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Oxana [17]
2 years ago
5

High-purity benzoic acid (C6H5COOH; ΔHrxn for combustion = −3227 kJ/mol) is used as a standard for calibrating bomb calorimeters

. A 1.221-g sample burns in a calorimeter (heat capacity = 1365 J/°C) that contains exactly 1.430 kg of water. What temperature change is observed?
Chemistry
1 answer:
melamori03 [73]2 years ago
3 0

Answer : The temperature change observed is 4.35^oC

Explanation :

First we have to calculate the heat released by the combustion of benzoic acid.

q=n\times \Delta H

where,

q = heat released by combustion of benzoic acid = ?

n = moles of benzoic acid = \frac{\text{Mass of benzoic acid}}{\text{Molar mass of benzoic acid}}=\frac{1.221g}{122.122g/mole}=0.0099mole

\Delta H = enthalpy of combustion = 3227 kJ/mole

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

q=(0.0099mole)\times (3227kJ/mole)=31.9473kJ=31947.3J

Now we have to calculate the heat absorbed.

Heat released by combustion = Heat absorbed by the calorimeter + Heat absorbed by the water

q=[q_1+q_2]

q=[c_1\times \Delta T+m_2\times c_2\times \Delta T]

where,

q = heat released by the combustion = 31947.3 J

q_1 = heat absorbed by the calorimeter

q_2 = heat absorbed by the water

c_1 = specific heat of calorimeter = 1365J/^oC

c_2 = specific heat of water = 4.18J/g^oC

m_2 = mass of water = 1.430 kg  = 1430 g

\Delta T = change in temperature = ?

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

31947.3J=[(1365J/^oC\times \Delta T)+(1430g\times 4.18J/g^oC\times \Delta T)]

\Delta T=4.35^oC

Therefore, the temperature change observed is 4.35^oC

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Answer:

a) ΔHºrxn = 116.3 kJ, ΔGºrxn = 82.8 kJ,  ΔSºrxn =  0.113 kJ/K

b) At 753.55 ºC or higher

c )ΔG =  1.8 x 10⁴ J

    K = 8.2 x 10⁻²

Explanation:

a)                                 C6H5−CH2CH3  ⇒  C6H5−CH=CH2  + H₂

ΔHf kJ/mol                    -12.5                           103.8                      0

ΔGºf kJ/K                        119.7                         202.5                      0

Sº J/mol                          255                          238                      130.6*

Note: This value was not given in our question, but is necessary and can be found in standard handbooks.

Using Hess law to calculate  ΔHºrxn we have

ΔHºrxn  = ΔHfº C6H5−CH=CH2 +  ΔHfº H₂ - ΔHºfC6H5−CH2CH3

ΔHºrxn =     103.8 kJ + 0 kJ  - (-12.5 kJ)

ΔHºrxn = 116.3 kJ

Similarly,

ΔGrxn = ΔGºf C6H5−CH=CH2 +  ΔGºfH₂ - ΔGºfC6H5CH2CH3

ΔGºrxn=   202.5 kJ + 0 kJ - 119.7 kJ  = 82.8 kJ

ΔSºrxn = 238 J/mol + 130.6 J/mol -255 J/K = 113.6 J/K = 0.113 kJ/K

b) The temperature at which the reaction is spontaneous or feasible occurs when ΔG becomes negative and using

ΔGrxn =  ΔHrxn -TΔS

we see that will happen when the term  TΔS  becomes greater than ΔHrxn since ΔS  is positive  , and so to sollve for T we will make ΔGrxn equal to zero and solve for T. Notice here we will make the assumption that  ΔºHrxn and ΔSºrxn remain constant at the higher temperature  and will equal the values previously calculated for them. Although this assumption is not entirely correct, it can be used.

0 = 116 kJ -T (0.113 kJ/K)

T = 1026.5 K  =  (1026.55 - 273 ) ºC = 753.55 ºC

c) Again we will use

                       ΔGrxn =  ΔHrxn -TΔS

to calculate ΔGrxn   with the assumption that ΔHº and ΔSºremain constant.

ΔG =  116.3 kJ - (600+273 K) x 0.113 kJ/K =  116.3 kJ - 873 K x 0.113 kJ/K

ΔG =  116.3 kJ - 98.6 kJ =  17.65 kJ = 1.8 x 10⁴ J ( Note the kJ are converted to J to necessary for the next part of the problem )

Now for solving for K, the equation to use is

ΔG = -RTlnK and solve for K

- ΔG / RT = lnK  ∴ K = exp (- ΔG / RT)

K = exp ( - 1.8 x 10⁴ J /( 8.314 J/K  x 873 K)) = 8.2 x 10⁻²

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<h3 />
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Answer:

M=0.638M

Explanation:

Hello!

In this case, since the molarity of a solution is calculated by diving the moles of solute by the volume of solution in liters, we first compute the moles of barium hydroxide in 35.5 g as shown below:

n=35.5g Ba(OH)_2*\frac{1molBa(OH)_2}{171.34gBa(OH)_2}\\\\n=0.207mol

Then, the liters of solution:

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Finally, the molarity turns out:

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