Vapor pressure of ethanoic acid vs. ethanol

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SUMMARY

The discussion centers on the vapor pressure comparison between ethanoic acid and ethanol, concluding that ethanoic acid has a lower vapor pressure due to its ability to form strong hydrogen bonds and dimers. Ethanoic acid's polar C=O bond enhances dipole-dipole interactions, which further stabilizes the dimers. Participants agree that the correct answer to the vapor pressure question is option B, emphasizing the significance of molecular interactions in determining vapor pressure.

PREREQUISITES
  • Understanding of hydrogen bonding and molecular interactions
  • Familiarity with the structures of ethanoic acid and ethanol
  • Knowledge of vapor pressure concepts
  • Basic chemistry principles related to polarity and intermolecular forces
NEXT STEPS
  • Research the effects of hydrogen bonding on vapor pressure in organic compounds
  • Study the molecular structure of ethanoic acid and its implications for intermolecular forces
  • Learn about dimer formation in organic acids and its impact on physical properties
  • Explore the role of polarity in determining the physical properties of molecules
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Chemistry students, educators, and professionals interested in organic chemistry, particularly those studying molecular interactions and their effects on physical properties like vapor pressure.

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Homework Statement
Ethanoic acid (CH3COOH) has a much lower vapor pressure than ethanol (CH3CH2OH). What is the most reasonable explanation?

A) The polarizability of 2 oxygen atoms increases London forces of attraction in ethanoic acid compared with ethanol.
B) Hydrogen bonding in ethanoic acid is the strongest attractive force and is mainly responsible for the observed data.
C) Ethanol has a -OH group and can hydrogen bond; therefore the London forces must cause the effect.
D) Both ethanol and ethanoic acid have an -OH, so the difference is the dipole of the 2nd oxygen that increases the attractive forces.
Relevant Equations
intermolecular forces
I think the answer is D because both molecules can hydrogen bond with their OH groups, but the C=O bond in ethanoic acid is polar and contributes to dipole-dipole interactions.

The solution says B is the correct answer, because ethanoic acid molecules strongly hydrogen bond so that most molecules are part of dimers. I don't really understand this, and why I'm wrong. Could anyone help me? Thanks.
 
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Yes, B is correct. Arrange two molecules so that the OH group of one is close to the C=O group of the other, yin/yang fashion.
 

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