The diazonium molecule includes a nitrogen atom with a quadruple bond. Nitrogen has 3 valance electrons and normally forms a triple bond. The quadruple bond is highly unstable for nitrogen, and therefore, it can easily fail, leading to immediate and dramatic chemical change, which we observe in the form of an explosion.
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.
Diazonium salts are unstable compounds, aromatic diazonium compound on hydrolysis give phenol and Nitrogen gas. C6H5-N2+Cl- + NaOH(Aq.) = C6H5-OH + N2 + NaCl
Because diazonium ions are unstable at room temperature and they can decompose
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 salts are unstable compounds, aromatic diazonium compound on hydrolysis give phenol and Nitrogen gas. C6H5-N2+Cl- + NaOH(Aq.) = C6H5-OH + N2 + NaCl
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
Not sure either, but i would guess that it is to protonate the oxygens so that they can leave?
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...
the intermediate positively charged nitrogen is being supplied by large electron clouds coming from both sides, i.e., the intermediary triple bonds with the other N that is attached to a conjugate base (that's why it is a diazonium salt) and the pi electron cloud from the benzene ring.... this makes the aromatic diazonium salt much more stable on the other hand, the intermediate positively charged nitrogen is much less stable due to a weak van der waals and london forces coming from the aliphatic alkyl chain although the intermediary triple bonds of another nitrogen is near-by. thus, it is the large pi electron cloud of the aromatic ring which stabilies the positively charged nitrogen of the diazonium salt
The hydrogen bomb is the most powerful bomb ever tested.
the chemicals used in a grenead are many explosve elements like ZnO and PbO