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Ch.10 Acids and Bases
Chapter 10, Problem 34

Electrostatic potential maps of acetic acid (CH₃CO₂H) and ethyl alcohol (CH₃CH₂OH) are shown. Identify the most acidic hydrogen in each, and tell which of the two is likely to be the stronger acid. Electrostatic potential maps of acetic acid (CH₃COOH) and ethyl alcohol (CH₃CH₂OH) for acid strength comparison.

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1
Identify the acidic hydrogen in acetic acid (CH₃CO₂H) by looking for the hydrogen atom attached to the oxygen in the carboxyl group (COOH).
Identify the acidic hydrogen in ethyl alcohol (CH₃CH₂OH) by looking for the hydrogen atom attached to the oxygen in the hydroxyl group (OH).
Compare the electrostatic potential maps: areas in red indicate regions of high electron density, while blue indicates regions of low electron density.
Note that the hydrogen in the carboxyl group of acetic acid is more acidic due to the resonance stabilization of the carboxylate ion formed after deprotonation.
Determine which compound is the stronger acid by considering the stability of the conjugate base; acetic acid is likely the stronger acid due to the resonance stabilization of its conjugate base.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Acidity and Acid Strength

Acidity refers to the ability of a substance to donate protons (H⁺ ions) in a solution. The strength of an acid is determined by its dissociation constant (Ka), which measures how completely an acid ionizes in water. Stronger acids have higher Ka values and more readily release protons, making them more effective in chemical reactions.
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Electrostatic Potential Maps

Electrostatic potential maps visually represent the distribution of electron density around a molecule. Areas of high electron density are shown in blue, while low density is indicated in red. These maps help identify regions of partial positive and negative charges, which are crucial for understanding reactivity and acidity, particularly in determining the most acidic hydrogen in a molecule.
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Identifying Acidic Hydrogens

In organic acids, the most acidic hydrogen is typically attached to a functional group that can stabilize the resulting anion after deprotonation. For acetic acid (CH₃COOH), the hydrogen on the carboxylic group (-COOH) is the most acidic, while in ethyl alcohol (CH₃CH₂OH), the hydroxyl group (-OH) contains the acidic hydrogen. The stability of the anion formed after losing this hydrogen influences the overall acidity.
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