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worty [1.4K]
3 years ago
5

Do parts a, b and c

Chemistry
1 answer:
Leona [35]3 years ago
7 0

Answer:- (a)The pH of the buffer solution is 3.90.

(b) the pH of the solution after addition of HCl would be 3.60.

(c) the pH of the buffer solution after addition of NaOH is 4.32.

Solution:- (a) It is a buffer solution so the pH could easily be calculated using Handerson equation:

pH=Pka+log(\frac{base}{acid})

pKa can be calculated from given Ka value as:

pKa=-logKa

pKa=-log(6.3*10^-^5)

pKa = 4.20

let's plug in the values in the Handerson equation:

pH=4.20+log(\frac{0.025}{0.05})

pH = 4.20 - 0.30

pH = 3.90

The pH of the buffer solution is 3.90.

(b) Let's say the acid is represented by HA and the base is represented by A^- .

Original mili moles of HA from part a = 0.05(100) = 5

original mili moles of A^- from part a = 0.025(100) = 2.5

mili moles of HCl that is H^+ added = 0.100(10.0) = 1

This HCl reacts with the base present in the buffer to make HA as:

A^-+H^+\rightarrow HA

Total mili moles of HA after addition of HCl = 5+1 = 6

mili moles of base after addition of HCl = 2.5-1 = 1.5

Let's plug in the values in the Handerson equation again. Here, we could use the mili moles to calculate the pH. The answer remains same even if we use the concentrations also as the final volume is same both for acid and base.

pH=4.20+log(\frac{1.5}{6})

pH = 4.20 - 0.60

pH = 3.60

So, the pH of the solution after addition of HCl would be 3.60.

(c) mili moles of NaOH or OH^- added to the original buffer = 0.05(15.0) = 0.75

This OH^- reacts with HA to form A^- as:

HA+OH^-\rightarrow H_2O+A^-

mili moles of HA after addition of NaOH = 5-0.75 = 4.25

mili moles of A^- after addition of NaOH = 2.5+0.75 = 3.25

Let's plug in the values again in Handerson equation:

pH=4.20+log(\frac{3.25}{4.25})

pH = 4.20 - 0.12

pH = 4.32

So, the pH of the buffer solution after addition of NaOH is 4.32.

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BabaBlast [244]

Answer: 365 K

Explanation:

According to the Arrhenius equation,

K=A\times e^{\frac{-Ea}{RT}}

or,

\log (\frac{K_2}{K_1})=\frac{Ea}{2.303\times R}[\frac{1}{T_1}-\frac{1}{T_2}]

where,

K_1 = rate constant at T_1 = 1.00

K_2 = rate constant at T_2 = 5.00

Ea = activation energy for the reaction = 28.90 kJ/mol= 28900 j/mol

R = gas constant = 8.314 J/mole.K

T_1 = initial temperature = 313 K

T_2 = final temperature = ?

Now put all the given values in this formula, we get

\log (\frac{5.00}{1.00})=\frac{28900}{2.303\times 8.314J/mole.K}[\frac{1}{313K}-\frac{1}{T_2K}]

0.69=\frac{28900}{2.303\times 8.314J/mole.K}[\frac{1}{313K}-\frac{1}{T_2K}]

T_2=365K

Therefore, 365 K is required to increase the reaction rate by 5.00 times.

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If 18 grams of oxygen reacts completely with 4 grams of hydrogen, we would expect how many grams of water? Question 4 options: L
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Answer the following questions about the solubility of AgCl(s). The value of Ksp for AgCl(s) is 1.8 × 10−10.
Firlakuza [10]

Answer:

  • [Ag⁺] = 1.3 × 10⁻⁵M
  • s = 3.3 × 10⁻¹⁰ M
  • Because the common ion effect.

Explanation:

<u></u>

<u>1. Value of [Ag⁺]  in a saturated solution of AgCl in distilled water.</u>

The value of [Ag⁺]  in a saturated solution of AgCl in distilled water is calculated by the dissolution reaction:

  • AgCl(s)    ⇄    Ag⁺ (aq)    +    Cl⁻ (aq)

The ICE (initial, change, equilibrium) table is:

  • AgCl(s)    ⇄    Ag⁺ (aq)    +    Cl⁻ (aq)

I            X                      0                    0

C          -s                      +s                  +s

E         X - s                   s                     s

Since s is very small, X - s is practically equal to X and is a constant, due to which the concentration of the solids do not appear in the Ksp equation.

Thus, the Ksp equation is:

  • Ksp = [Ag⁺] [Cl⁻]
  • Ksp = s × s
  • Ksp = s²

By substitution:

  • 1.8 × 10⁻¹⁰ = s²
  • s = 1.34 × 10⁻⁵M

Rounding to two significant figures:

  • [Ag⁺] = 1.3 × 10⁻⁵M ← answer

<u></u>

<u>2. Molar solubility of AgCl(s) in seawater</u>

Since, the conentration of Cl⁻ in seawater is 0.54 M you must introduce this as the initial concentration in the ECE table.

The new ICE table will be:

  • AgCl(s)    ⇄    Ag⁺ (aq)    +    Cl⁻ (aq)

I            X                      0                  0.54

C          -s                      +s                  +s

E         X - s                   s                     s + 0.54

The new equation for the Ksp equation will be:

  • Ksp = [Ag⁺] [Cl⁻]
  • Ksp = s × ( s + 0.54)
  • Ksp = s² + 0.54s

By substitution:

  • 1.8 × 10⁻¹⁰ = s² + 0.54s
  • s² + 0.54s - 1.8 × 10⁻¹⁰ = 0

Now you must solve a quadratic equation.

Use the quadratic formula:

     

     s=\dfrac{-0.54\pm\sqrt{0.54^2-4(1)(-1.8\times 10^{-10})}}{2(1)}

The positive and valid solution is s = 3.3×10⁻¹⁰ M ← answer

<u>3. Why is AgCl(s) less soluble in seawater than in distilled water.</u>

AgCl(s) is less soluble in seawater than in distilled water because there are some Cl⁻ ions is seawater which shift the equilibrium to the left.

This is known as the common ion effect.

By LeChatelier's principle, you know that an increase in the concentrations of one of the substances that participate in the equilibrium displaces the reaction to the direction that minimizes this efect.

In the case of solubility reactions, this is known as the common ion effect: when the solution contains one of the ions that is formed by the solid reactant, the reaction will proceed in less proportion, i.e. less reactant can be dissolved.

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3 years ago
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