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What is the maximum amount of work that can be obtained from hydrolyzing 1 mole of ATP to ADP and phosphate at \(298 \mathrm{~K}\) ? Assume that the concentrations of all reactants are \(0.01 \mathrm{M}\) and \(\Delta G^{\circ}\) is \(-32.5 \mathrm{~kJ} / \mathrm{mol}\). If the conversion of free energy to mechanical work is \(100 \%\) efficient, how many moles of ATP would have to be hydrolyzed to lift a \(100 \mathrm{~kg}\) weight 1 meter high?

Short Answer

Expert verified
Maximum work from 1 mole ATP is 44.4 kJ; 0.022 moles ATP lifts the weight.

Step by step solution

01

Determine the reaction quotient (Q)

Using the given concentrations of reactants, calculate the reaction quotient (Q) of the hydrolysis reaction: \[ Q = \frac{{\text{{[ADP]}} \times \text{{[Pi]}}}}{{\text{{[ATP]}}}} = \frac{{0.01 \times 0.01}}{{0.01}} = 0.01 \] where [ADP], [Pi], and [ATP] are the concentrations of ADP, phosphate (Pi), and ATP respectively.
02

Calculate the actual Gibbs free energy (ΔG)

Use the equation that relates standard Gibbs energy change and the reaction quotient: \[ \Delta G = \Delta G^{\circ} + RT \ln(Q) \] Here, \( \Delta G^{\circ} = -32.5 \mathrm{~kJ/mol} \), \( R = 8.314 \times 10^{-3} \mathrm{~kJ/(mol \cdot K)} \), and \( T = 298 \mathrm{~K} \). Thus, \[ \Delta G = -32.5 + (8.314 \times 10^{-3} \times 298 \times \ln(0.01)) \approx -32.5 - 11.9 \approx -44.4 \mathrm{~kJ/mol} \]
03

Calculate the work for lifting the weight

The work done to lift a weight is given by \( W = mgh \). Given that \( m = 100 \mathrm{~kg} \), \( g = 9.8 \mathrm{~m/s^2} \), and \( h = 1 \mathrm{~m} \), the work required is: \[ W = 100 \times 9.8 \times 1 = 980 \mathrm{~J} = 0.98 \mathrm{~kJ} \]
04

Calculate number of moles of ATP required

Since the conversion of free energy to work is 100% efficient, the maximum work obtainable per mole of ATP is \(-\Delta G = 44.4 \mathrm{~kJ/mol}\). Divide the work required by the work obtainable per mole of ATP: \[ \text{{Moles of ATP}} = \frac{{0.98 \mathrm{~kJ}}}{{44.4 \mathrm{~kJ/mol}}} \approx 0.022 \text{{ moles}} \]
05

Conclusion: Calculate the maximum work and required ATP

The maximum work obtainable from hydrolyzing 1 mole of ATP is \( 44.4 \mathrm{~kJ} \). To lift a 100 kg weight 1 meter requires roughly \( 0.022 \) moles of ATP.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

ATP Hydrolysis
ATP, which stands for adenosine triphosphate, is often referred to as the energy currency of the cell. ATP hydrolysis is the process of breaking down ATP into adenosine diphosphate (ADP) and inorganic phosphate (Pi). This reaction releases energy that can be used by cells to perform various functions. At physiological conditions, ATP undergoes hydrolysis in the presence of water, resulting in the release of a significant amount of energy.
  • The reaction is typically represented as: ATP + H2O → ADP + Pi + Energy.
  • The standard change in free energy (ΔG°) for this reaction is often negative, showing that it is exergonic and releases energy.
The reaction is spontaneous under standard conditions due to the high energy stored in the phosphate bonds of ATP. By understanding ATP hydrolysis, you can see how cells power various processes, like muscle contraction and synthesis of biomolecules.
In practical settings, medical and biological research utilizes ATP hydrolysis to explore enzyme functions and cellular energy management.
Gibbs Free Energy
Gibbs free energy is a concept in thermodynamics that helps us understand and predict the feasibility of a chemical reaction. Gibbs energy combines two important thermodynamic properties: enthalpy (heat content) and entropy (degree of disorder). The equation is given by:\[ G = H - TS \]where:
  • \( G \) is the Gibbs free energy,
  • \( H \) is the enthalpy,
  • \( T \) is the temperature in Kelvin, and
  • \( S \) is the entropy.
If ΔG (change in Gibbs free energy) is negative, the reaction is spontaneous, meaning it can occur without needing external energy input. In scenarios like ATP hydrolysis, a negative ΔG indicates that the reaction will release energy that can be harnessed efficiently.
By calculating ΔG under specific conditions, you determine the actual energy available in a system, like in the given problem where hydrolyzing ATP resulted in a ΔG of -44.4 kJ/mol, highlighting available energy for work conversion.
Mechanical Work Conversion
In the context of thermodynamics and ATP hydrolysis, mechanical work conversion involves taking the energy released from chemical reactions and converting it into physical movement. In the original exercise about lifting a weight with energy from ATP, this concept is a practical application.When the energy from ATP hydrolysis is used to do mechanical work, like lifting an object against Earth's gravity, the efficiency of this conversion is crucial. In ideal conditions (100% efficient), all the free energy from ATP is converted into mechanical work. For instance, the energy to lift a 100 kg weight 1 meter high is calculated as follows:\[ W = mgh \]where:
  • \( W \) is the work done,
  • \( m \) is the mass of the object,
  • \( g \) is the acceleration due to gravity, and
  • \( h \) is the height.
By converting kJ to Joules and estimating the ATP moles needed, we can see the practical energy conversion. This showcases how ATP fuels muscular activity, providing vital insights for fields such as sports science and metabolic research.
Understanding mechanical work conversion emphasizes the importance of energy balance and efficiency in biological systems.

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Most popular questions from this chapter

The following reaction is catalyzed by the enzyme creatine kinase: A. Under standard conditions \((1 \mathrm{~atm}, 298 \mathrm{~K}, \mathrm{pH} 7.0 . \mathrm{pMg} 3.0\) and an ionic strength of \(0.25 \mathrm{M}\) ) with the concentrations of all reactants equal to \(10 \mathrm{mM}\), the free energy change, \(\Delta G\), for this reaction is \(13.3 \mathrm{~kJ} / \mathrm{mol}\). What is the standard free energy change, \(\Delta G^{\circ}\), for this reaction? B. What is the equilibrium constant for this reaction? C. The standard enthalpies of formation for the reactants are as follows: \(\begin{array}{ll}\text { Creatine } & -540 \mathrm{~kJ} / \mathrm{mol} \\\ \text { Creatine phosphate } & -1510 \mathrm{~kJ} / \mathrm{mol} \\ \text { ATP } & -2982 \mathrm{~kJ} / \mathrm{mol} \\ \text { ADP } & -2000 \mathrm{~kJ} / \mathrm{mol}\end{array}\) What is the standard enthalpy change, \(\Delta H^{\circ}\), for this reaction? D. What is the standard entropy change, \(\Delta S^{\circ}\), for this reaction?

The alcohol dehydrogenase reaction, which removes ethanol from your blood, proceeds according to the following reaction: \(\mathrm{NAD}^{+}+\)Ethanol \(\rightleftarrows \mathrm{NADH}+\) Acetaldehyde Under standard conditions ( \(298 \mathrm{~K}, 1 \mathrm{~atm}, \mathrm{pH} 7.0, \mathrm{pMg} 3\), and an ionic strength of \(0.25 \mathrm{M}\) ), the standard enthalpies and free energies of formation of the reactants are as follows: \begin{tabular}{lrr} & \(H^{\circ}(\mathrm{kJ} / \mathrm{mol})\) & \(G^{\circ}(\mathrm{kJ} / \mathrm{mol})\) \\ \hline NAD \(^{+}\) & \(-10.3\) & \(1059.1\) \\ NADH & \(-41.4\) & \(1120.1\) \\ Ethanol & \(-290.8\) & \(63.0\) \\ Acetaldehyde & \(-213.6\) & \(24.1\) \\ \hline \end{tabular} A. Calculate \(\Delta G^{\circ}, \Delta H^{\circ}\), and \(\Delta S^{\circ}\) for the alcohol dehydrogenase reaction under standard conditions. B. Under standard conditions, what is the equilibrium constant for this reaction? Will the equilibrium constant increase or decrease as the temperature is increased?

The equilibrium constant under standard conditions \((1 \mathrm{~atm}, 298 \mathrm{~K}, \mathrm{pH} 7,0)\) for the reaction catalyzed by fumarase, Fumarate \(+\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \mathrm{L}\)-malate is \(4.00\). At \(310 \mathrm{~K}\), the equilibrium constant is \(8.00\). A. What is the standard free energy change, \(\Delta G^{\circ}\), for this reaction? B. What is the standard enthalpy change, \(\Delta H^{\circ}\), for this reaction? Assume the standard enthalpy change is independent of temperature. C. What is the standard entropy change, \(\Delta 5^{\circ}\), at \(298 \mathrm{~K}\) for this reaction? D. If the concentration of both reactants is equal to \(0.01 \mathrm{M}\), what is the free energy change at \(298 \mathrm{~K}\) ? As the reaction proceeds to equilibrium, will more fumarate or L-malate form? E. What is the free energy change for this reaction when equilibrium is reached?

A. It has been proposed that the reason ice skating works so well is that the pressure from the blades of the skates melts the ice. Consider this proposal from the viewpoint of phase equilibria, The phase change in question is $$ \mathrm{H}_{2} \mathrm{O}(\mathrm{s}) \rightleftharpoons \mathrm{H}_{2} \mathrm{O}(/) $$ Assume that \(\Delta H\) for this process is independent of temperature and pressure and is cqual to 80 cal/g. The change in volume, \(\Delta V\), is about \(-9.1 \times\) \(10^{-5} \mathrm{~L} / \mathrm{g}\). The pressure exerted is the force per unit area. For a 180 pound person and an area for the skate blades of about 6 square inches, the pressure is \(30 \mathrm{lb} / \mathrm{sq}\). in. or about 2 atmospheres. With this information, calculate the decrease in the melting temperature of ice caused by the skate blades. (Note that 1 cal \(=0.04129\) L.atm.) Is this a good explanation for why ice skating works? B. A more efficient way of melting ice is to add an inert compound such as urea. (We will avoid salt to save our cars.) The extent to which the freexing point is lowered can be calculated by noting that the molar free energy of water must be the same in the solid ice and the urea solution. The molar free energy of water in the urea solution can be approximated as \(G_{\text {liquid }}^{\circ}+R T \ln X_{\text {water }}\) where \(X_{\text {water }}\) is the mole fraction of water in the solution. The molar free energy of the solid can be written as \(G_{\text {solid }}^{\circ}\). Derive an expression for the change in the melting temperature of ice by equating the free energies in the two phases, differentiating the resulting equation with respect to temperature, integrating from a mole fraction of 1 (pure solvent) to the mole fraction of the solution, and noting that \(\ln X_{\text {wamer }}=\ln \left(1-X_{\text {urea }}\right)\) \(=-X_{\text {urea }}\) (This relationship is the series expansion of the logarithm for small values of \(X_{\text {unea }}\). Since the concentration of water is about \(55 \mathrm{M}\), this is a good approximation.) With the relationship derived, estimate the de- crease in the melting temperature of ice for an \(1 \mathrm{M}\) urea solution. The heat of fusion of water is \(1440 \mathrm{cal} / \mathrm{mol}\).

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