diazotized
sulfanilic
acid
The chemical formula for sulfanilic acid is C6H7NO3S.
C6H7NO3S
When you attempt to prepare sulfanilamide from this reagent, a polymeric product is produced after the addition of PCL5 in step one. So no, this is not typically a reaction used to prepare sulfanilamide.
Vanillin, an aldehyde compound, can react with a variety of reagents in different types of reactions. For example, vanillin can undergo condensation reactions with amines to form imines, or react with nucleophiles like Grignard reagents to form alcohol derivatives. Vanillin can also be oxidized to vanillic acid using oxidizing agents like chromic acid.
4-[(2-hydroxy-1-naphthalenyl)azo]phenyl chloride monosodium salt
When sulfanilic acid, 1-naphthylamine, and sodium nitrite are mixed together in solution, a reddish-pink color is typically observed. This color change is due to the formation of a diazo dye known as azo dye, which is commonly used in dyeing processes.
No, conglomerate does not react to acid.
The reagent used in Pauly's reaction is α-naphthol and concentrated hydrochloric acid. This reagent system is used to test for the presence of indole-like compounds in organic molecules.
Ortho sulfanilic acid is more stable than meta sulfanilic acid because the ortho position allows for greater resonance stabilization of the negative charge on the deprotonated form. In the ortho position, the negative charge can be delocalized over two oxygen atoms, leading to enhanced stability. Conversely, in the meta position, there is no such resonance stabilization, resulting in lower stability.
Plutonium easily react with nitric acid.
Germanium does not react with hydrochloric acid at room temperature. However, it can react with hydrochloric acid when heated, forming germanium chloride.
Gold react with aqua regia not with hydrochloric acid.