pH is amplified in logs of 10. For example, a reading of 6 pH is 10 times more acidic than that of 7 and 6 pH is 100 times more acidic than 8 pH. Since 7-3=4, a pH of 3 is 104 or 10,000 times more acidic than a pH of 7.
Yes, NO2 is more acidic than CO2.
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.
a lemon is more sour than a grapefruit because it is more acidic.
Alkynes are more acidic than alkenes and alkanes. Alkenes are more acidic than alkanes.
No, water is neutral with a pH of 7. Phenol is slightly acidic with a pH range between 5 and 6.
10^4 as each pH is equal to 10 times difference so an acid of pH 7 would be 104 weaker than an acid of pH 3
Yes, NO2 is more acidic than CO2.
Anything with a pH of more than 7 is not acidic at all, it is alkaline.
100
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.
To determine how much more acidic one number is than another on a pH scale, we use the fact that each whole number change in pH represents a tenfold change in acidity. Therefore, a pH of 2 is 10^3 (or 1,000 times) more acidic than a pH of 5, since the difference between 2 and 5 is three units.
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 embalming fluids used in the arteries and body cavity are essentially the same. The difference is the body fluid is slightly more acidic than the arterial fluid. It is also sometimes scented.
18 quarts is much more
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.