Photo AI

A 0.2000 mol L<sup>−1</sup> solution of dichloroacetic acid (CHCl<sub>2</sub>COOH) has a pH of 1.107 - HSC - SSCE Chemistry - Question 35 - 2023 - Paper 1

Question icon

Question 35

A-0.2000-mol-L<sup>−1</sup>-solution-of-dichloroacetic-acid-(CHCl<sub>2</sub>COOH)-has-a-pH-of-1.107-HSC-SSCE Chemistry-Question 35-2023-Paper 1.png

A 0.2000 mol L<sup>−1</sup> solution of dichloroacetic acid (CHCl<sub>2</sub>COOH) has a pH of 1.107. Dichloroacetic acid is monoprotic. Calculate the K<sub>a</sub>... show full transcript

Worked Solution & Example Answer:A 0.2000 mol L<sup>−1</sup> solution of dichloroacetic acid (CHCl<sub>2</sub>COOH) has a pH of 1.107 - HSC - SSCE Chemistry - Question 35 - 2023 - Paper 1

Step 1

Calculate K<sub>a</sub> for dichloroacetic acid

96%

114 rated

Answer

To find the ionization constant K<sub>a</sub> for dichloroacetic acid, we first need to determine the concentration of hydrogen ions [H<sup>+</sup>] provided by the pH.

Using the formula:

[H+]=10pH=101.107=0.0782 mol L1[H^+] = 10^{-pH} = 10^{-1.107} = 0.0782 \text{ mol L}^{-1}

Next, we can set up the equilibrium expression for the dissociation of dichloroacetic acid:

[ \text{CHCl}_2\text{COOH}(aq) \rightleftharpoons \text{H}^+(aq) + \text{CHCl}_2\text{COO}^-(aq) ]

We can create a table for the solution:

SpeciesInitial (mol L<sup>−1</sup>)Change (mol L<sup>−1</sup>)Equilibrium (mol L<sup>−1</sup>)
CHCl<sub>2</sub>COOH0.2000-0.07820.1218
H<sup>+</sup>0+0.07820.0782
CHCl<sub>2</sub>COO<sup></sup>0+0.07820.0782

Now, we can substitute these values into the K<sub>a</sub> equation:

Ka=[H+][CHCl2COO][CHCl2COOH]=(0.0782)(0.0782)0.1218K_a = \frac{[H^+][CHCl_2COO^-]}{[CHCl_2COOH]} = \frac{(0.0782)(0.0782)}{0.1218}

Calculating this gives:

Ka=0.0501K_a = 0.0501

Step 2

Explain the relative strength of CH<sub>3</sub>COOH and CCl<sub>3</sub>COOH

99%

104 rated

Answer

The pK<sub>a</sub> of trichloroacetic acid is lower than the pK<sub>a</sub> of acetic acid, indicating that trichloroacetic acid is a stronger acid than acetic acid.

A significant factor that contributes to this is the ΔS<sup>°</sup> data: both acids have different entropy changes, which affects their Gibbs free energy (ΔG<sup>°</sup>). The ΔG<sup>°</sup> values show that trichloroacetic acid has a much more favorable dissociation compared to acetic acid.

Furthermore, the strong electron-withdrawing effect of the three chlorine atoms in trichloroacetic acid stabilizes the negative charge on the conjugate base (CCl<sub>3</sub)COO<sup></sup>, making it a much stronger acid compared to CH<sub>3</sub>COOH, which has a less effective electron-withdrawing structure.

Join the SSCE students using SimpleStudy...

97% of Students

Report Improved Results

98% of Students

Recommend to friends

100,000+

Students Supported

1 Million+

Questions answered

;