2
The nitrate ion, NO3^-, has 3 resonance structures.
To describe the structure of HNO3, two resonance structures are needed.
HNO3 is a chemical that has 1 hydrogen atom (HNO3), 1 nitrogen atom (H N O3) and 3 oxygen atoms (HN O3). If the queston meant what chemical HNO3 stood for, then the answer is nitric acid.WOuldn't it be call Nitrous acid? Since it is a Oxy acid..... ite----- turns to ous. just a suggestion.HNO3 is called Hydrogen Nitrate or Bi Nitrate.
3 oxygen atoms are found in one molecule of nitric acid.
There are three resonance structures of pyrimidines. These structures involve the delocalization of electrons within the aromatic ring of the molecule, leading to different arrangements of double bonds.
there are three resonating structures of H2CO3 OH+-------C------O+-------oh+
The number of nitric acid molecules is 28,6723.10e23.
The nitrate ion, NO3^-, has 3 resonance structures.
To describe the structure of HNO3, two resonance structures are needed.
HNO3 is a chemical that has 1 hydrogen atom (HNO3), 1 nitrogen atom (H N O3) and 3 oxygen atoms (HN O3). If the queston meant what chemical HNO3 stood for, then the answer is nitric acid.WOuldn't it be call Nitrous acid? Since it is a Oxy acid..... ite----- turns to ous. just a suggestion.HNO3 is called Hydrogen Nitrate or Bi Nitrate.
Nitric acid is dissociated in water in: (NO3)- and 2 H+.
There are three resonance structures possible for the permanganate ion (MnO4-).
There are two resonance structures for CHO2. The negative charge can be delocalized between the oxygen and the carbon atoms, giving two different structures.
No. However, many fertilizers do contain nitrates, such as ammonium nitrate which can be thought of as salts of nitric acid.
There are two resonance structures that can be drawn for O3 (ozone). This is because there is a double bond that can be delocalized between different oxygen atoms, resulting in two possible arrangements of bonds.
3 oxygen atoms are found in one molecule of nitric acid.
There are three resonance structures of pyrimidines. These structures involve the delocalization of electrons within the aromatic ring of the molecule, leading to different arrangements of double bonds.