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.
Draw a stepwise mechanism for the following reaction.
OH
Help with annotating the labeled peaks in the 'H NMR (solvent CDCls) spectra and 'H NMR (solvent Acetone-D6) spectra Also help with Calculating the keto-enol tautomerization Ka constant for the product in both solvents.Two solvents and two different Ka
Draw a Haworth projection of a common cyclic form of this monosaccharide
CH₂OH
HO
H
HO
H
H
OH
CH₂OH
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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