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[c] [2] For example, a hypothetical weak acid having K a = 10 −5, the value of log K a is the exponent (−5), giving pK a = 5. For acetic acid, K a = 1.8 x 10 −5, so pK a is 4.7. A higher K a corresponds to a stronger acid (an acid that is more dissociated at equilibrium).
The Henderson–Hasselbalch equation can be used to model these equilibria. It is important to maintain this pH of 7.4 to ensure enzymes are able to work optimally. [10] Life threatening Acidosis (a low blood pH resulting in nausea, headaches, and even coma, and convulsions) is due to a lack of functioning of enzymes at a low pH. [10]
This equation shows that the pH of a solution of a weak acid depends on both its value and its concentration. Typical examples of weak acids include acetic acid and phosphorous acid . An acid such as oxalic acid ( HOOC − COOH {\displaystyle {\ce {HOOC-COOH}}} ) is said to be dibasic because it can lose two protons and react with two molecules ...
A plot of the common logarithm of the reaction rate constant k versus the logarithm of the ionization constant K a for a series of acids (for example a group of substituted phenols or carboxylic acids) gives a straight line with slope α and intercept C. The Brønsted equation is a free-energy relationship.
In chemistry, biochemistry, and pharmacology, a dissociation constant (K D) is a specific type of equilibrium constant that measures the propensity of a larger object to separate (dissociate) reversibly into smaller components, as when a complex falls apart into its component molecules, or when a salt splits up into its component ions.
For example, carbonic acid: H 2 CO 3 (l) + H 2 O (l) ⇌ HCO 3 − (aq) + H 3 O + (aq) . The concentrations of reactants and products in an equilibrium mixture are determined by the analytical concentrations of the reagents (A and B or C and D) and the equilibrium constant , K .
The Charlot equation, named after Gaston Charlot, is used in analytical chemistry to relate the hydrogen ion concentration, and therefore the pH, with the formal analytical concentration of an acid and its conjugate base. It can be used for computing the pH of buffer solutions when the approximations of the Henderson–Hasselbalch equation ...
For example, in ammonium chloride solution, NH + 4 is the main influence for acidic solution. It has greater K a value compared to that of water molecules; K a of NH + 4 is 5.6 × 10 −10, and K w of H 2 O is 1.0 × 10 −14. This ensures its deprotonation when reacting with water, and is responsible for the pH below 7 at room temperature.