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Typology: Exercises
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Chapter 14 PRE-CLASS ASSIGNMENT 14. In the first half of this Chapter (14.1-14.3), we discussed how to quantitatively describe aqueous solutions of acids and bases via calculations of pH, pOH, Ka, and Kb. We also distinguished between strong and weak acids/bases, and described how strong acids/bases dissociate fully in solution whereas weak acids/bases dissociate incompletely. What’s been missing from our discussion, thus far, is a molecular-level understanding of acids and bases. Why are some acids strong while others are weak? Why does acetic acid (CH 3 COOH) react to form CH 3 COO–^ and not CH 2 COOH–? When H 2 SO 4 reacts does it lose one or both protons? Let’s find out! Watch https://youtu.be/ytULYN-D3l4. Define each of the following terms: Binary acid: An acid composed of hydrogen and one other nonmetal element. Oxoacid: An acid that contains hydrogen, oxygen, and another element (the central atom). Polyprotic Acid: An acid that can donate more than one proton per molecule. Explain how each of the following factors influences the strength of a binary acid: Molecular size: The larger the size of the non-hydrogen atom (X), the weaker the bond to hydrogen, making it easier to donate H+ and increasing acid strength. Electronegativity of X (the non-H element): Higher electronegativity pulls electron density away from the hydrogen, weakening the H-X bond and making the acid stronger. Binary acid: Oxoacid: Polyprotic Acid: Molecular size: Electronegativity of X (the non-H element): Stability of the conjugate base:
Chapter 14 Stability of the conjugate base: The more stable the conjugate base, the stronger the acid because the acid readily donates H+ without reforming. Fill in the blank: The stronger an acid is, the _ weaker __ its conjugate base is, and vice versa. Without looking up Kb values, which is the strongest base: F–, Cl–, Br–, or I–? Explain why. Fluoride (F–) is the strongest base because it has the smallest atomic radius, making it least stable as a conjugate base and more likely to accept a proton. Define each of the factors below, explain how each influences the strength of an acid, and indicate the relative importance of each factor: Resonance stability: If the conjugate base is stabilized by resonance, the acid is stronger because it more readily donates H+. Inductive Effect: Electronegative atoms near the acidic proton pull electron density away, weakening the bond and increasing acid strength. Try it yourself! Without looking up Ka values, rank the following acids in order of increasing strength: HClO 4 , HClO 3 , HBrO 4 , H 2 SO 4 , H 2 SO 3. H2SO3 < HClO3 < HBrO4 < H2SO4 < HClO Resonance stability: Inductive Effect:
Chapter 14 Read Section 14.5 “Polyprotic Acids”. Define each of the following terms: What general trend can be observed in the successive acid-dissociation constants (Ka1, Ka2, etc.) for a polyprotic acid? Give a molecular-level explanation for the observation. Monoprotic acid: An acid that donates only one proton per molecule. Diprotic acid: An acid that donates two protons per molecule. Triprotic acid: An acid that donates three protons per molecule. Stepwise (or “successive”) ionization: The process by which polyprotic acids lose protons one at a time, each step having a different Ka value. Reflect. On our Chapter 14 “muddy waters” Canvas forum, post at least one question you have about today’s pre-class material. The instructor will answer a subset of these questions at the beginning of class. If you do not have a question about the material up until this point, the forum lists alternate response prompts. Monoprotic acid: Diprotic acid: Triprotic acid: Stepwise (or “successive”) ionization: