Why Dry Ether Is Used In Woods Reaction

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Why Dry Ether Is Used In Woods Reaction. The mechanism involved is free radical as well as anionic mechanism. Dry ether is a solvent which does not react with sodium.

General Chemistry III (Chem EH 301) Solved Question 2019 Section II from www.fdiengdoh.com

In wurtz reaction, dry ether, or acetone usually, acts as a solvent. The mechanism involved is free radical as well as anionic mechanism. The mechanism involved is free radical as well as anionic mechanism.

The Mechanism Involved Is Free Radical As Well As Anionic Mechanism.

If any polar solvent like water is used, it will ionize sodium and may result in some oxides or hydroxides of na or. In either of the mechanism na will loose an electron and form sodium ion. Also the alkyl halide used in the reaction should be.

In Wurtz Reaction, Dry Ether, Or Acetone Usually, Acts As A Solvent.

Dry ether is a solvent which does not react with sodium. Alkyl halides when reacted with na in presence of dry ether give alkanes. This is taken because, we want the sodium to react with the halogen in the organic compound.

Wurtz Reaction Is Carried Out With Sodium Metal Which Is Highly Reactive, Hence, We Have To Select A Solvent Which Will Not React With The Sodium Metal.

As a lewis base for na. In wurtz reaction sodium metal is used which is very reactive. So that the moisture can be absorbed by dry ether, because the sodium will react with moisture to form naoh and other complexes.

So Selection Of The Solvent Is Done In Such A Way That The Sodium Metal Does Not React With The Solvent.

The mechanism involved is free radical as well as anionic mechanism.