Not to any appreciable extent.
Yes, ethanol belongs to the alcohol functional group therefore polar, and BaCl2 is polar, so it does dissolve.
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.
water is more dense than ethyl acetate , so water remains on bottom and ethyl acetate on top when both mixed.
Sodium Acetate Can be fond in 2 forms. Either anhydrous or trihydrate. Oxidation reaction with anhydrous form is easier than trihydrate form. First form has reaction similar to that of Oxidation of Acetic Acid. Trihydrate form is a bit more complex and I'm still loking into it
Commonly sodium chloride is not dissolved in organic compounds.
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.
Yes, ethanol belongs to the alcohol functional group therefore polar, and BaCl2 is polar, so it does dissolve.
Solubility of ethyl acetate (ethyl ethanoate) in water is 8.3 g/100 mL at 20 °C.
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.
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.
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.
Ethylacetate is soluble only in organic solvents.
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.
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.