0
The melting point for lauric acid is about 45 degrees while it is 121 degrees for naphthol. So, in a mixture repeated cycles of slow warming and cooling should separate out lauric acid from naphthol. You can improve the efficiency by adding a dash of slightly acidic 70% isopropyl alcohol. This will deprotonate the lauric acid while maintaining the proton on naphthol during this process to enhance separation and purification of the two compounds. You could also flat-out distill the two products by maintaining the temperature of the solution at the boiling point of lauric acid to separate it from naphthol.
What else can I help you with?
Is benzophenone soluble in hexane?
Benzophenone is partially soluble in hexane. Benzophenone is polar, where as, hexane is nonpolar. "Like dissolves like."
What is the increasing polarity order of bi phenyl benzhydrol benzophenone?
From least to most polar: biphenyl >> benzophenone >> benzhydrol
How would you convert benzophenone into benzanilide?
Benzophenone can be converted into benzanilide by reacting it with aniline in the presence of a base, such as potassium hydroxide. The reaction proceeds via nucleophilic aromatic substitution, where the aniline replaces the oxygen in benzophenone, forming benzanilide. The product can be isolated and purified by techniques such as recrystallization.
Are hexane and benzophenone soluble or insoluble?
Hexane is insoluble in water, while benzophenone is slightly soluble in water. Both hexane and benzophenone are soluble in organic solvents such as ether, acetone, and chloroform.
Are diphenylmethanol and benzophenone created in a one to one ratio?
The question here is asked in a slightly incorrect manner. Assuming I understand exactly what you meant to ask which is "In a reduction of Benzophenone is Diphenylmethanol created with a 1/1 molar ratio?" then the answer is yes they are. For every mole of benzophenone one mole of diphenylmethanol is created. Benzophenone is a reagent and diphenylmethanol is a product in a reduction of benzophenone reaction. However if you're referring to a reaction which creates BOTH diphenylmethanol and benzophenone as products, then you would need to provide the reagents that create the two.
Is benzophenone soluble in hexane?
Benzophenone is partially soluble in hexane. Benzophenone is polar, where as, hexane is nonpolar. "Like dissolves like."
What is the increasing polarity order of bi phenyl benzhydrol benzophenone?
From least to most polar: biphenyl >> benzophenone >> benzhydrol
How would you convert benzophenone into benzanilide?
Benzophenone can be converted into benzanilide by reacting it with aniline in the presence of a base, such as potassium hydroxide. The reaction proceeds via nucleophilic aromatic substitution, where the aniline replaces the oxygen in benzophenone, forming benzanilide. The product can be isolated and purified by techniques such as recrystallization.
Are hexane and benzophenone soluble or insoluble?
Hexane is insoluble in water, while benzophenone is slightly soluble in water. Both hexane and benzophenone are soluble in organic solvents such as ether, acetone, and chloroform.
Are diphenylmethanol and benzophenone created in a one to one ratio?
The question here is asked in a slightly incorrect manner. Assuming I understand exactly what you meant to ask which is "In a reduction of Benzophenone is Diphenylmethanol created with a 1/1 molar ratio?" then the answer is yes they are. For every mole of benzophenone one mole of diphenylmethanol is created. Benzophenone is a reagent and diphenylmethanol is a product in a reduction of benzophenone reaction. However if you're referring to a reaction which creates BOTH diphenylmethanol and benzophenone as products, then you would need to provide the reagents that create the two.
What solvent would you use to measure the density of benzophenone?
You can measure the density of benzophenone using solvents like toluene, ethanol, or chloroform. These solvents can dissolve benzophenone and provide an accurate density measurement.
Is benzophenone soluble in 95 percent ethyl alcohol?
Yes, benzophenone is soluble in 95% ethyl alcohol. Benzophenone is a nonpolar compound and ethanol is a polar solvent, but benzophenone is still soluble in ethanol due to its relatively small molecular size and the presence of some nonpolar regions.
Why is Benzophenone commonly used with clear or glass packaging?
Benzophenone prevents ultraviolet light from damaging colors and scents in products. Without the use of benzophenone some products would have to be shipped in black or dark packaging for protection.
What functional groups are present in the infrared spectrum of benzophenone?
The functional groups present in the infrared spectrum of benzophenone are carbonyl (CO) and aromatic (CC) groups.
How many moles required to reduce benzophenone to diphenylmethanol using sodium borohydride?
One mole of benzophenone requires one mole of sodium borohydride for reduction to diphenylmethanol.
The cotton gin was a machine that could?
seperate cotton from the cotton seeds and improved slavery
Attraction between benzophenone and methanol?
Benzophenone and methanol can exhibit some weak attraction forces, like dipole-dipole interactions due to the polar nature of methanol. However, the strength of these interactions is not as significant as in hydrogen bonding or other stronger types of intermolecular forces.
