Is sodium phenoxide soluble in water?
Specifications
| Sensitivity | Air Sensitive |
|---|---|
| Solubility Information | Very soluble in water,soluble in alcoholSoluble in water,acetone and alcohol. |
| Formula Weight | 116.09 |
| Percent Purity | 98% |
| Chemical Name or Material | Sodium phenoxide |
What is sodium phenolate soluble in?
water
Soluble in water. In both cases, a corrosive alkaline solution forms that is a strong irritant to skin and eyes. Salts, basic, such as SODIUM PHENOLATE, are generally soluble in water.
Is C6H5ONa a salt?
Sodium phenolate (C6H5ONa) is a sodium salt of phenol, therefore we know that it is a weak base.
Why is phenoxide soluble in water?
Phenol is also soluble in water to some extent. It is due to its ability to form hydrogen bonding with water molecules. However the large part of phenol molecule is phenyl group that is non polar and hence its solubility if limited in water. However the polarity of this part too increases in phenoxide ion.
Is C6H5ONa ionic or covalent?
Explanation: As C6H5ONa can be dissociated as C6H5O- and Na+… there exists ionic bond.
What is the name of C6H5ONa?
Sodium phenoxide
| PubChem CID | 4445035 |
|---|---|
| Structure | Find Similar Structures |
| Chemical Safety | Laboratory Chemical Safety Summary (LCSS) Datasheet |
| Molecular Formula | C6H5NaO |
| Synonyms | Sodium phenoxide SODIUM PHENOLATE 139-02-6 Phenolate sodium Sodium phenate More… |
What happens when sodium phenolate reacts with iodomethane?
Sodium phenoxide reacts with methyl iodide and gives anisole.
Why is alcohol soluble in water?
Because alcohols form hydrogen bonds with water, they tend to be relatively soluble in water. The hydroxyl group is referred to as a hydrophilic (“water-loving”) group, because it forms hydrogen bonds with water and enhances the solubility of an alcohol in water.
Why does ethanol dissolve in water?
Ethanol is an alcohol that is soluble in water. This is because of the hydroxyl group (−OH) in the ethanol that is able to form hydrogen bonds with the water (H2O) molecules. The intermolecular hydrogen bonding is very high in the ethanol that is why it is soluble.
Is C6H5ONa ionic?
Is Phenolate a strong base?
However, phenol is sufficiently acidic for it to have recognizably acidic properties – even if it is still a very weak acid. A hydrogen ion can break away from the -OH group and transfer to a base. For example, in solution in water: Phenol is a very weak acid and the position of equilibrium lies well to the left.
When sodium phenoxide is treated with chloromethane the product obtained is?
Explanation: Chemical formula of sodium phenoxide is which is an alkoxide and chemical formula of methyl chloride is which is a halide. So, when an organohalide chemically reacts with a deprotonated alcohol then it results in the formation of an ether and this process is known as Williamson ether synthesis.