How is propan-1-ol synthesised by using Grignard reagent ?
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CH3-CH3-CH2OH + R-MgX ---> CH3CH3CH2-OMgX + R-H(alkane)
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Propan-1-ol synthesised by using Grignard reagent and reacting it with formaldehyde.
Explanation:
- The addition of magnesium metal to alkyl or alkenyl halides produces Grignard reagents. Cl, Br, or I can be used as the halide (not F). However, making Grignards from iodides and bromides is slightly easier.
- The Grignard reagent is reacted with formaldehyde to make a primary alcohol. A secondary alcohol is formed when a Grignard reagent is combined with any other aldehyde. Finally, a tertiary alcohol is produced by reacting a Grignard reagent with a ketone.
- Formaldehyde reacts with Grignard reagent to generate a complex, C2H5 – Mg – I in dry ether, which is then hydrolyzed with dilute HCI to form Propan-l-ol.
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