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Zina [86]
2 years ago
5

The pH of 1M MOH solution which is only 10% dissociated.

Chemistry
2 answers:
GaryK [48]2 years ago
7 0

Answer:

asgen

Explanation:

mylen [45]2 years ago
7 0

Answer:

13

Explanation:

1M MOH solution dissociates into 0.1M OH- ions.

pOH= -log(OH-)

       =    1

pH=14-1

    =13

You might be interested in
How many liters of 3.0 M NaOH solution will react with 2.4 mol H2SO4? (Remember to balance the equation.)
timurjin [86]

Answer:

1.6 L is the volume of NaOH that has reacted

Explanation:

The balanced reaction is:

H₂SO₄ + 2NaOH → Na₂SO₄  + 2H₂O

This is a neutralization reaction between a strong acid and a strong base. The products are the correspond salt and water.

We propose this rule of three:

1 mol of sulfuric acid needs 2 mol of NaOH to react to react

Then, 2.4 moles of H₂SO₄  will react with (2.4 . 2) / 1 = 4.8 moles of NaOH

As molarity is 3M, we can determine the volume of our solution

Molarity (M) = mol / volume(L) → Volume(L) = mol / Molarity

Volume(L) = 4.8 mol / 3 M = 1.6 L

3 0
2 years ago
Which best describes the motion of pentane molecules in liquid phase?
Ganezh [65]
Hydrocarbons may vary from state to state depending on the length of the carbon chain. For methane to butane, they are usually in gas form. Starting from pentane, they are in the liquid form. For very long carbon chains, that occur as solids. Now, it depends if the pentane is in a nonpolar liquid or polar liquid. Since pentane is nonpolar, it is miscible in the liquid solvent. The movements would most likely be free flowing. But if he solvent is polar, the molecules would repel with one another. In the end, it will form two liquid phases, on for the pentane and one for the polar solvent.
3 0
2 years ago
A 7.591-9 gaseous mixture contains methane (CH4) and butane
mestny [16]

Answer:

65.71%

Explanation:

First, we can write the mass of the mixture, thus:

7.519g = X + Y <em>(1)</em>

<em>Where X is the mass of methane and Y the mass of butane</em>

<em />

Also, the reactions of combustion are:

CH₄ + 2O₂ → CO₂ + 2H₂O

<em>2 moles of oxygen react per mole of methane</em>

C₄H₁₀ + 13/2 O₂ → 4CO₂ + 5H₂O

<em>13/2 moles of oxygen react per mole of methane</em>

<em />

That means, in therms of moles of oxygen we can write:

0.9050 moles = 2X/16.04 + 13/2Y/ 58.12

0.9050 = 0.12469X + 0.11184Y <em>(2)</em>

<em>Where 16.04 and 58.12 are molar masses of methane and butane</em>

That is because if X is the mass of methane:

X g Methane * (1mol / 16.04g) = Moles methane

Moles methane * (2 moles Oxygen / mole methane) = Moles oxygen

Replacing (1) in (2):

0.9050 = 0.12469X + 0.11184 (7.519 - X)

0.9050 = 0.12469X + 0.841 - 0.11184X

0.0641 = 0.01285X

X = 4.988g = Mass of methane.

And mass percent of methane is:

4.988g / 7.591g * 100

<h3>65.71%</h3>

7 0
2 years ago
Consider a general reaction A ( aq ) enzyme ⇌ B ( aq ) A(aq)⇌enzymeB(aq) The Δ G ° ′ ΔG°′ of the reaction is − 5.980 kJ ⋅ mol −
Grace [21]

Answer : The value of K_{eq} is, 11.2

The value of \Delta G_{rxn} is -9.04 kJ/mol

Explanation :

The relation between the equilibrium constant and standard Gibbs free energy is:

\Delta G^o=-RT\times \ln K_{eq}

where,

\Delta G^o = standard Gibbs free energy  = -5.980 kJ/mol = -5980 J/mol

R = gas constant = 8.314 J/K.mol

T = temperature = 25^oC=273+25=298K

K_{eq}  = equilibrium constant  = ?

Now put all the given values in the above formula, we get:

\Delta G^o=-RT\times \ln K_{eq}

-5980J/mol=-(8.314J/K.mol)\times (298K)\times \ln K_{eq}

K_{eq}=11.2

Thus, the value of K_{eq} is, 11.2

Now we have to calculate the \Delta G_{rxn}.

The formula used for \Delta G_{rxn} is:

The given reaction is:

A(aq)\rightleftharpoons B(aq)

\Delta G_{rxn}=\Delta G^o+RT\ln Q

\Delta G_{rxn}=\Delta G^o+RT\ln \frac{[B]}{[A]}    ............(1)

where,

\Delta G_{rxn} = Gibbs free energy for the reaction  = ?

\Delta G_^o =  standard Gibbs free energy  = -30.5 kJ/mol

R = gas constant = 8.314\times 10^{-3}kJ/mole.K

T = temperature = 37.0^oC=273+37.0=310K

Q = reaction quotient

[A] = concentration of A = 1.8 M

[B] = concentration of B = 0.55 M

Now put all the given values in the above formula 1, we get:

\Delta G_{rxn}=(-5980J/mol)+[(8.314J/mole.K)\times (310K)\times \ln (\frac{0.55}{1.8})

\Delta G_{rxn}=-9035.75J/mol=-9.04kJ/mol

Therefore, the value of \Delta G_{rxn} is -9.04 kJ/mol

3 0
2 years ago
Ammonia gas is compressed from 21°C and 200 kPa to 1000 kPa in an adiabatic compressor with an efficiency of 0.82. Estimate the
Evgen [1.6K]

Explanation:

It is known that efficiency is denoted by \eta.

The given data is as follows.

     \eta = 0.82,       T_{1} = (21 + 273) K = 294 K

     P_{1} = 200 kPa,     P_{2} = 1000 kPa

Therefore, calculate the final temperature as follows.

         \eta = \frac{T_{2} - T_{1}}{T_{2}}    

         0.82 = \frac{T_{2} - 294 K}{T_{2}}    

          T_{2} = 1633 K

Final temperature in degree celsius = (1633 - 273)^{o}C

                                                            = 1360^{o}C

Now, we will calculate the entropy as follows.

       \Delta S = nC_{v} ln \frac{T_{2}}{T_{1}} + nR ln \frac{P_{1}}{P_{2}}

For 1 mole,  \Delta S = C_{v} ln \frac{T_{2}}{T_{1}} + R ln \frac{P_{1}}{P_{2}}

It is known that for NH_{3} the value of C_{v} = 0.028 kJ/mol.

Therefore, putting the given values into the above formula as follows.

     \Delta S = C_{v} ln \frac{T_{2}}{T_{1}} + R ln \frac{P_{1}}{P_{2}}

                = 0.028 kJ/mol \times ln \frac{1633}{294} + 8.314 \times 10^{-3} kJ \times ln \frac{200}{1000}

                = 0.0346 kJ/mol

or,             = 34.6 J/mol             (as 1 kJ = 1000 J)

Therefore, entropy change of ammonia is 34.6 J/mol.

3 0
2 years ago
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