Bronsted-Lowry acids are proton donors, and when mixed with water, hydrogen ions are released, forming hydronium ions, also known as hydronium ions, which are H3O+.
Bronsted-Lowry bases are proton acceptors, and when a base reacts with an acid, a hydronium ion is formed.
Diprotic acids like sulfuric acid produce two H+ ions for every acid molecule, so the concentration of the acid is two times the concentration of H+ ions.
The pH of a strong acid is calculated by assuming that strong acids dissociate fully and the concentration of H+ ions is equal to the concentration of the acid.
When calculating the pH of a strong base, it is assumed that the base dissociates fully to form OH- ions, and the concentration of the base equals the concentration of OH- ions.
To calculate the pH of a base, the concentration of H+ ions is needed, which can be found using the ionic product of water expression, KW.
For monoprotic acids like hydrochloric acid and nitric acid, the concentration of H+ ions is equal to the concentration of the acid.
Bronsted-Lowry acid-base equilibria is a concept in chemistry that explains how acids and bases work.
The buffer is made up of 0.1 moles of ethanoic acid, 0.1 moles of methanoic acid, and 0.1 moles of NaOH.
Calculations involve adding a small amount of an acid or base to a buffer and determining the change in pH.
When 10 centimeters cubed of one mole dilute hydrochloric acid is added to a decimetres cubed of buffer solution, the pH changes from 7 to 6.
The usual assumptions are used in calculations.
The change in pH is due to the buffer resisting the change.
When a base is added to a buffer, the hydroxide ions react with the H+ ions, shifting equilibrium to the right.
The minus log of H+ can be taken in the Ka expression.
A buffer is a system where two equilibrium equations exist in the same beaker.
An acidic buffer resists the change in pH in order to keep the solution below pH 7 and is made from a weak acid and its salt.
When an acid is added to a buffer, the H+ ions react with the athan iodine, shifting equilibrium to the left.
Salts associate and dissociate fully, meaning equilibrium is well to the right in a buffer.
An acidic buffer is made from a weak acid and its salt.
A buffer is made by using a weak acid and its salt, and must be the salt of the acid that is being used.
In a buffer solution, there are two equilibrium equations at play.
There are two types of buffer: acidic and basic.
The definition and determination of pH is a crucial aspect of AQA acids and bases.
The half neutralization point is the point halfway between zero and the equivalence point, which can be used to calculate the pKa of a weak acid.
The pH change in a titration can also go the other way around, starting with a strong base and adding an acid.
The Ka expression equals the concentration of H+.
The Ka expression can be simplified by cancelling out the concentration of H+ and the concentration of A-.
The Ka expression can be rewritten as the concentration of H+ times the concentration of A-.
In a titration, the pH change is sharpest when a strong acid and a strong base are used.
The concentration of H+ in a titration is equal to the concentration of A-.
The pH change from H+ ions reacting in full is smallest when a weak acid and a weak base are used in a titration.
The method when nearing the end point is critical, and measurements need to be made from the bottom of the meniscus.
The classic shape of a titration curve is an S-shaped curve.
Titration curves show pH against volume of base added from a titration, with different combinations of weak acids, strong acids, strong bases, and weak bases.
The titration curve starts at pH one when using a strong acid, and rises quickly to a certain point and then becomes basic.
Results need to be recorded to two decimal places and repeated until they are within 0.1 centimeters cubed of each other.
When a strong base is used, the titration curve starts at pH water and rises to a certain point, then becomes basic.
The equivalence point or end point is the point where the acid has been neutralized fully by the base, marked by a sharp vertical rise on the titration curve.
When a weak acid is used, the titration curve starts higher up the curve and doesn't rise as much because a weak base has been used.