Fischer Esterification (Ethanol + Acetic Acid)
Embed This Widget
Add the script tag and a data attribute to embed this widget.
Embed via iframe for maximum compatibility.
<iframe src="https://chemfyi.com/iframe/entity//" width="420" height="400" frameborder="0" style="border:0;border-radius:10px;max-width:100%" loading="lazy"></iframe>
Paste this URL in WordPress, Medium, or any oEmbed-compatible platform.
https://chemfyi.com/entity//
Add a dynamic SVG badge to your README or docs.
[](https://chemfyi.com/entity//)
Use the native HTML custom element.
CH3COOH + C2H5OH ⇌ CH3COOC2H5 + H2O
Ikhtisar
Acetic acid reacts with ethanol in the presence of an acid catalyst to form ethyl acetate and water. This reversible condensation reaction is the classic Fischer esterification. The equilibrium is driven to the right by using excess alcohol or removing water. Ethyl acetate has a characteristic fruity smell.
Peserta
| Peran | Zat | Koefisien | Keadaan |
|---|---|---|---|
| Reaktan | Acetic Acid CH₃COOH | 1 | (l) |
| Reaktan | Ethanol C₂H₅OH | 1 | (l) |
| Produk | Water H₂O | 1 | (l) |
Contoh Sehari-hari
The fruity smell of nail polish remover is ethyl acetate produced by this esterification reaction. Many fruit flavors are esters made similarly.
Pentingnya dalam Industri
Ethyl acetate is the world's most widely used organic solvent, produced at over 3 million tonnes annually for coatings, adhesives, and pharmaceutical extractions.
Sifat
- Jenis
- Organic
- Dapat Dibalik
- Ya
- Energi
- Eksoterm
- ΔH
- -10,0 kJ/mol
- Katalis
- Concentrated sulfuric acid