Química Inorgánica — Avanzado (C1/C2) 4: Chemical Kinetics, Equilibrium, Electrochemistry & Organic Functional Groups
[Español] Química Inorgánica: Reaction rates, rate laws, Le Chatelier's principle, equilibrium constants, galvanic/electrolytic cells, and organic functional groups
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- Química Inorgánica — Avanzado (C1/C2) 4: Chemical Kinetics, Equilibrium, Electrochemistry & Organic Functional Groups (.md)
Flashcards (32)
| # | Front (Term / Question) | Back (Definition / Answer) | Example | Multiple-Choice Options |
|---|---|---|---|---|
| 1 | How is the standard cell potential (E°cell) calculated from standard reduction potentials (E°red)? | E°cell = E°red(cathode) - E°red(anode). A positive E°cell denotes a thermodynamically spontaneous reaction. | ||
| 2 | Write the Nernst equation for calculating non-standard cell potential (Ecell). | Ecell = E°cell - (R*T / (n*F)) * ln(Q) = E°cell - (0.0592 V / n) * log10(Q) at 298 K. | ||
| 3 | What condition involving ion product (Qsp) and solubility product (Ksp) indicates that a precipitate will form? | A precipitate forms when Qsp > Ksp (supersaturated solution). | ||
| 4 | What products are obtained by oxidizing a primary alcohol versus a secondary alcohol with strong oxidizing agents (e.g., KMnO4 or Jones reagent)? | Primary alcohols are oxidized to carboxylic acids (via aldehyde intermediates); secondary alcohols are oxidized to ketones (tertiary alcohols resist oxidation). | ||
| 5 | What is the role of a salt bridge in a galvanic (voltaic) cell? | To maintain electrical neutrality by permitting spectator anions to migrate toward the anode and cations toward the cathode, preventing charge buildup. | ||
| 6 | What functional group results from the condensation reaction between a carboxylic acid derivative and an amine? | An amide bond (-CO-NRR'). | ||
| 7 | According to Le Chatelier's principle, how does increasing system pressure by decreasing volume affect a gaseous equilibrium? | The equilibrium shifts toward the side of the balanced equation with fewer total moles of gas to relieve the pressure. | ||
| 8 | What chemical transformation occurs during Fischer esterification? | A carboxylic acid reacts with an alcohol in the presence of an acid catalyst to produce an ester and water via nucleophilic acyl substitution. | ||
| 9 | What are the units of the rate constant (k) for zero-order, first-order, and second-order chemical reactions? | Zero-order: M/s (mol/(L*s)); First-order: s^-1; Second-order: M^-1 * s^-1 (L/(mol*s)). | ||
| 10 | What is the common ion effect on salt solubility? | The solubility of a sparingly soluble salt is markedly decreased in the presence of a soluble second salt that shares a common ion, driven by Le Chatelier's shift. | ||
| 11 | How does raising the temperature affect the equilibrium constant (K) for an exothermic reaction versus an endothermic reaction? | For an exothermic reaction (heat as product), increasing T decreases K (shifts left); for an endothermic reaction (heat as reactant), increasing T increases K (shifts right). | ||
| 12 | How does comparing the reaction quotient (Q) to the equilibrium constant (K) predict the direction of net reaction? | If Q < K, forward reaction proceeds (shifts right); if Q = K, system is at equilibrium; if Q > K, reverse reaction proceeds (shifts left). | ||
| 13 | What is the general differential rate law for a reaction aA + bB -> products, and how are reaction orders determined? | Rate = k[A]^m[B]^n, where m and n are reaction orders with respect to A and B, determined strictly experimentally (not from stoichiometric coefficients). | ||
| 14 | Which plotted variables yield a straight line for zero-order, first-order, and second-order integrated rate laws? | Zero-order: [A] vs t (slope = -k); First-order: ln[A] vs t (slope = -k); Second-order: 1/[A] vs t (slope = +k). | ||
| 15 | What thermodynamic equation relates standard Gibbs free energy change (ΔG°) to standard cell potential (E°cell)? | ΔG° = -n * F * E°cell, where n is moles of transferred electrons and F is Faraday's constant (96,485 C/mol e-). | ||
| 16 | What defines an electrophile versus a nucleophile in organic reaction mechanisms? | An electrophile is an electron-deficient species (Lewis acid) seeking electron density; a nucleophile is an electron-rich species with a lone pair or pi bond (Lewis base) that donates electrons to form a bond. | ||
| 17 | What is dynamic chemical equilibrium, and what is true regarding forward and reverse reaction rates? | A closed system state where the rates of forward and reverse reactions are equal (rf = rr), resulting in constant macroscopic concentrations over time. | ||
| 18 | What defines aromaticity in planar cyclic conjugated molecules according to Hückel's rule? | The ring must be cyclic, planar, fully conjugated with a continuous ring of p-orbitals, and contain (4n + 2) pi electrons (where n is a non-negative integer: 2, 6, 10, 14...). | ||
| 19 | What structural feature distinguishes an aldehyde from a ketone? | Both contain a carbonyl group (C=O); an aldehyde has the carbonyl bonded to at least one hydrogen atom (terminal R-CHO), while a ketone has the carbonyl bonded to two carbon groups (internal R-CO-R'). | ||
| 20 | What defines a chiral center (stereocenter) in an organic molecule? | An sp3-hybridized tetrahedral carbon atom bonded to four chemically distinct substituent groups. | ||
| 21 | What is the rate-determining step (RDS) in a multi-step reaction mechanism? | The slowest elementary step with the highest activation energy barrier, which dictates the overall reaction rate and rate law. | ||
| 22 | What is the relationship between enantiomers and diastereomers in stereochemistry? | Enantiomers are non-superimposable mirror-image stereoisomers with identical physical properties except optical rotation; diastereomers are stereoisomers that are not mirror images and possess different physical and chemical properties. | ||
| 23 | What thermodynamic equation connects standard cell potential (E°cell) to the equilibrium constant (K) at 298.15 K? | E°cell = (R*T / (n*F)) * ln(K) = (0.0592 V / n) * log10(K). | ||
| 24 | Write the Arrhenius equation and identify all variables and physical constants. | k = A * exp(-Ea / (R*T)), where k is rate constant, A is pre-exponential frequency factor, Ea is activation energy, R is gas constant (8.314 J/(mol*K)), and T is temperature in Kelvin. | ||
| 25 | How does a chemical catalyst accelerate a reaction without being consumed? | It provides an alternative reaction pathway with a lower activation energy (Ea), increasing rate constants of both forward and reverse reactions equally. | ||
| 26 | How do galvanic cells and electrolytic cells differ in spontaneity and external energy requirements? | Galvanic cells produce electrical energy spontaneously from chemical reactions (ΔG < 0, Ecell > 0); electrolytic cells consume external electrical voltage to drive non-spontaneous reactions (ΔG > 0, Ecell < 0). | ||
| 27 | Why are aliphatic amines basic and nucleophilic in organic reactions? | The nitrogen atom possesses a non-bonding lone pair of electrons available to accept a proton (Brønsted base) or attack electrophilic centers (Lewis base/nucleophile). | ||
| 28 | How are primary (1°), secondary (2°), and tertiary (3°) alcohols classified structurally? | By the number of carbon atoms bonded to the carbinol carbon carrying the -OH group: 1° is bonded to one carbon, 2° to two carbons, and 3° to three carbons. | ||
| 29 | What is the solubility product constant (Ksp) expression for the dissolution of silver chromate, Ag2CrO4(s) <-> 2 Ag+(aq) + CrO4^2-(aq)? | Ksp = [Ag+]^2 * [CrO4^2-], with solids omitted from mass action expressions. | ||
| 30 | What is the relationship between the equilibrium constants Kc and Kp for an ideal gas reaction? | Kp = Kc * (R*T)^Δn, where Δn = (moles of gaseous products) - (moles of gaseous reactants), and R = 0.08206 L*atm/(mol*K). | ||
| 31 | What is the half-life equation for a first-order chemical reaction, and why is it unique? | t_1/2 = ln(2) / k ≈ 0.693 / k; it is completely independent of the initial reactant concentration [A]0. | ||
| 32 | In an electrochemical cell, which electrode is the site of oxidation, and which is the site of reduction? | Oxidation always occurs at the anode (An Ox); reduction always occurs at the cathode (Red Cat). |