagents Importance of organic

الثايوزبينات Thiazepines

الدايازبينات Diazepines

الاوكسازبينات Oxazepines

المركبات الحلقية غير المتجانسة Heterocyclic Compounds

نبذة عن مظاهر كيمياء الكلورامين-T الحيوية واهميته

بعض مظاهر كيمياء الكلورامين-T