The carbonyl group of the benzophenone acts as a hydrogen bond acceptor with the alcohol group of methanol.
It depends on what you added to the methanol before you put the heated copper wire into the methanol. The heated copper wire acted as a catalyst to speed up the reaction between the methanol and the other substance. Copper itself does not react with methanol.
Methanol is CH3OH, ethanol is CH3CH2OH. Both are alcohols, ethanol has one carbon more (or a CH2 group more) and is less polar than methanol. Also ethanol has higher boiling point than methanol.
distance between them. The greater the mass of the objects and the closer they are, the stronger the gravitational attraction between them.
The reaction between CH3CH2MgBr (ethylmagnesium bromide) and methanol results in the formation of ethanol and magnesium bromide. The balanced equation for this reaction is: CH3CH2MgBr + CH3OH -> CH3CH2OH + MgBr2
Methanol is an alcohol and consists of carbon,hydrogen and oxygen its formula is CH3OH
The intermolecular bond in methanol is hydrogen bonding due to the presence of hydrogen atoms bonded to oxygen. This results in methanol molecules being attracted to each other through strong dipole-dipole interactions.
The reduction of Benzophenone to Diphenylmethanone typically involves the use of a reducing agent such as sodium borohydride (NaBH4) in the presence of a proton source like methanol. NaBH4 donates hydride ions (H-) to the carbonyl group of Benzophenone, resulting in the formation of Diphenylmethanol which is then oxidized to Diphenylmethanone by reaction with an oxidant like chromic acid.
Benzophenone is partially soluble in hexane. Benzophenone is polar, where as, hexane is nonpolar. "Like dissolves like."
From least to most polar: biphenyl >> benzophenone >> benzhydrol
Methanol melts between -98oC and -97oC. It boils at 64.7oC.
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.
Methanol is CH3OH while ethanol is C2H5OH. The difference is CH2.
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.
Methanol is miscible with water, which means it can mix in any proportion. When methanol is added to water, it forms a homogenous solution due to hydrogen bonding interactions between the methanol and water molecules. This allows methanol to dissolve easily in water.
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.
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.
water have inter molecular hydrogen bonding whereas in methanol there is intra molecular hydrogen bonding.the oxygen atom and hydrogen of other molecule have electrostatic force of attraction in water and forms bridge between each other and form an associated structure thus it has more b.p