In water, strong acids completely dissociate into free protons and their conjugate base.
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Key TakeawaysKey PointsStrong acids can catalyze chemical reactions.Strong acids are defined by their pKa. The acid must be stronger in aqueous solution than a hydronium ion, so its pKa must be lower than that of a hydronium ion. Therefore, strong acids have a pKa of Strong acids can be organic or inorganic.Strong acids must be handled carefully because they can cause severe chemical burns.Strong acids are essential for catalyzing some reactions, including the synthesis and hydrolysis of carbonyl compounds.Key Termscarbonyl: a divalent functional group (-CO-), characteristic of aldehydes, ketones, carboxylic acids, amides, carboxylic acid anhydrides, carbonyl halides, esters, and others.ester: a compound usually formed by condensing an alcohol and an acid and eliminating of water. it contains the functional group carbon-oxygen double bond joined via carbon to another oxygen atomhydrolysis: a chemical process of decomposition; involves splitting a bond and adding the hydrogen cation and water’s hydroxide anion
Definition of Strong Acids
The strength of an acid refers to the ease with which the acid loses a proton. A strong acid ionizes completely in an aqueous solution by losing one proton, according to the following equation:
where HA is a protonated acid, H+ is the free acidic proton, and A– is the conjugate base. Strong acids yield weak conjugate bases. For sulfuric acid, which is diprotic, the “strong acid” designation refers only to the dissociation of the first proton:
More precisely, the acid must be stronger in aqueous solution than a hydronium ion (H+), so strong acids have a pKa
Ionization of acids and bases in water: A strong acid ionizes completely in an aqueous solution by losing one proton (H+).
Due to the complete dissociation of strong acids in aqueous solution, the concentration of hydronium ions in the water is equal to the total concentration (ionized and un-ionized) of the acid introduced to solution:
Strong acids, like strong bases, can cause chemical burns when exposed to living tissue.
Examples of Strong Acids
Some common strong acids (acids with pKa Hydroiodic acid (HI): pKa = -9.3Hydrobromic acid (HBr): pKa = -8.7Perchloric acid (HClO4): pKa ≈ -8Hydrochloric acid (HCl): pKa = -6.3Sulfuric acid (H2SO4): pKa1 ≈ -3 (first dissociation only)p-Toluenesulfonic acid: pKa = -2.8Nitric acid (HNO3): pKa ≈ -1.4Chloric acid (HClO3): pKa ≈ 1.0
p-Toluenesolfonic acid: p-Toluenesulfonic acid is an example of an organic soluble strong acid, with a pKa of -2.8.
Strong Acid Catalysis
Strong acids can accelerate the rate of certain reactions. For instance, strong acids can accelerate the synthesis and hydrolysis of carbonyl compounds. With carbonyl compounds such as esters, synthesis and hydrolysis go through a tetrahedral transition state, where the central carbon has an oxygen, an alcohol group, and the original alkyl group. Strong acids protonate the carbonyl, which makes the oxygen positively charged so that it can easily receive the double-bond electrons when the alcohol attacks the carbonyl carbon; this enables ester synthesis and hydrolysis.
A weak acid only partially dissociates in solution.
Key TakeawaysKey PointsThe dissociation of weak acids, which are the most popular type of acid, can be calculated mathematically and applied in experimental work.If the concentration and Ka of a weak acid are known, the pH of the entire solution can be calculated. The exact method of calculation varies according to what assumptions and simplifications can be made.Weak acids and weak bases are essential for preparing buffer solutions, which have important experimental uses.Key Termsconjugate acid: the species created when a base accepts a protonconjugate base: the species created after donating a proton.weak acid: one that dissociates incompletely, donating only some of its hydrogen ions into solution
Vinegars: All vinegars contain acetic acid, a common weak acid.
Weak acids ionize in a water solution only to a very moderate extent. The generalized dissociation reaction is given by:
where HA is the undissociated species and A– is the conjugate base of the acid. The strength of a weak acid is represented as either an equilibrium constant or a percent dissociation. The equilibrium concentrations of reactants and products are related by the acid dissociation constant expression, Ka:
The greater the value of Ka, the more favored the H+ formation, which makes the solution more acidic; therefore, a high Ka value indicates a lower pH for a solution. The Ka of weak acids varies between 1.8×10−16 and 55.5. Acids with a Ka less than 1.8×10−16 are weaker acids than water.
If acids are polyprotic, each proton will have a unique Ka. For example, H2CO3 has two Ka values because it has two acidic protons. The first Ka refers to the first dissociation step:
This Ka value is 4.46×10−7 (pKa1 = 6.351). The second Ka is 4.69×10−11 (pKa2 = 10.329) and refers to the second dissociation step:
Calculating the pH of a Weak Acid Solution
The Ka of acetic acid is
In this case, you can find the pH by solving for concentration of H+ (x) using the acid’s concentration (F) and Ka. Assume that the concentration of H+ in this simple case is equal to the concentration of A–, since the two dissociate in a 1:1 mole ratio:
This quadratic equation can be manipulated and solved. A common assumption is that x is small; we can justify assuming this for calculations involving weak acids and bases, because we know that these compounds only dissociate to a very small extent. Therefore, our above equation simplifies to:
Although it is only a weak acid, a concentrated enough solution of acetic acid can still be quite acidic.
Calculating Percent Dissociation
Percent dissociation represents an acid’s strength and can be calculated using the Ka value and the solution’s pH.
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