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Compound Naphthalene, C10H8 Carbon tetrachloride, CCI4 Acetone, CH3COCH3 Benzoic acid, C,H;COOH Boiling point (°C) AHvap(kJ/mol) 218 51.5 76 31.8 56 31.8 249 68.2 a) Naphthalene has a higher boiling point than carbon tetrachloride. b) Naphthalene has a lower vaporization energy than benzoic acid.

Compound Naphthalene, C10H8 Carbon tetrachloride, CCI4 Acetone, CH3COCH3 Benzoic acid, C,H;COOH Boiling point (°C) AHvap(kJ/mol) 218 51.5 76 31.8 56 31.8 249 68.2 a) Naphthalene has a higher boiling point than carbon tetrachloride. b) Naphthalene has a lower vaporization energy than benzoic acid.

General Chemistry - Standalone book (MindTap Course List)
General Chemistry - Standalone book (MindTap Course List)
11th Edition
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Chapter11: States Of Matter; Liquids And Solids
Section: Chapter Questions
Problem 11.49QP: Chloroform, CHCl3, a volatile liquid, was once used as an anesthetic but has been replaced by safer...
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The Table below shows the boiling points and the energy required to evaporate various substances, use what we learned in chapter 3.7 regarding to intermolecular force to explain:

 

Compound Naphthalene, C10H8 Carbon tetrachloride, CCI4 Acetone, CH;COCH3 Benzoic acid, C,H5COOH Boiling point (°C) AHvap (kJ/mol) 218 51.5 76 31.8 56 31.8 249 68.2 a) Naphthalene has a higher boiling point than carbon tetrachloride. b) Naphthalene has a lower vaporization energy than benzoic acid.
Transcribed Image Text:Compound Naphthalene, C10H8 Carbon tetrachloride, CCI4 Acetone, CH;COCH3 Benzoic acid, C,H5COOH Boiling point (°C) AHvap (kJ/mol) 218 51.5 76 31.8 56 31.8 249 68.2 a) Naphthalene has a higher boiling point than carbon tetrachloride. b) Naphthalene has a lower vaporization energy than benzoic acid.
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