The pKa of bromoacetic acid is approximately 2.64.
The pKa value of benzoic acid is approximately 4.2.
The pKa of fluoroacetic acid is approximately 2.7. It is a weak acid with a dissociation constant similar to acetic acid.
Formic acid is stronger than nitrous acid. This is because formic acid is a stronger acid with a lower pKa value compared to nitrous acid. The lower the pKa value, the stronger the acid.
The pKa of an acid is calculated by taking the negative logarithm (base 10) of the acid dissociation constant (Ka). In this case, the pKa would be approximately 5.19.
Cholic acid is a bile acid, a white crystalline substance insoluble in water, with a pKa of about 5.5. Urea is an organic compound with the chemical formula (NH2)2CO often found in the urine of animals, with a pKa of about 0.18.
Salicylic acid has a pKa of 1.96 and acetylsalicylic acid (Aspirin) has a pKa of 3.48. Therefore salicylic acid is the stronger acid.
The pKa of chlorosulfonic acid is approximately -6.3. It is a very strong acid due to the electronegativity of the chlorine and sulfur atoms, making it highly acidic.
It refers to the acidity of the fatty acid (which make up the oils). Every fatty acid is composed of a non-polar long chain of hydrocarbons (carbon and hydrogen) and a polar head made up of Carboxylic ACID. Every acid has something called pKa which determines the acidity of that acid.The bigger the pKa (e.g. 25), the weaker the acid.The smaller ther pKa (e.g. 2), the stronger the acid.
HCl is a stronger acid than H2SO3. HCl is a strong acid that completely dissociates in water to release H+ ions, while H2SO3 is a weak acid that only partially dissociates to release H+ ions.
Carbonic acid is stronger than vinegar. Vinegar is mainly acetic acid dissolved in water, whereas carbonic acid is formed when carbon dioxide dissolves in water. Carbonic acid is a weak acid but is stronger than acetic acid.
Ethers do not have a defined pKa value because they do not contain any protons that can be donated or accepted in an acid-base reaction. Therefore, ethers are considered to be neutral compounds.
pKa = -log KapKa = -log 5.4x10^-10pKa = 9.27
There are two answers: bicarbonate has two pKa's - because bicarbonate can gain a proton to become carbonic acid or lose a proton to become carbonate. Two reactions; two pKa's. The pKa for bicarbonate carbonic acid reaction is 6.4 The pKa for bicarbonate carbonate reaction is 10.3 Both pKa's are temperature sensitive.
By definition, the pKa of a weak acid is the pH at which the concentrations of the acid and its conjugate base are equal. In this case, since the solution is yellow (acid) and blue (base) at pH 4.68, it means that the concentration of the acid and base forms of the indicator are equal. Therefore, the pKa of bromcresol green is 4.68.
The pKa of mandelic acid is around 3.4 for the carboxylic acid group and around 9.8 for the phenolic hydroxyl group. This means that mandelic acid is a weak acid, with the carboxylic acid group being more acidic than the phenolic hydroxyl group.
The pKa of fluoroacetic acid is approximately 2.7. It is a weak acid with a dissociation constant similar to acetic acid.
The pKa value for sodium hydride (NaH) is approximately 36. This means that NaH is a very strong base that readily donates a proton in a reaction.