In this step of the experiment you are trying to separate benzoic acid from biphenyl an impurity. Sodium hydroxide reacts with benzoic acid to form (ar-O-O(-)na(+)) and (H2O), this allows for the ether layer containing biphenyl to separate as the precipitant, which we can now extract and discard.
It depends on the overall reaction. If the carboxylic acid is an impurity in the reaction (undesired), then washing with sodium hydroxide will extract the carboxylic into the aqueous layer, and it can then be disposed. The reaction for this looks as follows: (ring)-COOH + NaOH -> (ring)-COO-Na+ + H20 Where the ring loses a proton to the hydroxide ion and becomes water soluble.
No. Sodium chloride is polar, whereas diethyl ether is non-polar. Unlike solutes do not dissolve in unlike solvent. Only "like dissolves like".
The reaction between 1-propanol and ethyl bromide would result in an SN2 reaction where the ethyl bromide attacks the carbon bearing the -OH group on 1-propanol, displacing the hydroxyl group and forming ethyl propyl ether as the main product. Sodium hydroxide may be used as a catalyst in this reaction.
Naphthalene is nonpolar and therefore soluble in nonpolar solvents like ether, but not very soluble in the polar solvent water. Sodium chloride is ionic and soluble in water due to the strong ion-dipole interactions, but not soluble in ether which cannot stabilize the charged ions. The solubility of compounds in different solvents is primarily determined by the nature of the intermolecular interactions between the solute and solvent molecules.
No, ethyl acetate and diethyl ether are not the same. Ethyl acetate is an ester commonly used as a solvent, while diethyl ether is an ether used as a solvent and a reagent in chemical reactions. They have different chemical structures and properties.
It depends on the overall reaction. If the carboxylic acid is an impurity in the reaction (undesired), then washing with sodium hydroxide will extract the carboxylic into the aqueous layer, and it can then be disposed. The reaction for this looks as follows: (ring)-COOH + NaOH -> (ring)-COO-Na+ + H20 Where the ring loses a proton to the hydroxide ion and becomes water soluble.
No, sodium bicarbonate is not soluable in ether.
Classification of any substance as solute and solvent is not possible until it is being used along with other substance/s . The substance present in the largest quantity is solvent whereas substances present in smaller quantity which are able to get dissolved in the solvent are solute.
Nothing!
No. Sodium chloride is polar, whereas diethyl ether is non-polar. Unlike solutes do not dissolve in unlike solvent. Only "like dissolves like".
No.
Water, Sodium Laureth Sulfate, Dimethicone, Cocamidopropyl Betain, Cocamide MIPA, Distearyl Ether, Sodium Chloride, Behenyl Alcohol, Laureth-2, PPG-5-Ceteth-20, Pyrus Malus (Apple) Fruit Extract, Fragrance, Sodium Methylparaben, Carbomer, DMDM Hydantoin, Niacinamide, Pyridoxine HCl, Guar Hydroxypropyltrimonium Chloride, Citric Acid, Saccharum Officinarum (Sugar Cane) Extract, Citrus Medica Limonum (Lemon) Peel Extract, Camellia Sinensis Leaf Extract
Sodium metal being insoluble in ether is a physical property, not a chemical reaction. This is because no new substances are being formed, it is simply a case of the sodium metal not dissolving in the ether due to differences in polarity.
no, but it dissolves
Sodium chloride is not soluble in ether.
oxygen
Sodium chloride, sulfur, and methyl alcohol are insoluble in petroleum ether due to their polar nature and the non-polar characteristics of petroleum ether. Sodium chloride is an ionic compound, while sulfur is a nonpolar solid, and methyl alcohol, although polar, has a hydroxyl group that does not interact favorably with the predominantly nonpolar hydrocarbon chains of petroleum ether. This mismatch in polarity leads to poor solubility for these substances in petroleum ether.