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Ch.16 - Acid-Base Equilibria
Chapter 16, Problem 11b

Consider the molecular models shown here, where X represents a halogen atom. (b) Does the acidity of each molecule increase or decrease as the electronegativity of the atom X increases?

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Key Concepts

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

Electronegativity

Electronegativity is a measure of an atom's ability to attract and hold onto electrons in a chemical bond. In the context of halogens, as electronegativity increases, the atom's ability to stabilize negative charge also increases, which can influence the acidity of the molecule. Higher electronegativity typically leads to stronger bonds with hydrogen, affecting the molecule's tendency to donate protons.
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Electronegativity Trends

Acidity

Acidity refers to the ability of a substance to donate protons (H⁺ ions) in a solution. The strength of an acid is often determined by the stability of the conjugate base formed after the proton is lost. In the case of halogen-containing acids, the more electronegative the halogen, the more stable the conjugate base, which generally results in increased acidity.
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Conjugate Base Stability

The stability of a conjugate base is crucial in determining the strength of an acid. A more stable conjugate base is less likely to re-accept a proton, thus favoring the dissociation of the acid. In halogen acids, as the electronegativity of the halogen increases, the conjugate base becomes more stable due to the effective delocalization of negative charge, leading to increased acidity.
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Related Practice
Textbook Question

Phenylephrine, an organic substance with molecular formula C9H13NO2, is used as a nasal decongenstant in over-thecounter medications. The molecular structure of phenylephrine is shown below using the usual shortcut organic structure. (a) Would you expect a solution of phenylephrine to be acidic, neutral, or basic?

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Textbook Question

Phenylephrine, an organic substance with molecular formula C9H13NO2, is used as a nasal decongenstant in over-thecounter medications. The molecular structure of phenylephrine is shown below using the usual shortcut organic structure. (c) Would you expect a solution of phenylephrine hydrochloride to be acidic, neutral, or basic?

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Textbook Question

Consider the molecular models shown here, where X represents a halogen atom. (a) If X is the same atom in both molecules, which molecule will be more acidic?

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Textbook Question

NH31g2 and HCl(g) react to form the ionic solid NH4Cl1s2. Which substance is the Brønsted–Lowry acid in this reaction? Which is the Brønsted–Lowry base?

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Textbook Question

Which of the following statements is false? (a) An Arrhenius base increases the concentration of OH- in water. (b) A Brønsted-Lowry base is a proton acceptor. (c) Water can act as a Brønsted–Lowry acid. (d) Water can act as a Brønsted–Lowry base. (e) Any compound that contains an –OH group acts as a Brønsted-Lowry base.

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Textbook Question

Give the conjugate base of the following Brønsted–Lowry acids: (i) HIO3, (ii) NH4+.

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