Problem 151
Question
At what concentration of \(\mathrm{CH}_{3} \mathrm{COOH}\) will the \(\left[\mathrm{H}^{+}\right]\) obtained will be same as that obtained from \(10^{-2} \mathrm{M}\) \(\mathrm{HCOOH},\left(\mathrm{Ka}\left(\mathrm{CH}_{3} \mathrm{COOH}\right)=10^{-5}, \mathrm{Ka}(\mathrm{HCOOH})=10^{-4}\right)\) (a) \(10 \mathrm{M}\) (b) \(5 \mathrm{M}\) (c) \(10^{-1} \mathrm{M}\) (d) \(6 \mathrm{M}\)
Step-by-Step Solution
Verified Answer
The concentration of \( \mathrm{CH}_{3} \mathrm{COOH} \) is \( 10^{-1} \mathrm{M} \) (option c).
1Step 1: Understand the Problem
We need to find the concentration of \( \mathrm{CH}_3\mathrm{COOH} \) that results in the same \( [\mathrm{H}^+] \) as that produced by \( 10^{-2} \mathrm{M} \) \( \mathrm{HCOOH} \). We will use the ionization constant \( K_a \) for each acid.
2Step 2: Calculate [H⁺] for HCOOH
For \( \mathrm{HCOOH} \), \( K_a = 10^{-4} \) and initial concentration \([HCOOH]_i = 10^{-2} \mathrm{M} \). We assume that \( x \) is the concentration of \( \mathrm{H}^+ \) dissociated. Thus,\[ K_a = \frac{x^2}{[HCOOH]_i - x} \approx \frac{x^2}{[HCOOH]_i} \] Because \( x \) is small compared to \( [HCOOH]_i \), \( 10^{-4} \approx \frac{x^2}{10^{-2}} \). Solving this, we find\[ x = \sqrt{10^{-4} \times 10^{-2}} = 10^{-3} \mathrm{M} \] So, \( [\mathrm{H}^+] = 10^{-3} \mathrm{M} \).
3Step 3: Set Up the Equation for CH₃COOH
Now we need \([\mathrm{H}^+] = 10^{-3} \) M for \( \mathrm{CH}_3\mathrm{COOH} \) as well. Given \( K_a = 10^{-5} \), if \( c \) is the initial concentration of \( \mathrm{CH}_3\mathrm{COOH} \), we use:\[ K_a = 10^{-5} = \frac{(10^{-3})^2}{c - 10^{-3}} \approx \frac{10^{-6}}{c} \]
4Step 4: Solve for Concentration c
Rearranging the formula, we get\[ 10^{-5}c = 10^{-6} \] \[ c = \frac{10^{-6}}{10^{-5}} = 10^{-1} \mathrm{M} \] Thus, the required concentration of \( \mathrm{CH}_3\mathrm{COOH} \) is \( 10^{-1} \mathrm{M} \).
Key Concepts
Acid Dissociation Constant (Ka)Ionization of Weak AcidsConcentration of Hydrogen IonsFormic Acid Dissociation
Acid Dissociation Constant (Ka)
The acid dissociation constant, commonly represented as \( K_a \), is a crucial parameter illustrating the strength of an acid in aqueous solution. It quantifies the degree of ionization or dissociation of an acid into its hydrogen ion (\( \mathrm{H}^+ \)) and its conjugate base. A higher \( K_a \) value indicates a stronger acid, which dissociates more completely in solution.
For example:
For example:
- Formic acid (HCOOH) has a \( K_a \) of \( 10^{-4} \), indicating a relatively higher degree of ionization compared to acetic acid.
- Acetic acid (CH₃COOH) with a \( K_a \) of \( 10^{-5} \), is weaker since it dissociates less.
Ionization of Weak Acids
Weak acids do not completely ionize in aqueous solutions. Instead, they reach an equilibrium where only a fraction of the acid dissociates into \( \mathrm{H}^+ \) ions and its conjugate base.
The ionization can be expressed as:
\[\text{HA} \rightleftharpoons \mathrm{H}^+ + \mathrm{A}^-\]
For weak acids like acetic and formic acid:
The ionization can be expressed as:
\[\text{HA} \rightleftharpoons \mathrm{H}^+ + \mathrm{A}^-\]
For weak acids like acetic and formic acid:
- The equilibrium position lies towards the left, meaning most acid molecules remain undissociated.
- Calculation of \( [\mathrm{H}^+] \) requires using the \( K_a \) expression: \( K_a = \frac{[\mathrm{H}^+][\mathrm{A}^-]}{[\text{HA}]} \).
Concentration of Hydrogen Ions
The concentration of hydrogen ions, \( [\mathrm{H}^+] \), in solution is a direct measure of the acidity. It is commonly calculated using the formula derived from the ionization constant for weak acids.
Considerations include:
Considerations include:
- For \( 10^{-2} \) M formic acid, we compute \( [\mathrm{H}^+] \) as \( 10^{-3} \) M, using its specific \( K_a \) value.
- To find the corresponding concentration for acetic acid yielding the same \( [\mathrm{H}^+] \), we equate this with its \( K_a \) and solve for its concentration.
Formic Acid Dissociation
Formic acid (HCOOH) dissociates in water to produce\( \mathrm{H}^+ \) ions and its conjugate base, formate ions (\( \mathrm{HCOO}^- \)).
This process is governed by its acid dissociation constant \( (K_a = 10^{-4}) \), reflecting its relative strength as a weak acid.
During dissociation:
This process is governed by its acid dissociation constant \( (K_a = 10^{-4}) \), reflecting its relative strength as a weak acid.
During dissociation:
- The balance of formic acid molecules and ionized forms is maintained dynamically, influencing \( [\mathrm{H}^+] \).
- When fully dissociated, the \( [\mathrm{H}^+] \) can be calculated using the expression \( K_a = \frac{[\mathrm{H}^+][\mathrm{HCOO}^-]}{[ ext{HCOOH}]} \).
Other exercises in this chapter
Problem 148
The solubility product of \(\mathrm{PbI}_{2}\) is \(7.47 \times 10^{-9}\) at \(15^{\circ} \mathrm{C}\) and \(1.39 \times 10^{8}\) at \(25^{\circ} \mathrm{C}\).
View solution Problem 150
The correct order of relative basic strength of the following is (a) \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{O}^{-}>\mathrm{CH} \equiv \mathrm{C}^{-}>-\mathrm{O
View solution Problem 152
When \(\mathrm{NH}_{4} \mathrm{Cl}\) is added to an aqueous solution of \(\mathrm{NH}_{4} \mathrm{OH}\) (a) Conc. of \(\left[\mathrm{OH}^{-}\right]\)ions decrea
View solution Problem 153
\(500 \mathrm{ml}\) of \(0.2 \mathrm{M} \mathrm{HCl}\) is mixed with \(500 \mathrm{ml}\) of \(0.2 \mathrm{M}\) \(\mathrm{CH}_{3} \mathrm{COOH} .25 \mathrm{ml}\)
View solution