to convert the phthalic anhydride in to phthalimide, it is heated with urea at the temp. of 160 c with out using any solvent. phthalic anhydride + urea = phthalimide +water+ carbondioxide
acidic character
In gabriel synthesis on primary amines are formed. Secondary and tertiary amines are not formed this yields in pure rimary amine product. Hence Gabriel phthalimide synthesis is preferred for synthesising primary amines
no
because it is an organic compound and its functional group is co-oh which is an acid so due to its acidic functional group its characteristics became acidic
to convert the phthalic anhydride in to phthalimide, it is heated with urea at the temp. of 160 c with out using any solvent. phthalic anhydride + urea = phthalimide +water+ carbondioxide
acidic character
aromatic primary amine canot be synthesised by gabriel phthamide synthesys as aryl halide does not show nucliophilic substitution reaction
In gabriel synthesis on primary amines are formed. Secondary and tertiary amines are not formed this yields in pure rimary amine product. Hence Gabriel phthalimide synthesis is preferred for synthesising primary amines
It is a character who appears to show how the main character has changed.To show how a main character changes. appears to show how a primary character has changed.- APEX
no
because it is an organic compound and its functional group is co-oh which is an acid so due to its acidic functional group its characteristics became acidic
To show character you should describe the personality.
Yes it does. The lower the pH the more acidic the solution.
how acidic alkali or neutral a substance is.
Chlorine, nitrogen, and oxygen are highly electronegative and thus electron withdrawing, which makes it easy for a hydrogen atom to break off in HNO3 or HCl. Glucose, by contrast, contains carbon which is electron releasing, this makes it harder for a hydrogen ion to break off.
E. I'm not sure.