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At ordinary body temperature \(\left(37^{\circ} \mathrm{C}\right)\) the solubility of \(\mathrm{N}_{2}\) in water in contact with air at ordinary atmospheric pressure \((1.0 \mathrm{~atm})\) is \(0.015 \mathrm{~g} / \mathrm{L}\). Air is approximately \(78 \mathrm{~mol} \% \mathrm{~N}_{2}\). Calculate the number of moles of \(\mathrm{N}_{2}\) dissolved per liter of blood, which is essentially an aqueous solution. At a depth of \(100 \mathrm{ft}\) in water, the pressure is \(4.0 \mathrm{~atm}\). What is the solubility of \(\mathrm{N}_{2}\) from air in blood at this pressure? If a scuba diver suddenly surfaces from this depth, how many milliliters of \(\mathrm{N}_{2}\) gas, in the form of tiny bubbles, are released into the bloodstream from each liter of blood?

Short Answer

Expert verified
The number of moles of N₂ dissolved per liter of blood at 1 atm is \(\frac{0.015 \, \text{g}}{28 \, \text{g/mol}}\). At 4 atm, the solubility of N₂ in blood increases proportionally, resulting in a solubility of \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\) × \(\frac{4 \, \text{atm}}{1 \, \text{atm}}\). The solubility difference between these two pressures is \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\) × \(\frac{4 \, \text{atm}}{1 \, \text{atm}}\) - \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\). Converting this difference in moles to milliliters of N₂ gas, we find that when a scuba diver suddenly surfaces from 100 ft, approximately \(15.3 \, \text{mL}\) of N₂ gas is released into the bloodstream as tiny bubbles per liter of blood.

Step by step solution

01

Find the number of moles of N₂ per liter of blood at 1 atm

At ordinary body temperature and atmospheric pressure, the solubility of N₂ is given as 0.015 g/L. We need to convert the mass of N₂ into moles. To do that, we can use the molar mass of N₂, which is 28 g/mol. Number of moles = (Mass of N₂) / (Molar mass of N₂) So, Number of moles = \(\frac{0.015 \, \text{g}}{28 \, \text{g/mol}}\)
02

Calculate the number of moles of N₂ per liter of blood at 4 atm

According to Henry's law, the solubility of a gas is directly proportional to the partial pressure of the gas. Since the pressure increases from 1 atm to 4 atm, the solubility of N₂ will also increase proportionally. Solubility at 4 atm = Solubility at 1 atm × (Pressure at 4 atm / Pressure at 1 atm) So, Solubility at 4 atm = \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\) × \(\frac{4 \, \text{atm}}{1 \, \text{atm}}\)
03

Calculate the amount of N₂ released when the pressure decreases from 4 atm to 1 atm

Now we need to calculate the difference in solubility of N₂ at 4 atm and 1 atm to find the amount of N₂ released when the pressure drops. Solubility difference = Solubility at 4 atm - Solubility at 1 atm So, Solubility difference = \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\) × \(\frac{4 \, \text{atm}}{1 \, \text{atm}}\) - \(\frac{0.015 \, \text{g/L}}{28 \, \text{g/mol}}\)
04

Convert the difference in solubility (moles) into milliliters of N₂ gas

Finally, we'll convert the difference in solubility from moles to milliliters of N₂ gas. To do this, we'll use the relationship 1 mole of any gas occupies 22.4 L at standard temperature and pressure (STP). First, convert the difference in moles to millimoles: \[\text{Difference in millimoles of N₂} = \;\text{Solubility difference} \times 1000\] Now, using the relationship mentioned above, convert millimoles to milliliters of N₂ gas: \[\text{Difference in milliliters of N₂ gas} = \;\text{Difference in millimoles}\] × \(\frac{22.4 \, \text{L}}{1000 \, \text{mmol}}\) × 1000\] Once you've calculated the difference in milliliters of N₂ gas, you have the answer - the amount of N₂ released into the bloodstream as tiny bubbles per liter of blood when a scuba diver suddenly surfaces from a depth of 100 ft.

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Most popular questions from this chapter

At \(63.5^{\circ} \mathrm{C}\) the vapor pressure of \(\mathrm{H}_{2} \mathrm{O}\) is 175 torr, and that of ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) is 400 torr. A solution is made by mixing equal masses of \(\mathrm{H}_{2} \mathrm{O}\) and \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\). (a) What is the mole fraction of ethanol in the solution? (b) Assuming ideal- solution behavior, what is the vapor pressure of the solution at \(63.5^{\circ} \mathrm{C} ?\) (c) What is the mole fraction of ethanol in the vapor above the solution?

At \(35^{\circ} \mathrm{C}\) the vapor pressure of acetone, \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CO}\), is 360 torr, and that of chloroform, \(\mathrm{CHCl}_{3}\), is 300 torr. Acetone and chloroform can form weak hydrogen bonds between one another as follows: A solution composed of an equal number of moles of acetone and chloroform has a vapor pressure of 250 torr at \(35^{\circ} \mathrm{C}\). (a) What would be the vapor pressure of the solution if it exhibited ideal behavior? (b) Use the existence of hydrogen bonds between acetone and chloroform molecules to explain the deviation from ideal behavior. (c) Based on the behavior of the solution, predict whether the mixing of acetone and chloroform is an exothermic \(\left(\Delta H_{\text {soln }}<0\right)\) or endothermic \(\left(\Delta H_{\text {soln }}>0\right.\) ) process.

When \(0.55 \mathrm{~g}\) of pure benzoic acid \(\left(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH}\right)\) is dissolved in \(32.0 \mathrm{~g}\) of benzene \(\left(\mathrm{C}_{6} \mathrm{H}_{6}\right)\), the freezing point of the solution is \(0.36^{\circ} \mathrm{C}\) lower than the freezing point value of \(5.5^{\circ} \mathrm{C}\) for the pure solvent. (a) Calculate the molecular weight of benzoic acid in benzene. (b) Use the structure of the solute to account for the observed value:

List the following aqueous solutions in order of decreasing freezing point: \(0.040 \mathrm{~m}\) glycerin \(\left(\mathrm{C}_{3} \mathrm{H}_{8} \mathrm{O}_{3}\right), 0.020 \mathrm{~m}\) \(\mathrm{KBr}, 0.030 \mathrm{~m}\) phenol \(\left(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{OH}\right)\).

Show that the vapor-pressure reduction, \(\Delta P_{\text {solvent }}\), associated with the addition of a nonvolatile solute to a volatile solvent is given by the equation \(\Delta P_{\text {solvent }}=\) \(X_{\text {solute }} \times P_{\text {solvent }}^{\circ}\).

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