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Chem 2 questions 21.An ideal gas originally at 0.85 atm and 66 degree C was allo

ID: 882102 • Letter: C

Question

Chem 2 questions

21.An ideal gas originally at 0.85 atm and 66 degree C was allowed to expand until its final volume, pressure, and temperature were 94 mL, 0.60 atm, and 45 degree C, respectively. What was its initial volume? 22. What is the osmotic pressure (in atm ) of a 1.57M aqueous solution of urea [(NH2)2C0] at 27.0 degree C? 23. In the following phase diagram, what is occurring at point B? 24. For dilute aqueous solutions in which the density of the solution is roughly equal to that of the pure solvent, the molarity of the solution is equal to its molality. Show that this statement is correct for a 0.010-Maqueous urea (NH2)2C0 solution with a density of 1g/mL (hint: assume you have 10 L of the solution)

Explanation / Answer

Q21 solution

Given data

Original pressure P1 = 0 .85 atm

Original temperature T= 66 C +273 = 339K

Original volume V1 = ?

Final pressure P2 =0.60 atm

Final volume V2= 94 ml

Final temperature T2 = 45 C +273 = 318 K

Using the combined gas law formula we can calculate the original volume of the gas

P1V1/T1 = P2V2/T2

Rearranging this equation we get

V1 = P2V2*T1 / P1T2

Lets put the values in the formula

V1 = 0.60 atm * 94 ml * 339 K / 0.85 atm * 318 K

V1 = 70.7 ml

We can round it to 71 ml

So the original volume of the gas = 71 ml

Q22 solution :-

Given data

Molarity of the urea =1.57 M

Temperature = 27 C +273 = 300 K

Osmotic pressure = ?

Formula to calculate osmotic pressure is as follows

= MRT

Where , T= temperature , M= molarity

R= 0.08206 L atm per K. mol

Lets put the values in the formula

= 1.57 M * 0.08206 L atm per K mol * 300 K

= 38.7 atm

Therefore osmotic pressure of the solution = 38.7 atm.

Q23 Solution in the phase diagram at the point B supercritical liquid is forming.

Q24 solution

Given Urea solution is 0.01 M

Lets assume we have 1.0 L solution and its density is 1 g/ml

0.01 moles of urea are present in the solution therefore

0.01 mol urea * 60.06 g per mol = 0.606 g urea

therefore if we find the total mass of solution then its 1000 g + 0.60 g = 1000.6 g

1000.6 g * 1 kg / 1000 g = 1.0006 kg

Molality = moles / kg solvent =0.01 mol / 1.0 kg = 0.010 m

Therefore molarity and molality of the dilute solution is same.

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