A) CH3CH2COOH (aq) + NaOH (aq) CH3CH2COONa (aq) + H2O (l)
B) pH of solution before addition of any NaOH.
Initially there is only CH3CH2COOH present in the solution, hence pH of solution will be due to dissociation of CH3CH2COOH.
Consider a dissociation of CH3CH2COOH in water.
CH3CH2COOH (aq) + H2O (l) CH3CH2COO -(aq) + H3O +(aq)
For above reaction, dissociation constant is Ka = [CH3CH2COO - ] [H3O + ] / [CH3CH2COOH ]
Let's use ICE table.
Concentration (M) | CH3CH2COOH | CH3CH2COO - | H3O + |
Initial | 0.01 | ||
Change | - X | +X | +X |
Equilibrium | 0.01 - X | X |
X |
Therefore, K a = ( X) (X) / 0.01 - X = 10 -4.87 = 1.349 10 -05
X 2 / 0.01 - X = 1.349 10 -05
CH3CH2COOH is a weak acid. Hence, we can assume X is very small as compared to 0.01 Hence we can write 0.01- X 0.01.
X 2 / 0.01 = 1.349 10 -05
X 2 = 0.01 (1.349 10 -05 )
X 2 = 1.349 10 -07
X = 3.673 10 -04 = [CH3CH2COO - ] = [H3O + ]
We have, pH = - log [H3O + ]
pH = - log 3.673 10 -04 = 3.43
ANSWER : pH of solution before addition of any NaOH = 3.43
C) Calculation of volume of NaOH required to reach equivalence point
Consider reaction, CH3CH2COOH (aq) + NaOH (aq) CH3CH2COONa (aq) + H2O (l)
We have, M acid V acid = M base V base
V base = M acid V acid / M base
V base = 0.01 M 20 ml / 0.05 M
V base = 4.0 ml
Volume of NaOH required to reach equivalence point = 4.0 ml
D) pH of solution at equivalence point ( 4.0 ml)
At equivalence point, all CH3CH2COOH is consumed by added NaOH. pH of solution will be due to dissociation of CH3CH2COOH in water.
CH3CH2COO- (aq) + H2O (l) CH3CH2COOH (aq) + OH -(aq)
For above reaction, dissociation constant is Kb = [CH3CH2COOH] [OH - ] / [CH3CH2COO- ]= Kw / Ka
K b = 10 -14 / 1.349 x 10 -05 = 7.413 x 10 -10
mmol of CH3CH2COONa produced = mmol of NaOH added to the solution = 0.05 4.0 = 0.2 mmol
Volume of the solution = volume of CH3CH2COOH + volume of NaOH = 20 ml + 4.0 = 24.0 ml
[CH3CH2COONa] = No. of moles of CH3CH2COONa / volume of solution in L
= [ 0.2 /1000] /[ 24.0 /1000]
=0.00833 M
Let's use ICE table.
Concentration (M) | CH3CH2COO - | CH3CH2COOH | OH - |
Initial | 0.00833 | ||
Change | - X | +X | +X |
Equilibrium | 0.00833 - X | X |
X |
Therefore, K b = (X) (X) / 0.00833 - X
K b = X 2 / 0.00833 - X = 7.413 x 10 -10
Here X is very small as compared to 0.00833. Hence we can write 0.00833 - X 0.00833.
X 2 / 0.00833 = 7.413 x 10 -10
X 2 = 0.00833 ( 7.413 x 10 -10 )
X 2 = 6.175 x 10 -12
X = 2.485 x 10 -06 M = [CH3CH2COOH] = [OH - ]
We have relation, [H +] [OH - ] = 10 -14
[H + ] = 10 -14 / [OH - ] = 10 -14 / 2.485 x 10 -06 =4.024 x 10 -09 M
We have, pH = - log [H + ] = - log 4.024 x 10 -09 = 8.40
D) pH of solution at half equivalence point.
At half equivalence point, half quantity of acid will be converted into its salt i e at this stage solution contain weak acid and it's salt, Hence this solution acts as a buffer and it's pH is calculated by using Henderson's equation.
pH = pKa + log [Salt] /[ Acid]
pH = 4.87 + log [CH3CH2COONa] / [CH3CH2COOH]
We have, [CH3CH2COOH]= [CH3CH2COONa]
pH = 4.87 + log 1
pH = 4.87 + 0
pH = 4.87
E)
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