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∙ 15y agoAcetminophen is solube in 5% NaOH, and phenacetin is not because acetminophen is a stronger acid than water, and phenacetin is not appreciably acidic.
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∙ 15y agoPhenacetin will have a higher Rf value than acetaminophen in a TLC separation on silica gel using a non-polar developing solvent. This is because phenacetin is more non-polar than acetaminophen, causing it to move further up the TLC plate and have a higher Rf value.
Salicylic acid is slightly soluble in 10 percent sodium hydroxide due to ionization of the carboxylic acid group, forming the salicylate ion. However, it is not highly soluble compared to other compounds due to its limited solubility.
Phenacetin is soluble in water and organic solvents like ethanol and acetone. Its solubility in water is limited, typically around 1-2 g/L at room temperature.
Aluminium hydroxide is not soluble in water.
Yes, sucrose is soluble in sodium hydroxide. When mixed with sodium hydroxide in water, sucrose will dissolve to form a clear solution.
Among common metal hydroxides, potassium hydroxide (KOH) is the most soluble in water.
No, sodium hydroxide is not soluble in oil due to its hydrophilic nature. Sodium hydroxide is a strong base that is soluble in water but will not dissolve in nonpolar solvents like oil.
Most hydroxide compounds are soluble in water. However, the solubility can vary depending on the specific hydroxide compound. Common hydroxide compounds like sodium hydroxide (NaOH) and potassium hydroxide (KOH) are highly soluble in water.
No, not all metal hydroxides are soluble in water. Alkaline earth metal hydroxides like calcium hydroxide and barium hydroxide are sparingly soluble, while alkali metal hydroxides like sodium hydroxide and potassium hydroxide are highly soluble.
Ethanoic acid is fully soluble in water, but it will react with sodium hydroxide.
Yes, phenol is soluble in sodium hydroxide due to the formation of the water-soluble sodium phenolate salt. Phenol reacts with sodium hydroxide to form sodium phenolate and water.
Yes, cyclohexanol is soluble in aqueous sodium hydroxide because it can undergo deprotonation to form the water-soluble cyclohexoxide ion.