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inna [77]
2 years ago
13

What is the entropy change of the system when 17.5 g of liquid benzene (c6h6) evaporates at the normal boiling point? the normal

boiling point of benzene is 80.1°c and δhvap is 30.7 kj/mol?
Chemistry
2 answers:
ivanzaharov [21]2 years ago
8 0

Answer : The entropy change of the system is, 19.5 J/K

Solution :

Formula used :

\Delta S=\frac{n\times \Delta H_{vap}}{T_b}

or,

\Delta S=\frac{\frac{w}{M}\times \Delta H_{vap}}{T_b}

where,

\Delta S = entropy change of the system = ?

\Delta H = enthalpy of vaporization = 30.7 kJ/mole

n = number of moles of benzene

w = mass of benzene = 17.5 g

M = molar mass of benzene = 78 g/mole

T_b = normal boiling point of benzene = 80.1^oC=273+80.1=353.1K

Now put all the given values in the above formula, we get the entropy change of the system.

\Delta S=\frac{\frac{17.5g}{78g/mole}\times (30.7KJ/mole)}{353.1K}=0.0195kJ/K=0.0195\times 1000=19.5J/K

Therefore, the entropy change of the system is, 19.5 J/K

Vika [28.1K]2 years ago
7 0
<span>1 mole of benzene (78g) requires 30.8 kJ/ of heat, so 11.5g will need ..... (it's a proportion calculation.) Temperature does not change at BPt and is not relevant if the temp of the liquid is already at the BPt ne definition of entropy is qrev/T, where qrev is the heat added in reversible operation (for complicated reasons pertaining to heat as a path function) and T is the temperature at which this is done. Phase changes are particularly good examples for calculations of changes in entropy, since temperature will not change will the bonds of a state are being broken. The calculations required boils down to: 1) finding the moles of benzene given from molar mass. 2) multiplying that moles by the heat of vaporization. 3)diving the heat energy required by the temperature of boiling point.</span>
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5.00 g of hydrogen gas and 50.0g of oxygen gas are introduced into an otherwise empty 9.00L steel cylinder, and the hydrogen is
GenaCL600 [577]
1) Balanced chemical reaction:

2H2 + O2 -> 2H20

Sotoichiometry: 2 moles H2: 1 mol O2 : 2 moles H2O

2) Reactant quantities converted to moles

H2: 5.00 g / 2 g/mol = 2.5 mol

O2: 50.0 g / 32 g/mol = 1.5625 mol

Limitant reactant: H2 (because as per the stoichiometry it will be consumed with 1.25 mol of O2).

3) Products

H2 totally consumed -> 0 mol at the end

O2 = 1.25 mol consumed -> 1.5625 mol - 1.25 mol = 0.3125 mol at the end

H2O: 2.5 mol H2 produces 2.5 mol H2O -> 2.5 mol at the end.

Total number of moles: 0.3125mol + 2.5 mol = 2.8125 mol

4) Pressure

Use pV = nRT
n = 2.8125
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3 0
2 years ago
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When of benzamide are dissolved in of a certain mystery liquid , the freezing point of the solution is less than the freezing po
SOVA2 [1]

The given question is incomplete. The complete question is as follows.

When 70.4 g of benzamide (C_{7}H_{7}NO) are dissolved in 850 g of a certain mystery liquid X, the freezing point of the solution is 2.7^{o}C lower than the freezing point of pure X. On the other hand, when 70.4 g of ammonium chloride (NH_{4}Cl) are dissolved in the same mass of X, the freezing point of the solution is 9.9^{o}C lower than the freezing point of pure X.

Calculate the Van't Hoff factor for ammonium chloride in X.

Explanation:

First, we will calculate the moles of benzamide as follows.

    Moles of benzamide = \frac{mass}{\text{Molar mass of benzamide}}

                    = \frac{70.4 g}{121.14 g/mol}

                    = 0.58 mol

Now, we will calculate the molality as follows.

     Molality = \frac{\text{moles of solute (benzamide)}}{\text{solvent mass in kg}}

                   = \frac{0.58 mol}{0.85 kg}

                   = 0.6837

It is known that relation between change in temperature, Van't Hoff factor and molality is as follows.

      dT = i \times K_{f} \times m,

where,      dT = change in freezing point = 2.7^{o}C

                  i = van't Hoff factor = 1 for non dissociable solutes

      K_{f} = freezing point constant of solvent

                m = 0.6837

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

             dT = i \times K_{f} \times m,

            2.7^{o}C = 1 \times K_{f} \times 0.6837 m

            K_{f} = 3.949 C/m

Now, we use this K_{f} value for calculating i for NH_{4}Cl

So, moles of ammonium chloride are calculated as follows.

 Moles of NH_{4}Cl = \frac{70.4 g}{53.491 g/mol}

                            = 1.316 mol

Hence, calculate the molality as follows.

    Molality = \frac{1.316 mol}{0.85 kg}

                  = 1.5484

It is given that value of change in temperature (dT) = 9.9^{o}C. Thus, calculate the value of Van't Hoff factor as follows.

              dT = i \times K_{f} \times m

   9.9^{o}C = i \times 3.949 C/m \times 1.5484 m

                     i = 1.62

Thus, we can conclude that the value of van't Hoff factor for ammonium chloride is 1.62.

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2 years ago
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Bogdan [553]
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(4) The overall energy conversion in power plants is chemical to electrical while in dams it is potential to electrical.

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8 0
2 years ago
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Liquid nitrogen has a density of 0.807 g/ml at –195.8 °c. if 1.00 l of n2(l) is allowed to warm to 25°c at a pressure of 1.00 at
Flauer [41]
Step 1: Change density from g/mL to g/L;

                                  0.807 g/mL  =  807 g/L

Step 2: Find Moles of N₂;
As,
             Density  =  Mass / Volume
Or,
             Mass  =  Density × Volume

Putting Values,

            Mass  =  807 g/L × 1 L

            Mass  =  807 g
Also,
            Moles  =  Mass / M.mass

Putting values,

            Moles  =  807 g / 28 g.mol⁻¹

            Moles  =  28.82 moles

Step 3: Apply Ideal Gas Equation to Find Volume of gas occupied,

As,
                        P V  =  n R T

                            V  =  n R T / P
Putting Values, remember! don't forget to change temperatue into Kelvin (25 °C + 273 = 298 K)

                 V  =  (28.82 mol × 0.08206 atm.L.mol⁻¹.K⁻¹ × 298 K) ÷ 1 atm

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8 0
2 years ago
The ΔG°f of atomic oxygen is 230.1 kJ/mol. Find ΔG° for the following dissociation reactionO2 (g) &lt;--&gt; 2O (g)then calculat
marusya05 [52]

Answer:

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Explanation:

Let's consider the following reaction:

O₂(g) ⇄ 2O(g)

The standard Gibbs free energy for the reaction (ΔG°) can be calculated using the following expression:

ΔG° = Σnp. ΔG°f(p) - Σnp. ΔG°f(p)

where,

ni are the moles of products and reactants

ΔG°f(p) are the standard Gibbs free energy of formation of products and reactants

In this case,

ΔG° = 2 × ΔG°f(O) - 1 × ΔG°f(O₂)

ΔG° = 2 × 230.1 kJ/mol - 1 × 0 kJ/mol

ΔG° = 460.2 kJ/mol

With this information, we can calculate the equilibrium constant (Kc) using the following expression:

Kc=e^{-\Delta G \°/R.T } = e^{-460.2 kJ/mol/(8.314 \times 10^{-3}kJ/mol.K)  \times 298K }=2.145 \times 10^{-81}

3 0
2 years ago
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