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Questions and Answers
What is the characteristic of strong acids regarding their contribution to hydronium ion concentration?
What is the characteristic of strong acids regarding their contribution to hydronium ion concentration?
For a monoprotic strong acid, how do the concentrations of hydronium ions and the acid compare?
For a monoprotic strong acid, how do the concentrations of hydronium ions and the acid compare?
How does the ionization of weak acids generally compare in water?
How does the ionization of weak acids generally compare in water?
What occurs during the endpoint of an acid-base titration?
What occurs during the endpoint of an acid-base titration?
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What is the significance of the inflection point on a titration curve?
What is the significance of the inflection point on a titration curve?
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In a titration setup, what is the role of the indicator?
In a titration setup, what is the role of the indicator?
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Which of the following statements about weak acids is correct?
Which of the following statements about weak acids is correct?
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Which of the following does not typically describe strong acids?
Which of the following does not typically describe strong acids?
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What defines a strong electrolyte in an aqueous solution?
What defines a strong electrolyte in an aqueous solution?
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At 25 °C, what is the concentration of hydroxide ions in a solution that has a hydronium ion concentration of $1.0 imes 10^{-3}$ M?
At 25 °C, what is the concentration of hydroxide ions in a solution that has a hydronium ion concentration of $1.0 imes 10^{-3}$ M?
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What is the pH of a solution with a hydronium ion concentration of $0.001$ M?
What is the pH of a solution with a hydronium ion concentration of $0.001$ M?
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Which of the following statements is correct about acidic and basic solutions?
Which of the following statements is correct about acidic and basic solutions?
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What is the relationship between pH and pOH at 25 °C?
What is the relationship between pH and pOH at 25 °C?
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Which of the following describes a neutral solution?
Which of the following describes a neutral solution?
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What occurs in an aqueous solution of a strong acid?
What occurs in an aqueous solution of a strong acid?
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Which of these factors does NOT affect the pH of a solution?
Which of these factors does NOT affect the pH of a solution?
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Which of the following definitions of acids and bases is the most restrictive?
Which of the following definitions of acids and bases is the most restrictive?
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In the context of the Arrhenius concept, what do acids produce when dissolved in water?
In the context of the Arrhenius concept, what do acids produce when dissolved in water?
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What do bases produce in aqueous solution under the Arrhenius definition?
What do bases produce in aqueous solution under the Arrhenius definition?
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According to the Brønsted–Lowry definition, which statement is true about acids?
According to the Brønsted–Lowry definition, which statement is true about acids?
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What distinguishes the Lewis definition of acids and bases from the other definitions?
What distinguishes the Lewis definition of acids and bases from the other definitions?
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What happens during an Arrhenius acid-base reaction?
What happens during an Arrhenius acid-base reaction?
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Which of the following statements accurately describes the interaction of an acid and a base?
Which of the following statements accurately describes the interaction of an acid and a base?
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What is the result of mixing a strong acid with a strong base?
What is the result of mixing a strong acid with a strong base?
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What does the solubility product constant (Ksp) represent?
What does the solubility product constant (Ksp) represent?
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To compare the Ksp values of two ionic compounds, what must be true?
To compare the Ksp values of two ionic compounds, what must be true?
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How is molar solubility defined?
How is molar solubility defined?
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What occurs when a solid ionic compound is placed in a saturated solution?
What occurs when a solid ionic compound is placed in a saturated solution?
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Given the dissolution of lead(II) iodide (PbI2), how does the molar solubility relate to its Ksp?
Given the dissolution of lead(II) iodide (PbI2), how does the molar solubility relate to its Ksp?
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What is the general form of the solubility product expression for an ionic compound MLn?
What is the general form of the solubility product expression for an ionic compound MLn?
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If 1.2 x $10^{-3}$ mol of PbI2 dissolves in 1 L of solution, what is a likely implication about its Ksp?
If 1.2 x $10^{-3}$ mol of PbI2 dissolves in 1 L of solution, what is a likely implication about its Ksp?
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Why are some ionic compounds considered insoluble?
Why are some ionic compounds considered insoluble?
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How does the addition of a soluble salt affect the solubility of a slightly soluble salt?
How does the addition of a soluble salt affect the solubility of a slightly soluble salt?
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What happens when the ion product Q exceeds the solubility product Ksp?
What happens when the ion product Q exceeds the solubility product Ksp?
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In fractional precipitation, what is essential for successfully separating cations?
In fractional precipitation, what is essential for successfully separating cations?
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What is the relationship between the molar solubility of calcium oxalate and the addition of calcium chloride?
What is the relationship between the molar solubility of calcium oxalate and the addition of calcium chloride?
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How is the ion product Q calculated for a solubility reaction?
How is the ion product Q calculated for a solubility reaction?
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What describes the condition when a solution is saturated regarding precipitation?
What describes the condition when a solution is saturated regarding precipitation?
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What will occur if the concentration of ions exceeds their respective solubility product in a solution?
What will occur if the concentration of ions exceeds their respective solubility product in a solution?
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Why is the common-ion effect significant in solubility equilibria?
Why is the common-ion effect significant in solubility equilibria?
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Which cation will be reduced first at the cathode when multiple cations are present?
Which cation will be reduced first at the cathode when multiple cations are present?
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What is the role of the anode in an electrolytic cell?
What is the role of the anode in an electrolytic cell?
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How is the amount of product formed in an electrolytic cell related to electron transfer?
How is the amount of product formed in an electrolytic cell related to electron transfer?
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What does Faraday’s constant represent in electrolysis?
What does Faraday’s constant represent in electrolysis?
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Which of the following statements best describes the flow of electrons in an electrochemical cell?
Which of the following statements best describes the flow of electrons in an electrochemical cell?
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What must be calculated to determine the moles of metal deposited in an electrolysis reaction?
What must be calculated to determine the moles of metal deposited in an electrolysis reaction?
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What is the standard cell potential ($E°_{cell}$) for the given reaction involving copper and zinc?
What is the standard cell potential ($E°_{cell}$) for the given reaction involving copper and zinc?
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In a spontaneous oxidation-reduction reaction, which statement is true regarding Gibbs free energy ($ riangle G°$)?
In a spontaneous oxidation-reduction reaction, which statement is true regarding Gibbs free energy ($ riangle G°$)?
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What effect does increasing the concentration of reactants have on the cell potential according to the Nernst equation?
What effect does increasing the concentration of reactants have on the cell potential according to the Nernst equation?
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Which electrode is associated with the reduction half-reaction in a voltaic cell?
Which electrode is associated with the reduction half-reaction in a voltaic cell?
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What is the relationship between equilibrium constant (K) and standard cell potential ($E°_{cell}$) for a spontaneous reaction?
What is the relationship between equilibrium constant (K) and standard cell potential ($E°_{cell}$) for a spontaneous reaction?
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How does the presence of oxygen typically affect the corrosion of metals?
How does the presence of oxygen typically affect the corrosion of metals?
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What does the Nernst equation indicate about cell potential ($E_{cell}$) as temperature increases?
What does the Nernst equation indicate about cell potential ($E_{cell}$) as temperature increases?
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What is the standard reduction potential (E°red) for the reduction of O2 in moist conditions?
What is the standard reduction potential (E°red) for the reduction of O2 in moist conditions?
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What occurs at the cathode during electrolysis?
What occurs at the cathode during electrolysis?
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Which of the following reactions represents the anode reaction during the electrolysis of water?
Which of the following reactions represents the anode reaction during the electrolysis of water?
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In electrolysis, what type of material is typically used as electrodes?
In electrolysis, what type of material is typically used as electrodes?
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During electrolysis, what is the role of the electrolyte?
During electrolysis, what is the role of the electrolyte?
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What must be true for the electrolysis of a pure compound to occur successfully?
What must be true for the electrolysis of a pure compound to occur successfully?
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Which statement correctly describes the electroplating process?
Which statement correctly describes the electroplating process?
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Which of the following best describes the process of electrolysis?
Which of the following best describes the process of electrolysis?
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What does E° represent in the context of half-reactions during electrolysis?
What does E° represent in the context of half-reactions during electrolysis?
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What plays a crucial role in determining the rate of a chemical reaction according to Collision Theory?
What plays a crucial role in determining the rate of a chemical reaction according to Collision Theory?
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Which factor does NOT directly affect the rate constant (k) for a reaction?
Which factor does NOT directly affect the rate constant (k) for a reaction?
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In the context of reaction mechanisms, how is the rate-determining step best characterized?
In the context of reaction mechanisms, how is the rate-determining step best characterized?
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What is the relationship between activation energy and the rate of a chemical reaction?
What is the relationship between activation energy and the rate of a chemical reaction?
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Which of the following best explains the impact of a catalyst on a chemical reaction?
Which of the following best explains the impact of a catalyst on a chemical reaction?
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Which characteristic is true regarding effective collisions in the context of chemical reactions?
Which characteristic is true regarding effective collisions in the context of chemical reactions?
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What happens to the rate constant when the temperature of a reaction increases?
What happens to the rate constant when the temperature of a reaction increases?
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In a two-point form of the Arrhenius equation, what does the variable Ea represent?
In a two-point form of the Arrhenius equation, what does the variable Ea represent?
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What is the role of the activated complex in a chemical reaction?
What is the role of the activated complex in a chemical reaction?
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Why do more complex reactant molecules result in less frequent effective collisions?
Why do more complex reactant molecules result in less frequent effective collisions?
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Which statement best describes the rate-determining step in a reaction mechanism?
Which statement best describes the rate-determining step in a reaction mechanism?
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How do catalysts affect reaction mechanisms?
How do catalysts affect reaction mechanisms?
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What characterizes the elementary reactions in a reaction mechanism?
What characterizes the elementary reactions in a reaction mechanism?
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What is the effect of activation energy on the rate of a reaction?
What is the effect of activation energy on the rate of a reaction?
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In a reaction mechanism, what is the significance of reaction intermediates?
In a reaction mechanism, what is the significance of reaction intermediates?
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What can be inferred about the probability of simultaneous collisions involving more than three molecules?
What can be inferred about the probability of simultaneous collisions involving more than three molecules?
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How does the half-life of a second order reaction change with increasing initial concentration?
How does the half-life of a second order reaction change with increasing initial concentration?
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What does the Arrhenius equation indicate about the relationship between the rate constant and temperature?
What does the Arrhenius equation indicate about the relationship between the rate constant and temperature?
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Which statement accurately describes the activation energy in the context of a chemical reaction?
Which statement accurately describes the activation energy in the context of a chemical reaction?
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What is true about the transition state or activated complex during a chemical reaction?
What is true about the transition state or activated complex during a chemical reaction?
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When considering the effect of a catalyst on a reaction, what statement is correct?
When considering the effect of a catalyst on a reaction, what statement is correct?
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In an energy profile for a reaction, what does the difference in energy between reactants and the activated complex represent?
In an energy profile for a reaction, what does the difference in energy between reactants and the activated complex represent?
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What effect does increasing the concentration of reactants have on the rate of a second order reaction?
What effect does increasing the concentration of reactants have on the rate of a second order reaction?
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Which factor primarily determines the rate at which a reactant approaches the activation energy?
Which factor primarily determines the rate at which a reactant approaches the activation energy?
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Study Notes
Strong Acids and Bases
- Water's contribution to [H3O+] or [OH−] is negligible in strong acids or bases due to high concentration.
- Six strong acids: Five are monoprotic (HCl, HBr, HI, HClO4, HNO3) and one diprotic (H2SO4).
- For monoprotic strong acids, [H3O+] equals acid concentration: [H3O+] = [HAcid], e.g., 0.10 M HCl yields [H3O+] = 0.10 M and pH = 1.00.
Weak Acids
- Weak acids ionize partially in water, typically < 1%.
- The relationship [H3O+] < [acid] is common, indicating weak acids donate few hydrogens compared to their total concentration.
- Buffers require higher concentrations of weak acid ([acid] > [base]) to maintain effectiveness with added base.
Titration
- Titration involves adding titrant to a known concentration solution until the reaction reaches completion, signaled by an endpoint.
- An indicator may be added to identify the endpoint through color change.
- Titration is complete when moles of H3O+ equals moles of OH− (equivalence point).
- Titration curve plots pH against the amount of titrant; the inflection point marks the equivalence point.
Solutions of Strong Acids and Bases
- Aqueous solutions of strong acids and bases contain both H3O+ and OH– ions.
- Neutral solutions have equal concentrations of [H3O+] and [OH–] (1.00 × 10−7 M).
- Acidic solutions have [H3O+] > 1.00 × 10−7 M, while basic solutions have [OH–] > 1.00 × 10−7 M.
pH and pOH
- pH indicates the acidity/basicity of a solution, calculated as pH = – log[H3O+].
- pH < 7 denotes acidity, pH > 7 denotes basicity, and pH = 7 denotes neutrality, with a typical range of 0 to 14.
- pOH can be derived similarly to pH; the relationship is defined by the equation pH + pOH = 14.
Sources of Ions
- In strong acid solutions, both the acid and water contribute to [H3O+].
- In strong base solutions, [OH−] arises from both the base and water.
Acid and Base Definitions
- Arrhenius: Acids produce H3O+, bases produce OH−.
- Bronsted-Lowry: Acids donate H3O+; bases accept H3O+.
- Lewis: Acids accept electron pairs; bases donate electron pairs.
Chemical Reactions
- Arrhenius acids yield H+ in solution (e.g., HCl dissociates to H+ and Cl−).
- Arrhenius bases yield OH− in solution (e.g., NaOH dissociates to Na+ and OH−).
- In acid-base reactions, H+ from the acid combines with OH− from the base to form water (H2O), while the remaining ions form a salt.
Solubility and Common-Ion Effect
- The presence of a soluble salt with a common ion decreases the solubility of a slightly soluble salt, shifting the equilibrium left.
- Example: Adding Pb(NO3)2 to PbCrO4 decreases the solubility of PbCrO4.
Molar Solubility Example
- Molar solubility of calcium oxalate in a 0.15 M calcium chloride solution can be calculated using its solubility product of 2.3 x 10^-9.
Precipitation Process
- Precipitation occurs when ion concentrations exceed the ionic compound's solubility.
- Determining precipitation involves comparing the ion product (Q) to the solubility product constant (Ksp):
- Q = Ksp: Solution is saturated; no precipitation.
- Q < Ksp: Solution is unsaturated; no precipitation.
- Q > Ksp: Solution is supersaturated; precipitation occurs.
Fractional Precipitation
- Technique for separating ions by selectively precipitating them with a reagent that forms an insoluble salt.
- Effective if the Ksp values of the ions are significantly different.
Solubility Equilibria
- All ionic compounds have some degree of solubility in water, but some are classified as insoluble due to low solubility levels.
- The solubility equilibrium concepts enable the determination of relative solubilities using the equilibrium constant Ksp.
Solubility Product Constant (Ksp)
- Ksp is the equilibrium constant for the solubility of slightly soluble ionic compounds.
- The expression for Ksp can be represented as:
- M𝑝 X𝑞 𝑠 ⇌ 𝑝M 𝑚+ 𝑎𝑞 + 𝑞X 𝑛− 𝑎𝑞
- Ksp = [𝑀𝑚+]^p [𝑋𝑛−]^q
Molar Solubility (s)
- Molar solubility refers to the moles of solute dissolving in one liter of saturated solution.
- Molar solubility is directly related to Ksp, but Ksp comparisons are valid only for compounds with identical dissociation stoichiometries.
Example Calculations
- Residue from evaporated saturated calcium oxalate solution yields a mass of 0.0061 g; this can be used to find molar solubility.
- For lead(II) iodide (PbI2) with a solubility of 1.2 x 10^-3 mol in 1 L at 298 K, its Ksp can be calculated.
Anode and Cathode Reactions
- Anode oxidizes and replaces metal cations in the solution.
- At the cathode, the easiest cation to reduce (least negative or most positive E°red) is reduced first.
- At the anode, the easiest anion to oxidize (least negative or most positive E°ox) is oxidized first.
Stoichiometry of Electrolysis
- The amount of product generated in an electrolytic cell is directly related to the number of electrons transferred.
- Current and time dictate the flow of moles of electrons:
- 1 amp = 1 coulomb/second
- 1 mole of electrons = 96,485 coulombs (Faraday's constant).
- Conceptual flow in calculation: time (s) → coulombs → moles of electrons → moles of metal → grams of metal.
Example Reaction
- Cu(s) + Zn²⁺(aq) → Cu²⁺(aq) + Zn(s) indicating a nonspontaneous reaction.
- Reduction half-reactions:
- Cu²⁺(aq) + 2 e⁻ → Cu(s) with E°red = +0.34 V
- Zn²⁺(aq) + 2 e⁻ → Zn(s) with E°red = −0.76 V
Cell Potential and Spontaneity
- For spontaneous reactions: ΔG° is negative, E° is positive, and K > 1.
- Relationship: ΔG° = −RT ln K = −nFE°cell, where n is the number of electrons and F is Faraday’s constant.
Concentration and Cell Potential
- Nernst Equation: ΔG = ΔG° + RT ln Q
- Rearranged form: Ecell = E°cell - (RT/nF) ln Q.
- At 25 °C, converting from ln to log gives: Ecell = E°cell - (0.0592 V/n) log Q.
Corrosion
- Corrosion is the spontaneous oxidation of metals, primarily reacting with O₂.
- Active metals are especially prone to corrosion, which diminishes their strength and malleability.
- Corrosion products often flake off, allowing further oxidation of the underlying metal.
Reduction of O₂
- In moist conditions, O₂ can readily be reduced: O₂(g) + 2 H₂O(l) + 4 e⁻ → 2 OH⁻(aq), E° = 0.40 V.
- O₂ is more easily reduced in acidic conditions, facilitating various reactions.
Applications of Electrolysis
- Metal extraction and purification from ores.
- Production of hydrogen for fuel cells.
- Metal plating processes.
Electrolytic Cells
- Powered by a battery or DC source; anode is connected to the positive terminal, cathode to the negative.
- Electrolyte can be aqueous salt solution or molten ionic salt.
- Cations migrate to cathode for reduction, anions to anode for oxidation.
Electrolysis Reactions
- Possible cathode reactions include:
- Reduction of cation to metal.
- Reduction of water to hydrogen gas.
- Possible anode reactions include:
- Oxidation of anion to element.
- Oxidation of water to oxygen.
Electrolysis of Pure Compounds
- Requires molten state for compounds with electrodes typically made of graphite.
- Cations reduce to metal elements at the cathode while anions oxidize to nonmetal elements at the anode.
Electroplating
- In electroplating, the workpiece functions as the cathode where cations deposit onto its surface.
- The anode is composed of the metal being used for plating.
Reaction Order and Half-Life
- For a first-order reaction, half-life (t₁/₂) is directly proportional to the rate constant (k): t₁/₂ = 0.693/k.
- In a second-order reaction, half-life is inversely proportional to the initial concentration: t₁/₂ = 1/(k[A]₀).
- Increasing initial concentration results in a shorter half-life for second-order reactions.
Temperature Effects on Reaction Rates
- The rate constant (k) changes with temperature.
- The Arrhenius equation relates k to temperature (T), activation energy (Ea), and frequency factor (A): k = A * e^(-Ea/RT).
- T is measured in Kelvin, R is the gas constant (8.314 J/(K·mol)), and Ea represents the energy required to initiate reaction.
Activation Energy
- Activation energy is the energy barrier needed to form an activated complex from reactants.
- The activated complex, or transition state, contains partially formed and broken bonds, and has high energy.
- The energy difference between reactants and activated complex represents the activation energy.
Reaction Profile and Isomerization
- The energy profile for reactions, like the isomerization of methyl isonitrile, shows activation energy as the energy difference between the reactants and the activated complex.
- A graph of ln(k) vs. (1/T) is linear, signifying that as temperature increases, the rate constant also increases.
Two-Point Form of Arrhenius Equation
- To find the activation energy (Ea) with two data points (T, k), use: ln(k₂/k₁) = (-Ea/R)(1/T₁ - 1/T₂).
Collision Theory
- Reaction rates are influenced by collision theory, which states that reactants must collide with sufficient energy and correct orientation.
- Activation energy is the minimum energy required for a reaction to occur.
- The rate constant (k) depends on collision frequency, fraction of high-energy collisions, and proper orientation of reactants.
Effective Collisions
- Effective collisions must overcome the energy barrier to form the activated complex.
- Collision frequency increases the likelihood of effective collisions, thus increasing reaction rate.
Orientation Factor
- Proper orientation of reacting molecules is crucial for successful collisions, as it allows for bond breaking and formation.
- More complex molecules have lower probabilities for proper orientation during collisions.
Reaction Mechanisms
- A chemical reaction is often broken down into a series of elementary steps, called reaction mechanisms, derived from the overall net equation.
- The likelihood of simultaneous collisions involving more than three molecules is low; thus, most reactions involve one to three molecules at a time.
Example of a Reaction Mechanism
- For the overall reaction: H₂(g) + 2 ICl(g) → 2 HCl(g) + I₂(g), the mechanism includes:
- Elementary reaction 1: H₂(g) + ICl(g) → HCl(g) + HI(g).
- Elementary reaction 2: HI(g) + ICl(g) → HCl(g) + I₂(g).
- HI is a reaction intermediate, produced in step one and consumed in step two, hence it does not appear in the overall reaction.
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Description
This quiz focuses on the properties of strong acids and their influence on pH calculations. It covers key concepts related to hydronium ion concentration and the characteristics of monoprotic and diprotic acids. Test your knowledge on determining pH for strong acid solutions.