Phosgene, COCl 2 , can be formed by the reaction of chloroform, CHCl 3 ( l ), with oxygen: 2 CHCl 3 ( l ) + O 2 ( g ) → 2 COCl 2 ( g ) + 2 HCl ( g ) Δ H ° = − 353.2 kJ ; Δ G ° = − 452.4 kJ at 25°C (a) Calculate Δ S ° for the reaction. Is the sign reasonable? (b) Calculate S ° for phosgene. (c) Calculate Δ H f ° for phosgene.
Phosgene, COCl 2 , can be formed by the reaction of chloroform, CHCl 3 ( l ), with oxygen: 2 CHCl 3 ( l ) + O 2 ( g ) → 2 COCl 2 ( g ) + 2 HCl ( g ) Δ H ° = − 353.2 kJ ; Δ G ° = − 452.4 kJ at 25°C (a) Calculate Δ S ° for the reaction. Is the sign reasonable? (b) Calculate S ° for phosgene. (c) Calculate Δ H f ° for phosgene.
Solution Summary: The author explains that the entropy of the given reaction at 25°C is -0.0037 kJ/K mol. The standard free energy of formation refers to the energy change which occurs when a compound
CHEM2323
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PS CH03
Draw and name all monobromo derivatives of pentane, C5H11Br.
Problem 3-33
Name:
Draw structures for the following:
(a) 2-Methylheptane
(d) 2,4,4-Trimethylheptane
Problem 3-35
(b) 4-Ethyl-2,2-dimethylhexane
(e) 3,3-Diethyl-2,5-dimethylnonane
(c) 4-Ethyl-3,4-dimethyloctane
2
(f) 4-Isopropyl-3-methylheptane
KNIE>
Problem 3-42
Consider 2-methylbutane (isopentane). Sighting along the C2-C3 bond:
(a) Draw a Newman projection of the most stable
conformation.
(b) Draw a Newman projection of the least stable
conformation.
Problem 3-44
Construct a qualitative potential-energy diagram for rotation about the C-C bond of 1,2-dibromoethane.
Which conformation would you expect to be most stable? Label the anti and gauche conformations of 1,2-
dibromoethane.
Problem 3-45
Which conformation of 1,2-dibromoethane (Problem 3-44) would you expect to have the largest dipole
moment? The observed dipole moment of 1,2-dibromoethane is µ = 1.0 D. What does this tell you about the
actual conformation of the molecule?
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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