Oxidation of Primary Alcohol to Aldehyde
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.
RCH2OH + [O] → RCHO + H2O
Обзор
Primary alcohols are oxidized to aldehydes using mild oxidizing agents like PCC or Dess-Martin periodinane. Stronger oxidants (KMnO₄, CrO₃) would over-oxidize to the carboxylic acid. The carbon oxidation state changes from -1 to +1. Distilling the aldehyde product during reaction prevents over-oxidation.
Участники
| Роль | Вещество | Коэффициент | Состояние |
|---|---|---|---|
| Продукт | Water H₂O | 1 | (l) |
Пример из жизни
The formation of acetaldehyde from ethanol in the liver is this type of oxidation, responsible for hangover symptoms.
Промышленное значение
Selective alcohol oxidation to aldehydes is critical in perfume and flavor production and in pharmaceutical intermediate synthesis.
Свойства
- Тип
- Organic
- Обратимая
- Нет
- Энергия
- Экзотермическая
- ΔH
- -175,0 kJ/mol
- Катализатор
- PCC (pyridinium chlorochromate)