Commonly sodium chloride is not dissolved in organic compounds.
No, sodium chloride is not soluble in ethyl acetate. Ethyl acetate is a nonpolar solvent, while sodium chloride is an ionic compound that is highly soluble in water but not in nonpolar solvents like ethyl acetate.
Sodium chloride is insoluble in ethyl alcohol because the bonding between sodium and chloride ions in sodium chloride is very strong due to ionic attractions. Ethyl alcohol is a non-polar solvent, which cannot break these strong ionic bonds to dissolve sodium chloride.
No, sugar does not dissolve in ethyl acetate because sugar is a polar molecule that is more likely to dissolve in polar solvents like water. Ethyl acetate is a nonpolar solvent and is not capable of dissolving polar substances like sugar.
The reaction between sodium hydride and ethyl acetate would likely result in the formation of sodium acetate and hydrogen gas. Sodium hydride would react with the acidic hydrogen in ethyl acetate to form sodium acetate, while releasing hydrogen gas as a byproduct.
To prepare 200ml of 0.1 N ethyl acetate solution, you will need to calculate the amount of ethyl acetate needed. Since the molecular weight of ethyl acetate is around 88.11 g/mol, for 200ml of 0.1 N solution, you would need around 1.76g of ethyl acetate. Dissolve this amount of ethyl acetate in distilled water to make up the final volume to 200ml.
Sodium Chloride has a higher melting point because at room temperature it is a solid but Ethyl alcohol has already melted, as it is liquid.
The sodium carbonate solution is used in the experiment to neutralize any acidic impurities present in the ethyl acetate. This helps to ensure that the ethyl acetate is pure and free from any acidic contaminants that could interfere with the desired reaction or analysis.
Naphthalene is soluble in ethyl acetate due to their similar polarities and the nature of their interactions. Naphthalene is a nonpolar aromatic hydrocarbon, while ethyl acetate is a polar aprotic solvent; however, ethyl acetate has a significant nonpolar character due to its hydrocarbon tail. The dispersion forces and dipole-induced dipole interactions between the nonpolar parts of naphthalene and ethyl acetate facilitate its solubility. As a result, naphthalene can dissolve in ethyl acetate, making it an effective solvent for extracting or dissolving naphthalene.
benzene, toluene, chloroform, dichloromethane, ethyl acetate
If a sample of water is soluble in ethyl acetate, you would observe the formation of a clear solution after mixing the two liquids. Ethyl acetate is a nonpolar solvent, so it is expected to dissolve nonpolar substances like oils, fats, and some organic compounds that may be present in the water sample.
Yes, ethanol belongs to the alcohol functional group therefore polar, and BaCl2 is polar, so it does dissolve.
The IUPAC name of ethyl acetate is ethyl ethanoate.