Diazonium salts are unstable compounds, aromatic diazonium compound on hydrolysis give phenol and Nitrogen gas.
C6H5-N2+Cl- + NaOH(Aq.) = C6H5-OH + N2 + NaCl
The reason is that the aryl group is able to stabalize the diazonium salt through resonance, while the alkyl group may not be resonance stabalized.
Because diazonium ions are unstable at room temperature and become decomposed giving the Nitrogen gas.
Because diazonium ions are unstable at room temperature and they can decompose
yes it is a neutral salt
activated rings of phenol and aromatic amines-- that is based from the manual. you can read it if you like...
The reason is that the aryl group is able to stabalize the diazonium salt through resonance, while the alkyl group may not be resonance stabalized.
Because diazonium ions are unstable at room temperature and become decomposed giving the Nitrogen gas.
Check the spelling: probable you think to disodium or diazonium.
Diazonium means, Di=2, azo=nitrogen and ium= +charge, so two nitrogen atoms having positive charge is a diazonium ion, when such ion is attached to alkyl group it is Alkyl diazonium ion and a negative ion attached to this ion means alkyl diazonium salt as R-N2+Cl-
Because diazonium ions are unstable at room temperature and they can decompose
the reaction in which cation or anions of salts reacts with water to produce acid or base is called salt hydrolysis.
hydrolysis gives glucose and fructose
Not sure either, but i would guess that it is to protonate the oxygens so that they can leave?
yes it is a neutral salt
In the presence of sodium nitrite and hydrochloric acid, sulfanilc acid form a diazonium salt. This salt react with and is an indicator for thyrosine, histidine.
activated rings of phenol and aromatic amines-- that is based from the manual. you can read it if you like...
This is a "reaction" with water, a dissociation of the salt in ions.