No, although an imine is prepared in situ in a mannich reaction. A schiff base can be prepared when a starting primary amine reacts with a ketone or aldehyde and liberates a water molecule.
Why formaldehyde use in mannich base reaction
what is the compound of schiff base?1,8-diamino naphthalen and glyoxalic acid,1,5_diamino naphthalene and glyoxalic acid
yes it can be prepared as glucose has an aldehyde group and for preparartion of Schiff base we need a aldehyde or ketone and a primary amine.... glucose can be used as aldehyde.
`because of aromatic ring nitrogen lone pair will participate in resonance which make the acidic amine,that's why
ethylene diamine metal complex react with aldehyde. will it form schiff base?
Why formaldehyde use in mannich base reaction
it is possible to product mannich base using acetophenone with DEA.
what is the compound of schiff base?1,8-diamino naphthalen and glyoxalic acid,1,5_diamino naphthalene and glyoxalic acid
yes it can be prepared as glucose has an aldehyde group and for preparartion of Schiff base we need a aldehyde or ketone and a primary amine.... glucose can be used as aldehyde.
`because of aromatic ring nitrogen lone pair will participate in resonance which make the acidic amine,that's why
hi, schiff base is so called because Hugo schiff was discover it
Schiff base was proposed by Hugo Schiff and are imines that are formed by the condensation of aldehydes or ketones with primary amines.
ethylene diamine metal complex react with aldehyde. will it form schiff base?
Hugo german scientist
Salts are prepared by a reaction between an acid and a base; the insoluble salt is a precipitate.
aniline and benzaldehyde combines to form a C6H5N=CHH5C6 type of imine
Schiff bases are imines formed by the condensation of aldehydes or ketones with primary amines. The mobile phase for this could be ethyl acetate in hexane or chloroform in methanol.