Isopropyl chloride undergoes hydrolysis bya)SN1 mechanismb)SN2 mechani...
Secondary, primary allylic and primary benzylic halides may react predominantly either by SN1 or SN2 mechanism or by both the mechanisms without much preference, depending upon the nature of the nuclephile and the solvent.
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Isopropyl chloride undergoes hydrolysis bya)SN1 mechanismb)SN2 mechani...
SN1 and SN2 mechanism of hydrolysis of isopropyl chloride
Hydrolysis of isopropyl chloride is the reaction of isopropyl chloride with water to form isopropyl alcohol and hydrochloric acid. This reaction can occur through both SN1 and SN2 mechanisms.
SN1 mechanism
In the SN1 mechanism, the isopropyl chloride first undergoes dissociation to form a carbocation intermediate. The carbocation intermediate is then attacked by a water molecule to form isopropyl alcohol and hydrochloric acid.
The steps involved in the SN1 mechanism are:
1. Dissociation of isopropyl chloride to form a carbocation intermediate.
2. The carbocation intermediate is then attacked by a water molecule to form isopropyl alcohol and hydrochloric acid.
SN2 mechanism
In the SN2 mechanism, the hydroxide ion attacks the isopropyl chloride molecule from behind. This results in the formation of a transition state, which then leads to the formation of isopropyl alcohol and hydrochloric acid.
The steps involved in the SN2 mechanism are:
1. Attack of hydroxide ion on the isopropyl chloride molecule.
2. Formation of a transition state.
3. Formation of isopropyl alcohol and hydrochloric acid.
SN1 and SN2 mechanism
The hydrolysis of isopropyl chloride can occur through both SN1 and SN2 mechanisms because the reaction conditions can favor either mechanism. For example, in the presence of a strong nucleophile, the reaction can proceed through the SN2 mechanism, while in the presence of a weaker nucleophile, such as water, the reaction can proceed through the SN1 mechanism.
Conclusion
The hydrolysis of isopropyl chloride can occur through both SN1 and SN2 mechanisms. The mechanism that occurs depends on the reaction conditions and the strength of the nucleophile present.