A muscle can be thought of as a fuel cell, producing work from the metabolism of glucose:

C6H12O6+6O26CO2+6H2O

(a) Use the data at the back of this book to determine the values of ΔHand ΔGfor this reaction, for one mole of glucose. Assume that the reaction takes place at room temperature and atmospheric pressure.

(b) What is maximum amount of work that a muscle can perform , for each mole of glucose consumed, assuming ideal operation?

(c) Still assuming ideal operation, how much heat is absorbed or expelled by the chemicals during the metabolism of a mole of glucose?

(d) Use the concept of entropy to explain why the heat flows in the direction it does?

(e) How would your answers to parts (a) and (b) change, if the operation of the muscle is not ideal?

Short Answer

Expert verified

(a) The value of ΔHis -2803.04kJand the value of ΔGis -2878.94kJ.

(b) The maximum amount of workdone is 2878.94 KJ.

(c) The amount of heat absorbed is 75.9 KJ.

(d) Here, the heat is positive and entropy is positive. So, the heat flows into the system.

(e) Here less amount of energy will leave the system, but Gibbs free energy and enthalpy will be same.

Step by step solution

01

Explanation

The chemical reaction for the fuel cell of the muscle is

C6H12O6+6O26CO2+6H2O

Formula used:

Write the expression for the enthalpy change for the reaction.

ΔH=6HCo2+6HH2O-HC6H12O6-6HO2(1)

Here, HCO2is the enthalpy for CO2,HH2Ois the enthalpy of H2O,HC4H2O4is the enthalpy for C6H12O6and Ho2is the enthalpy of O2.

Write the expression for the Gibbs energy change for the reaction.

ΔG=6GCO2+6GH2O-GCbH12O4-6GO2(2)
02

Calculation

Calculation:

Refer table at the back of the book.

Substitute-285.83kJfor HCO4,-393.51kJfor HH2O,0for HCnH2O6and -1273kJfor Ho2in expression (1).

ΔH=-6(285.83kJ+393.51kJ)-6(0)+1273kJ=-2803.04kJ

Substitute-237.13kJfor GCO2,-394.36kJfor GH2O,0for GC6H2O3and -910kJfor GO2in expression (2).

ΔG=-6(237.13kJ+394.36kJ)-6(0)+910kJ=-2878.94kJ

Thus, the value of ΔH is -2803.04kJ and the value of ΔG is -2878.94kJ.

03

Step 3. (b) GIven information

The chemical reaction for the fuel cell of the muscle is

C6H12O6+6O2→6CO2+6H2O.

Workdone for ideal operation,

W=GwhereW=workdoneG=Gibbsenergy

04

Step 4. Calculation

As, G=2878.94KJ.

So,W=2878.94KJ

05

Step 5. Conclusion

The maximum amount of workdone is 2878.94 KJ.

06

Step 5. Given information

The chemical reaction for the fuel cell of the muscle is

C6H12O6+6O2→6CO2+6H2O.

The enthalpy is less than the amount of the work extracted.

The expression for the heat absorbed.

Q=W-∆H

where

Q=heatabsorbed.

07

Step 7. Calculation

Here

W=2878.94KJH=2803.04KJ

So,Q=2878.94KJ-2803.04KJ=75.9KJ

08

Step 8. Conclusion

The amount of heat absorbed is 75.9 KJ.

09

Step 9. Given information

The chemical reaction for the furl cell of the muscle is

C6H12O6+6O2→6CO2+6H2O.

The expression for the entropy change for the reaction.

S=6SCO2+6SH2O-SC6H12O6-6SO2·······(3)whereSCO2=EntropyforCO2SH2O=EntropyofH2OSC6H12O6=EntropyofC6H12O6SO2=EntropyofO2

Entropy in terms of heat absorbed

S=QT········(4)whereQ=heatabsorbedT=absolutetemperature

10

Step 10. Calculation

From the table

SCO2=69.91J·K-1SH2O=213.74J·K-1SC6H12O6=205.14J·K-1SO2=212J·K-1

So,

S=669.91+213.74=6205.14-212J·K-1=259.06J·K-1

Hence,

Q=259.06J·K-1298K=77.2KJ

11

Step 11. Conclusion

Thus, the heat is positive and entropy is also positive. So, the heat flows into the system.

12

Step 12. Given information

The chemical reaction for the fuel cell of the muscle is

C6H12O6+6O2→6CO2+6H2O.

In the ideal reaction, the work equals the change in the Gibbs energy. But when the reaction is not ideal the amount of work is less than the Gibbs energy. Here, as the change of entropy is same, therefore less heat flow enters the system and less energy leaves the system. But, the Gibbs free energy and enthalpy are same whether or not the operation is ideal or not.

13

Step 13. Conclusion

Thus, less amount of energy will leave the system, but Gibbs free energy and enthalpy will be same.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Ordinarily, the partial pressure of water vapour in the air is less than the equilibrium vapour pressure at the ambient temperature; this is why a cup of water will spontaneously evaporate. The ratio of the partial pressure of water vapour to the equilibrium vapour pressure is called the relative humidity. When the relative humidity is 100%, so that water vapour in the atmosphere would be in diffusive equilibrium with a cup of liquid water, we say that the air is saturated. The dew point is the temperature at which the relative humidity would be 100%, for a given partial pressure of water vapour.

(a) Use the vapour pressure equation (Problem 5.35) and the data in Figure 5.11 to plot a graph of the vapour pressure of water from 0°C to 40°C. Notice that the vapour pressure approximately doubles for every 10° increase in temperature.

(b) Suppose that the temperature on a certain summer day is 30° C. What is the dew point if the relative humidity is 90%? What if the relative humidity is 40%?

Consider a completely miscible two-component system whose overall composition is x, at a temperature where liquid and gas phases coexist. The composition of the gas phase at this temperature is xaand the composition of the liquid phase is xb. Prove the lever rule, which says that the proportion of liquid to gas is x-xa/xb-x. Interpret this rule graphically on a phase diagram.

When plotting graphs and performing numerical calculations, it is convenient to work in terms of reduced variables, Rewrite the van der Waals equation in terms of these variables, and notice that the constants a and b disappear.

The methods of this section can also be applied to reactions in which one set of solids converts to another. A geologically important example is the transformation of albite into jadeite + quartz:

NaAlSi3O8NaAlSi2O6+SiO2

Use the data at the back of this book to determine the temperatures and pressures under which a combination of jadeite and quartz is more stable than albite. Sketch the phase diagram of this system. For simplicity, neglect the temperature and pressure dependence of both S and V.

In Problems 3.30 and 3.31 you calculated the entropies of diamond and graphite at 500 K. Use these values to predict the slope of the graphite- diamond phase boundary at 500 K, and compare to Figure 5.17. Why is the slope almost constant at still higher temperatures? Why is the slope zero at T = 0?

See all solutions

Recommended explanations on Physics Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free