The value of q , w , Δ E , Δ S , Δ H and Δ G for the expansion of 1.00 mole of an ideal gas at 25 0 C isothermally and irreversibly from 2.45 × 10 − 2 atm to 2 .45 × 10 − 3 atm should be calculated in one step. Concept Introduction : Work done can be calculated as follows: w = − P . Δ V Δ V = V f − V i = n R T ( 1 P f − 1 P i ) The internal energy is sum of heat and work. Δ E = q + w The change in entropy is calculated as follows: Δ S = n R ln ( P 1 P 2 ) Also, change in Gibbs free energy is related to change in enthalpy and entropy as follows: Δ G = Δ H − T . Δ S w − work done P − pressure V − volume n − number of moles R − universal gas constant T − temperature ΔE − energy change q − heat ΔS − entropy change ΔG − Gibbs free energy change ΔH − enthalpy change
The value of q , w , Δ E , Δ S , Δ H and Δ G for the expansion of 1.00 mole of an ideal gas at 25 0 C isothermally and irreversibly from 2.45 × 10 − 2 atm to 2 .45 × 10 − 3 atm should be calculated in one step. Concept Introduction : Work done can be calculated as follows: w = − P . Δ V Δ V = V f − V i = n R T ( 1 P f − 1 P i ) The internal energy is sum of heat and work. Δ E = q + w The change in entropy is calculated as follows: Δ S = n R ln ( P 1 P 2 ) Also, change in Gibbs free energy is related to change in enthalpy and entropy as follows: Δ G = Δ H − T . Δ S w − work done P − pressure V − volume n − number of moles R − universal gas constant T − temperature ΔE − energy change q − heat ΔS − entropy change ΔG − Gibbs free energy change ΔH − enthalpy change
The value of q,w,ΔE,ΔS,ΔH and ΔG for the expansion of 1.00 mole of an ideal gas at 25 0C isothermally and irreversibly from 2.45×10−2 atm to 2.45 ×10−3 atm should be calculated in one step.
Concept Introduction:
Work done can be calculated as follows:
w=−P.ΔV
ΔV=Vf−Vi=nRT(1Pf−1Pi)
The internal energy is sum of heat and work.
ΔE=q+w
The change in entropy is calculated as follows:
ΔS=nRln(P1P2)
Also, change in Gibbs free energy is related to change in enthalpy and entropy as follows:
ΔG=ΔH−T.ΔS
w − work done
P − pressure
V − volume
n − number of moles
R − universal gas constant
T − temperature
ΔE − energy change
q − heat
ΔS − entropy change
ΔG − Gibbs free energy change
ΔH − enthalpy change
(a)
Expert Solution
Answer to Problem 148CP
ΔE=0ΔH=0
w=−2229 J
q=2229 J
ΔS = 19.1 J/K
ΔG = −5690 J
Explanation of Solution
ΔE=0 and ΔH=0 since ΔT = 0
ΔV=1.00 mol ×0.08206 L.atm/mol.K × 298 K (12.45×10−3 atm−12.45×10−2 atm) = 8983 L
The value of q,w,ΔE,ΔS,ΔH and ΔG for the expansion of 1.00 mole of an ideal gas at 25 0C isothermally and reversibly from 2.45×10−2 atm to 2.45 ×10−3 atm should be calculated in one step.
Concept Introduction:
The change in entropy is calculated as follows:
ΔS=qrevT
Here,
ΔS − entropy change
qrev − heat absorbed or release during reversible process
T − temperature
(b)
Expert Solution
Answer to Problem 148CP
ΔE=0ΔH=0
ΔS = 19.1 J/K
ΔG = −5690 J
qrev=5690 J
wrev=−5690 J
Explanation of Solution
ΔE=0ΔH=0
ΔS = 19.1 J/K
ΔG = −5690 J same as in part a, because these are state functions.
ΔS=qrevTqrev=T.ΔS=298 K × 19.1 J/Kqrev=5690 J
ΔE=0=q+wwrev=−qrev=−5690 J
(c)
Interpretation Introduction
Interpretation:
The value of q,w,ΔE,ΔS,ΔH and ΔG for the compression of 1.00 mole of an ideal gas at 25 0C isothermally and irreversibly from 2.45 ×10−3 atm to 2.45×10−2 atm should be calculated in one step.
Concept Introduction:
Work done can be calculated as follows:
w=−P.ΔV
ΔV=Vf−Vi=nRT(1Pf−1Pi)
The internal energy is sum of heat and work.
ΔE=q+w
The change in entropy is calculated as follows:
ΔS=nRln(P1P2)
Also, change in Gibbs free energy is related to change in enthalpy and entropy as follows:
ΔG=ΔH−T.ΔS
w − work done
P − pressure
V − volume
n − number of moles
R − universal gas constant
T − temperature
ΔE − energy change
q − heat
ΔS − entropy change
ΔG − Gibbs free energy change
ΔH − enthalpy change
(c)
Expert Solution
Answer to Problem 148CP
ΔE=0ΔH=0
ΔS = −19.1 J/K
ΔG = 5690 J
w=22300 J
q=−22300 J
Explanation of Solution
ΔE=0ΔH=0
ΔS = −19.1 J/K
ΔG = 5690 J
The signs are opposite as this is the reverse process described in part a.
Please help me calculate the undiluted samples ppm concentration.
My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve.
Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4
Provide an IUPAC name for each of the compounds shown.
(Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to
commas, dashes, etc.)
H₁₂C
C(CH3)3
C=C
H3C
CH3
CH3CH2CH
CI
CH3
Submit Answer
Retry Entire Group
2 more group attempts remaining
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Arrange the following compounds / ions in increasing nucleophilicity (least to
most nucleophilic)
CH3NH2
CH3C=C:
CH3COO
1
2
3
5
Multiple Choice 1 point
1, 2, 3
2, 1, 3
3, 1, 2
2, 3, 1
The other answers are not correct
0000
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The Laws of Thermodynamics, Entropy, and Gibbs Free Energy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=8N1BxHgsoOw;License: Standard YouTube License, CC-BY