Reaction of camphor with an aromatic amine can be achieved using 10% zinc chloride as a catalyst in a suitable organic solvent under reflux conditions.
See "Preparation and reduction of camphor imines" - Bolton, Danks & Paul. Dept of Chem, University of Surrey, 1994.
The abstract of the paper does not identify which solvent is used, reflux time or product yield.
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.
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.
ethylene diamine metal complex react with aldehyde. will it form schiff base?
what is the compound of schiff base?1,8-diamino naphthalen and glyoxalic acid,1,5_diamino naphthalene and glyoxalic acid
If you are referring to a primary amine (RNH2), the shape of the amine part is pyramidal, unless the R group is aromatic (such as phenylamine), in which case the amine part is planar. If you are referring to the Schiff base (RNH2+), the amine component is also planar. If you are referring to the amide ion (NH2-), this has two lone pairs and is a bent molecule just like water.
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.
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.
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?
what is the compound of schiff base?1,8-diamino naphthalen and glyoxalic acid,1,5_diamino naphthalene and glyoxalic acid
How am I suppose to know huh
If you are referring to a primary amine (RNH2), the shape of the amine part is pyramidal, unless the R group is aromatic (such as phenylamine), in which case the amine part is planar. If you are referring to the Schiff base (RNH2+), the amine component is also planar. If you are referring to the amide ion (NH2-), this has two lone pairs and is a bent molecule just like water.
piperidine
Hugo german scientist
Ethylamine is a primary amine and is an alkaline compound.
Because methyl is an electron pumping group and It pumps electrons to Amine group to make it basic, But Ammonia has no influence from any basic groups. Therefore compared to Methyl-Amine, Ammonia is less basic