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DanielleElmas [232]
3 years ago
9

which process describe water changing from a liquid state to a gas? condensation evaporation infiltration precipitation

Chemistry
2 answers:
Bogdan [553]3 years ago
8 0
<span>evaporation  is the process that describe changing of water from liquid to gas</span>
ValentinkaMS [17]3 years ago
8 0

Answer: Option (b) is the correct answer.

Explanation:

When we heat a liquid substance then its molecules gain kinetic energy due to which more number of collisions occur between the particles. As a result, liquid state of substance will change into gaseous state.

This process of conversion of liquid into gaseous phase is known as evaporation.

Whereas when gaseous phase changes into liquid state then there occurs decrease in kinetic energy of molecules of a substance. Due to which they change into liquid state. This process is known as condensation.

When two aqueous solution react chemically with each other then an insoluble solid formation into the solution is known as precipitate. This type of reaction is known as precipitation.

When water present on the surface of earth enters into the soil then it is known as infiltration.

Therefore, we can conclude that evaporation process describe water changing from a liquid state to a gas.

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) Given the following balanced equation, determine the rate of reaction with respect to [O2]. If the rate of formation of O2is 7
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Answer:

Rate of the reaction is 0.2593 M/s

-0.5186 M/s is the rate of the loss of ozone.

Explanation:

The rate of the reaction is defined as change in any one of the concentration of reactant or product per unit time.

2O_3\rightleftharpoons 3O_2

Rate of formation of oxygen : 7.78\times 10^{-1} M/s

Rate of the reaction(R) =\frac{-1}{2}\frac{d[O_3]}{dt}=\frac{1}{3}\frac{d[O_2]}{dt}

R=\frac{1}{3}\frac{d[O_2]}{dt}

Rate of formation of oxygen=3 × (R)

7.78\times 10^{-1} M/s=3\times R

Rate of the reaction(R): 0.2593 M/s

Rate of the reaction is 0.2593 M/s

Rate of disappearance of the ozone:

R=-\frac{1}{2}\frac{d[O_3]}{dt}

\frac{d[O_3]}{dt}=-2\times R=-2\times 0.2593\times M/s=-0.5186M/s

-0.5186 M/s is the rate of the loss of ozone.

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A 50.0 mL solution of 0.129 M KOH is titrated with 0.258 M HCl. Calculate the pH of the solution after the addition of each of t
kobusy [5.1K]

Answer:

A- pH = 13.12

B- pH = 12.91

C- pH = 12.71

D- pH = 12.43

E- pH = 11.55

F- pH = 7

G- pH = 2.46

H- pH = 1.88

Explanation:

This is a titration of a strong base with a strong acid. The neutralization reaction is: KOH (aq) + HCl (aq) →  H₂O(l) + KCl(aq)

Our pH at the equivalence point is 7, because we have made a neutral salt.

To determine the volume at that point we state the formula for titration:

mmoles of base = mmoles of acid

Volume of base  . M of base = Volume of acid . M of acid

50mL . 0.129M = 0.258 M . Volume of acid

Volume of acid = (50mL . 0.129M) / 0.258 M →  25 mL (Point <u>F</u>)

When we add 25 mL of HCl, our pH will be 7.

A- At 0 mL of acid, we only have base.

KOH → K⁺ + OH⁻

[OH⁻] = 0.129 M

To make more easy the operations we will use, mmol.

mol . 1000 = mmoles → mmoles / mL = M

- log 0.129 = 0.889

14 - 0.889 = 13.12

B-  In this case we are adding, (7 mL . 0.258M) = 1.81 mmoles of H⁺

Initially we have  0.129 M . 50 mL = 6.45 mmoles of OH⁻

1.81 mmoles of H⁺ will neutralize, the 6.45 mmoles of OH⁻ so:

6.45 mmol - 1.81 = 4.64 mmoles of OH⁻

This mmoles of OH⁻ are not at 50 mL anymore, because our volume has changed. (Now, we have 50 mL of base + 7 mL of acid) = 57 mL of total volume.

[OH⁻] = 4.64 mmoles / 57 mL = 0.0815 M

- log 0.0815 M = 1.09 → pOH

pH = 14 - pOH → 14 - 1.09 = 12.91

C- In this case we add (12.5 mL . 0.258M) = 3.22 mmoles of H⁺

<em>Our initial mmoles of OH⁻ would not change through all the titration. </em>

Then 6.45 mmoles of OH⁻ are neutralized by 3.22 mmoles of H⁺.

6.45 mmoles of OH⁻ - 3.22 mmoles of H⁺ = 3.23 mmoles of OH⁻

Total volume is: 50 mL of base + 12.5 mL = 62.5 mL

[OH⁻] = 3.23 mmol / 62.5 mL = 0.0517 M

- log  0.0517 = 1.29 → pOH

14 - 1.11 = 12.71

D- We add (18 mL . 0.258M) = 4.64 mmoles of H⁺

6.45 mmoles of OH⁻ are neutralized by 4.64 mmoles of H⁺.

6.45 mmoles of OH⁻ - 4.64 mmoles of H⁺ = 1.81 mmoles of OH⁻

Total volume is: 50 mL of base + 18 mL = 68 mL

[OH⁻] = 1.81 mmol / 68 mL = 0.0265 M

- log  0.0265 = 1.57 → pOH

14 - 1.57 = 12.43

E- We add (24 mL . 0.258M) = 6.19 mmoles of H⁺

6.45 mmoles of OH⁻ are neutralized by 6.19 mmoles of H⁺.

6.45 mmoles of OH⁻ - 6.19 mmoles of H⁺ = 0.26 mmoles of OH⁻

Total volume is: 50 mL of base + 24 mL = 74 mL

[OH⁻] = 0.26 mmol / 74 mL = 3.51×10⁻³ M

- log  3.51×10⁻³  = 2.45 → pOH

14 - 2.45 = 11.55

F- This the equivalence point.

mmoles of OH⁻ = mmoles of H⁺

We add (25 mL . 0.258M) = 6.45 mmoles of H⁺

All the OH⁻ are neutralized.

OH⁻  +  H⁺  ⇄   H₂O              Kw

[OH⁻] = √1×10⁻¹⁴   →  1×10⁻⁷  →  pOH = 7

pH → 14 - 7 = 7

G- In this case we have an excess of H⁻

We add (26 mL . 0.258M ) = 6.71 mmoles of H⁺

We neutralized all the OH⁻ but some H⁺ remain after the equilibrium

6.71 mmoles of H⁺ - 6.45 mmoles of OH⁻ = 0.26 mmoles of H⁺

[H⁺] = 0.26 mmol / Total volume

Total volume is: 50 mL + 26 mL → 76 mL

[H⁺] = 0.26 mmol / 76 mL → 3.42×10⁻³ M

- log 3.42×10⁻³ = 2.46 → pH

H- Now we add (29 mL . 0.258M) = 7.48 mmoles of H⁺

We neutralized all the OH⁻ but some H⁺ remain after the equilibrium

7.48 mmoles of H⁺ - 6.45 mmoles of OH⁻ = 1.03 mmoles of protons

Total volume is 50 mL + 29 mL = 79 mL

[H⁺] = 1.03 mmol / 79 mL → 0.0130 M

- log 0.0130 = 1.88 → pH

After equivalence point, pH will be totally acid, because we always have an excess of protons. Before the equivalence point, pH is basic, because we still have OH⁻ and these hydroxides, will be neutralized through the titration, as we add acid.

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