What is the Difference Between Alcoholic KOH and Aqueous KOH?
🆚 Go to Comparative Table 🆚The main difference between alcoholic KOH and aqueous KOH lies in the solvent used to dissolve the potassium hydroxide (KOH) and the resulting ions present in each solution.
- Alcoholic KOH: This is potassium ethoxide, with the chemical formula C2H5OK. When it dissociates in water, it gives C2H5O– ions and K+ ions. The C2H5O– ions act as strong bases and can replace a hydrogen atom from an alkyl halide. Alcoholic KOH solutions prefer to undergo elimination reactions.
- Aqueous KOH: This is potassium hydroxide in water. It consists of KOH dissolved in water, forming K+ ions and OH– ions. Aqueous KOH is more solvated by water and acts as a stronger nucleophile, preferred for substitution reactions.
In summary, the key difference between alcoholic KOH and aqueous KOH is that alcoholic KOH forms C2H5O– ions and is more likely to undergo elimination reactions, while aqueous KOH forms OH– ions and is more likely to undergo substitution reactions.
Comparative Table: Alcoholic KOH vs Aqueous KOH
The main difference between alcoholic KOH and aqueous KOH lies in their structure and reactivity. Here is a comparison table highlighting the differences:
Feature | Alcoholic KOH | Aqueous KOH |
---|---|---|
Chemical Formula | C2H5OK | KOH |
Ions Formed | C2H5O^(-) and K^+ | OH^- and K^+ |
Reaction Preference | Elimination reactions | Substitution reactions |
Basicity | Strong base due to the presence of C2H5O^(-) ions | Weaker base compared to alcoholic KOH |
Alcoholic KOH is potassium ethoxide, and when it dissociates in water, it forms C2H5O^(-) ions and K^+ ions. Aqueous KOH, on the other hand, is potassium hydroxide in water and dissociates into OH^(-) and K^+ ions. Alcoholic KOH prefers to undergo elimination reactions, while aqueous KOH prefers substitution reactions. The higher basicity of alcoholic KOH compared to aqueous KOH is due to the presence of C2H5O^(-) ions, which are more basic than OH^(-) ions.
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