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ycow [4]
2 years ago
15

A 0.50 M solution of formic acid, HCOOH, has a pH of 2.02. Calculate the percent ionization of HCOOH

Chemistry
2 answers:
kirza4 [7]2 years ago
8 0

Answer is: <span>the percent ionizationof formic acid is 1,82%.
Chemical reaction: HCOOH(aq) </span>⇄ H⁺(aq) + HCOO⁻(aq).<span>
pKa(</span>HCOOH) = 3,77.

Ka(HCOOH) = 1,7·10⁻⁴.

c(HCOOH) = 0,5 M.

<span> [H</span>⁺] = [HCOO⁻] = x; equilibrium concentration.<span>
[HA] = 0,1 M - x.
Ka = [H</span>⁺] · [HCOO⁻] / [HCOOH].<span>
0,00017 = x² / 0,5 M - x.
Solve quadratic equation: x = 0,0091 M.
α = 0,0091 M ÷ 0,5 M · 100% = 1,82%.</span>

Stolb23 [73]2 years ago
8 0

Answer : 1.91 %

Explanation : The steps to solve this problem are explained below;

1.  HCOOH ⇄ HCOO^{-} + H^{+}      

Here Ka =([HCOO^{-}]_{eq} X  [H^{+}]_{eq} )/  [HCOOH]_{eq}                                                        

As the equilibrium concentration of H^{+} will be the pH of the solution.

∴ [H^{+}]_{eq} = 10^{(-2.02)} = 9.55 x [tex] 10^{-3} M  

2. The initial concentration of HCOOH.  When it loses x moles from it as the acid undergoes dissociation to form HCOO^{-} and H^{+}.  

3.  The moles present will be as

         [HCOOH] (M)                 [H^{+}](M)           [HCOO^{-}](M)  

Initial       0.50                                0.00                                          0.00


After Change  -x                              +x                                            +x


Equilibrium      ( 0.50 -x)                     x                                              x



∴ Ka   =   (x) x (x)  / (0.50 - x)  

4.  Assuming that all of the H^{+} comes from the acid, and none from water.  

As [H^{+}]_{eq} = 9.55 x10^{-3} which is much higher than the 1.0 x10^{-7 } M [tex[H^{+}[/tex] from water.  

Also, the concentration of HCOOH will change very little, from 0.50  to 0.50 - 9.55 x 10^{-3}.  

The change in concentration can be ignored if it is less than 5% of the original concentration.  

∴ 0.50 M x 5% = 0.025, so the change in [HCOOH] in this problem can be ignored.    

Now,  Ka = (x)(x)/0.50 = (9.55 x 10^{-3})^{2} /0.50= 1.82 x 10^{-4}


Now, calculating the percent ionization for this problem.  

which will represent the relative number of acid molecules which dissociate. It is calculated as :


[H^{+}]_{eq} x  100 /[HCOOH]_{i}                                                        

∴ percent ionization = {(9.55 x 10^{-3})/ (0.50)}x 100 = 1.91 %


This value of 1.91 % indicates that very little of this acid dissociates (ionizes) under these conditions.  

For strong acids and bases, the percent ionization is 100%.

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Write a balanced half-reaction for the oxidation of liquid water H2O to aqueous hydrogen peroxide H2O2 in basic aqueous solution
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Answer : The balanced half-reaction in a basic solution will be,

2OH^-(aq)\rightarrow H_2O_2(aq)+2e^-  

Explanation :

Redox reaction or Oxidation-reduction reaction : It is defined as the reaction in which the oxidation and reduction reaction takes place simultaneously.

Rules for the balanced chemical equation in basic solution are :

First we have to write into the two half-reactions.

Now balance the main atoms in the reaction.

Now balance the hydrogen and oxygen atoms on both the sides of the reaction.

If the oxygen atoms are not balanced on both the sides then adding water molecules at that side where the more number of oxygen are present.

If the hydrogen atoms are not balanced on both the sides then adding hydroxide ion (OH^-) at that side where the less number of hydrogen are present.

Now balance the charge.

  • The half reaction is :

H_2O(l)\rightarrow H_2O_2(aq)

  • Now balance the oxygen atoms.

H_2O(l)\rightarrow H_2O_2(aq)+H_2O(l)

  • Now balance the hydrogen atoms.

H_2O(l)+2OH^-(aq)\rightarrow H_2O_2(aq)+H_2O(l)

  • Now balance the charge.

H_2O(l)+2OH^-(aq)\rightarrow H_2O_2(aq)+H_2O(l)+2e^-

The balanced half-reaction in a basic solution will be,

2OH^-(aq)\rightarrow H_2O_2(aq)+2e^-

7 0
2 years ago
Two weak acids, A and B, have pKa values of 4 and 6, respectively. Which statement is true?A) Acid A dissociates to a greater ex
zalisa [80]

Answer:

A) Acid A dissociates to a greater extent in water than acid B

Explanation:

A) Acid A dissociates to a greater extent in water than acid B

We are given the pKa for both acids, and we know

pKa = - log Ka

Taking antilog to both sides of the equation we can solve for Ka

⇒ -pKa = log Ka

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10 ^-pka = Ka

So ka for acid A = 10⁻⁴

and

ka for acid B = 10⁻⁶

True the equilibrium constant for acid A is greater, so it dissociates more.

B) For solutions of equal concentration, acid B will have a lower pH.

We know the stronger acid is A, and it dissociates more. Since pH is the negative log of H₃O⁺ concentration, it follows that at equal concentrations the acid A will have at equilibrium a greater [H₃O⁺] and hence a lower pH

C) B is the conjugate base of A

False:

If B were the conjugate base of A, its  Kb would have been given by:

Ka x Kb = Kw

Kb = 10⁻¹⁴/10⁻⁶ = 10⁻⁸ for the conjugate base of acid B

Kb = 10⁻¹⁴/10⁻⁴ = 10⁻¹⁰ for the conjugate base of acid A

which are not equal.

D) Acid A is more likely to be a polyprotic acid than acid B.

False

Just having the pkas for both acids one cannot know if any of the acids is polyprotic. We will need the formula for the acids.

E) The equivalence point of acid A is higher than that of acid B

False

The equivalence point depends on the the concentration of the acids  and their volumes.

The equivalence point is reached in the titration when the number of equivalents of base equals the number of equivalents of acid:

# equivalents acid = # equivalents of base  @ end point

and

# equivalents acid = Molarity of acid x Volume of acid

4 0
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