Cyclohexanone and benzophenone are both non-polar. Water is polar. "Like dissolves like" so non-polar substances dissovle other non-polar substances and polar substances dissolve other polar substances.
Cyclohexanone is slightly soluble in water, with a solubility of around 6.6 g/L at room temperature. This solubility is due to the polar carbonyl group present in cyclohexanone that can interact with water molecules through hydrogen bonding.
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.
Benzophenone is partially soluble in hexane. Benzophenone is polar, where as, hexane is nonpolar. "Like dissolves like."
Yes it is definitely soluble in methyl alcohol through experimental observation but to the extent of polarity is what i am trying to figure out. There should be a difference in solubility of benzophenone in methyl alcohol and in hexane. It is def. partially soluble in hexane and im guessing it is suppose to be completely soluble in methyl alcohol. I must have just messed up in the lab
From least to most polar: biphenyl >> benzophenone >> benzhydrol
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.
Cyclohexanone is slightly soluble in water, with a solubility of around 6.6 g/L at room temperature. This solubility is due to the polar carbonyl group present in cyclohexanone that can interact with water molecules through hydrogen bonding.
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.
Benzophenone is partially soluble in hexane. Benzophenone is polar, where as, hexane is nonpolar. "Like dissolves like."
Benzophenone dissolves non-polar molecules better than water. It is commonly used in preparing pure and anhydrous solvents because it removes moisture and oxygen unlike water.
The chemical formula for cyclohexanone is C6H10O
Cyclohexanone can be oxidized to adipic acid.
Yes it is definitely soluble in methyl alcohol through experimental observation but to the extent of polarity is what i am trying to figure out. There should be a difference in solubility of benzophenone in methyl alcohol and in hexane. It is def. partially soluble in hexane and im guessing it is suppose to be completely soluble in methyl alcohol. I must have just messed up in the lab
From least to most polar: biphenyl >> benzophenone >> benzhydrol
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.
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.
Yes, Tollens' reagent can react with cyclohexanone. Tollens' reagent is commonly used to test for the presence of aldehydes, including cyclohexanone, by forming a silver mirror when the aldehyde is present.