Grignard Reaction with Formaldehyde
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.
CH3MgBr + HCHO → CH3CH2OH (after hydrolysis)
Visão geral
A Grignard reagent (methylmagnesium bromide) adds to formaldehyde, and after aqueous workup produces a primary alcohol. Grignard reagents are organomagnesium halides that act as powerful nucleophilic carbon sources. The reaction must be performed in anhydrous ether because Grignard reagents react violently with water.
Participantes
| Papel | Substância | Coeficiente | Estado |
|---|---|---|---|
| Reagente | Formaldehyde CH₂O | 1 | (l) |
| Produto | Ethanol C₂H₅OH | 1 | (l) |
Exemplo do cotidiano
Victor Grignard won the 1912 Nobel Prize for this reaction, which revolutionized organic synthesis and is still one of the most taught reactions.
Importância industrial
As reações de Grignard são utilizadas na síntese de álcoois, ácidos carboxílicos e compostos orgânicos complexos. São fundamentais na indústria farmacêutica e agroquímica. Victor Grignard recebeu o Prémio Nobel da Química em 1912.
Propriedades
- Tipo
- Organic
- Reversível
- Não
- Energia
- Exotérmico
- ΔH
- -85,0 kJ/mol