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.
Naphthalene is said to be somewhat soluble in ethyl alcohol (ethanol). It is insoluble in water and very soluble in ether, chloroform, or carbon disulfide.
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.
HCl is not soluble in ethyl acetate. It typically forms a separate layer in the presence of ethyl acetate due to their immiscibility.
Yes, benzoic acid is soluble in ethyl acetate. Both substances are organic compounds and generally have good solubility in each other.
Solubility of ethyl acetate (ethyl ethanoate) in water is 8.3 g/100 mL at 20 °C.
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.
Ethylacetate is soluble only in organic solvents.
Bromine is not soluble in either ethyl acetate or methanol. It would exist as separate liquid phases in the mixture due to differences in polarity and solubility. Bromine is slightly soluble in water, but not in most organic solvents like ethyl acetate or methanol.
Commonly sodium chloride is not dissolved in organic compounds.
The IUPAC name of ethyl acetate is ethyl ethanoate.
Ethyl iodide will undergo an SN2 reaction with potassium acetate to form ethyl acetate and potassium iodide. This reaction involves the substitution of the iodine atom in ethyl iodide with the acetate ion from potassium acetate.
Practically insoluble in water, in glycerol, and in propane-1,2-diol, but soluble in varying proportions in certain organic solvents, depending upon the ethoxyl content. Ethyl cellulose containing less than 46-48% of ethoxyl groups is freely soluble in tetrahydrofuran, in methyl acetate, in chloroform, and in aromatic hydrocarbon ethanol mixtures. Ethylcellulose containing 46- 48% or more of ethoxyl groups is freely soluble in ethanol, in methanol, in toluene, in chloroform, and in ethyl acetate.