Yes,it is more acidic.It is way stronger.
HNO3 is stronger than HNO2 because it has one more oxygen atom, making it a stronger acid. The presence of more oxygen atoms leads to greater electronegativity and more stability in the resulting conjugate base after donating a proton, resulting in increased acidity.
Sulfuric acid is generally considered more acidic than nitric acid. This is due to sulfuric acid's ability to donate two protons in solution, making it a stronger acid. Nitric acid can only donate one proton.
Nitric acid (HNO3) is stronger than nitrous acid (HNO2) as its conjugate base is more stable, leading to a more acidic solution. Nitric acid is a strong acid that completely dissociates in water, while nitrous acid is a weaker acid that only partially dissociates.
Yes, NO2 is more acidic than CO2.
An ACIDIC Sol'n has a pH < 7. pH = 1 is strongly acidic (H2SO4/HCl/HNO3) pH = 4 mildly acidic (CH3COOH) pH = 6 weakly acidic. (H2CO3 as naturak rain water; NOT acidic rain).
Anything with a pH of more than 7 is not acidic at all, it is alkaline.
No, beer is actually less acidic than wine.
Resorcinol is more acidic than catechol. This is because resorcinol has three -OH groups that are more acidic than the two -OH groups in catechol.
No, pH 9 is actually more basic (alkaline) than pH 4. The pH scale is logarithmic, so each unit is 10 times more acidic or basic than the unit next to it. pH 4 is more acidic than pH 9.
The presence of sulfur dioxide (SO2) and nitrogen oxides (NOx) in the atmosphere can react with water vapor and form sulfuric acid (H2SO4) and nitric acid (HNO3), making the rain more acidic than natural rainwater. These pollutants are primarily released by human activities such as burning fossil fuels and industrial processes.
No, a pH of 5 is ten times more acidic than a pH o6.
Imides are more acidic than amides because the hydrogen atom in imides is present on a nitrogen atom that is more electronegative than the oxygen atom in amides. This greater electronegativity leads to a more stable conjugate base after deprotonation, making the imide more acidic.