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ln(Rate) = m · ln([Fe³⁺]) + ln(constant)
Slopes typically round to whole numbers (such as 1 or 2)
Graph 1 (ln(Rate) vs. ln([Fe³⁺])): The slope equals the reaction order m with respect to Fe³⁺
Graph 2 (ln(Rate) vs. ln([I⁻])): The slope equals the reaction order n with respect to I⁻.
Because [H₂O] and [OH⁻] are in huge excess compared to [dye], their concentrations remain effectively constant, making the reaction behave as first-order with respect to the dye
Rate = k_obs[dye], where k_obs = k₁[H₂O] + k₂[OH⁻]
ln(Ksp) = (-ΔH° / R)(1 / T) + (ΔS° / R), where T is in Kelvin and R = 8.314 J/(K·mol)
On a graph of ln(Ksp) vs. 1/T, Slope = -ΔH° / R., ΔH° = -Slope × R.
ΔTf = i · Kf · m
ΔTf = Tf(solvent) - Tf(solution) (always expressed as a positive temperature drop).
Step-by-Step Molar Mass Calculation
Find ΔTf from cooling curves.
Calculate molality: m = ΔTf / (i · Kf).
Calculate moles of solute: Moles = m × kg of solvent.
Calculate molar mass: Molar Mass = Mass of solute (g) / Moles of solute.
1. Mass dissolved = Initial solid mass - Remaining solid mass after dissolution.
2. Moles dissolved = Mass dissolved / 261.34 g/mol.
3. Molarity (M) = Moles dissolved / 0.0500 L (for a 50.0 mL sample).
1. Mix KI, Na₂S₂O₃, starch indicator, and water, then add Fe(NO₃)₃ and start timing
2. Stop the timer when the solution turns dark blue-black to calculate the reaction rate
3. Repeat while varying [Fe³⁺] and [I⁻] separately, then use ln(Rate) vs. ln[reactant] plots to find the reaction orders
1. Mix phosphate buffer solutions to set [OH⁻] and add methyl green dye
2. Measure absorbance over time in a spectrophotometer as the green color fades
3. Plot −ln(A) vs. time to get k_obs, then plot k_obs vs. [OH⁻] across different buffers to get k₂
1. Saturate water with excess solid borax at several different temperatures
2. Pipet out a sample of the clear liquid (no solid) and titrate with HCl using bromocresol green to find molar solubility and Ksp
3. Plot ln(Ksp) vs. 1/T to calculate ΔH° from the slope
1. Measure the cooling curve of pure water in an ice-salt bath to find its normal freezing point
2. Dissolve a weighed solute in water and measure its new, lower freezing point
3. Use ΔTf to calculate molality, moles, and the solute's molar mass
1. Coat a conductive glass slide with TiO₂ paste, bake it, and soak it in raspberry juice (anthocyanin dye)
2. Coat a second conductive slide with carbon soot from a flame
3. Clamp both slides together with iodine electrolyte in between and measure voltage and current under light
1. Synthesis: React copper(II) sulfate with ammonia and ethanol, then vacuum-filter and dry the crystals
2. Analysis: Find mass percentages of sulfate (precipitate with BaCl₂), ammonia (titrate with HCl), and copper (absorbance via Beer's Law) to determine the empirical formula
1. Dilute a measured sample of vinegar with water and add phenolphthalein indicator
2. Titrate with standardized NaOH until a faint, permanent pink endpoint appears
3. Use M₁V₁ = M₂V₂ to find vinegar's molarity and convert to percent (w/v)
1. Place a calibrated pH probe in a measured sample of vinegar and record the initial pH
2. Add NaOH in small increments while recording pH to map the full titration curve
3. Use the steepest jump (equivalence point) to find molarity and the halfway-point pH to find pKa and Ka
1. Stir excess solid Ba(NO₃)₂ in distilled water until saturated, then decant off the liquid
2. Evaporate the remaining wet solid to dryness and weigh it to find how much dissolved, then calculate Ksp
3. Repeat using HNO₃ instead of water to observe lower solubility from the common ion effect
1. Prepare a dilute KSCN solution in HNO₃ and zero the spectrometer using HNO₃ as a blank
2. Add small, equal increments of Fe(NO₃)₃ to the beaker, measuring absorbance after each addition and returning the sample
3. Plot the linearized Beer's Law data and take the negative slope to find Keq