dicinnamalacetone and water
No, because when you add acetone to acetone, all you are doing is adding more of the volume of acetone to acetone. You are just changing the amount of acetone, not anything chemically happening.
When acetone bisulfite reacts with HCl, sulfur dioxide gas is evolved.
When acetone reacts with mercuric chloride and sodium hydroxide, the mercuric chloride will likely form a complex with acetone, while sodium hydroxide will react to form the sodium salt of acetone. This reaction can be used in the iodofom test to detect the presence of methyl ketones.
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
Chloroform can be converted into acetone through a series of reactions. Initially, chloroform undergoes oxidative cleavage to form phosgene, which then reacts with water to yield formic acid and hydrochloric acid. Further oxidation of formic acid produces carbon dioxide and water, while hydrochloric acid is neutralized with a base to form water and salt. Finally, the remaining product after this series of reactions is acetone.
No, because when you add acetone to acetone, all you are doing is adding more of the volume of acetone to acetone. You are just changing the amount of acetone, not anything chemically happening.
When acetone bisulfite reacts with HCl, sulfur dioxide gas is evolved.
Assuming there is water present, I would expect the product to be a (roughly equal) mixture of 2-octanol and 3-octanol.
One hydrazine reacts with two acetone to yield two 2-propanol and one nitrogen (gas).
When acetone reacts with mercuric chloride and sodium hydroxide, the mercuric chloride will likely form a complex with acetone, while sodium hydroxide will react to form the sodium salt of acetone. This reaction can be used in the iodofom test to detect the presence of methyl ketones.
An iodoform reaction is the type of reaction when acetone reacts with triiodomethane.
Chloroform can be converted into acetone through a series of reactions. Initially, chloroform undergoes oxidative cleavage to form phosgene, which then reacts with water to yield formic acid and hydrochloric acid. Further oxidation of formic acid produces carbon dioxide and water, while hydrochloric acid is neutralized with a base to form water and salt. Finally, the remaining product after this series of reactions is acetone.
Acetone can react with Grignard reagents to form alcohols, which can hinder the desired reaction. Additionally, acetone can also quench Grignard reagents by reacting with them before they can react with the desired substrate. Therefore, acetone is not an ideal solvent for reactions involving Grignard reagents.
martinium reacts fast while wellemium still reacts but much slower
ZnCl2 and Cu
Nitric acid.
The product of the reaction.