What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?y
Policyclic non-aromatic (alicyclic) compounds, I believe.
ever heard of a molitov?
Aromatic rings tend to be more stable than non-aromatic rings, if that's what you're asking. I'm not quite sure what the question means.
The short answer is "yes." However, in chemistry, "aromatic" has a specific meaning that might be different from what a non-chemist would probably guess, and many scents are not aromatic in the chemical sense. Incidentally, many natural scents contain the exact same aromatic hydrocarbons used in some artificial scents.
What is the chemical reaction for furfural and a primary aromatic amine C5H4O2 plus Nh2?y
Their orbitals unsymmetry make them unstable.
Biphenyl is a non planar molecule and hence should'nt be aromatic.
yes
Policyclic non-aromatic (alicyclic) compounds, I believe.
Furfural is furan-2-carboxaldehyde, a heterocyclic aldehyde. A colorless, sweet-smelling, mobile liquid, C4H3OCHO, made from corncobs and used in the synthesis of furan, as a solvent for nitrocellulose, and as a fungicide and weed killer.
ever heard of a molitov?
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No. It is an aldehyde. Furfural is furan-2-carboxaldehyde.
Aromatic rings tend to be more stable than non-aromatic rings, if that's what you're asking. I'm not quite sure what the question means.
The short answer is "yes." However, in chemistry, "aromatic" has a specific meaning that might be different from what a non-chemist would probably guess, and many scents are not aromatic in the chemical sense. Incidentally, many natural scents contain the exact same aromatic hydrocarbons used in some artificial scents.
This process is the identification of carbohydrates. One may draw the structure of the adduct two molecules of resorcinol with 1 molecule of furfural to obtain carbohydrates.