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These flashcards cover key concepts related to calorimetry and thermodynamics for exam review.
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Calorimetry
The experimental technique for measuring heat flow for physical or chemical processes.
Calorimetry Equation
q = mcΔT, where q = heat (J), m = mass (g), c = specific heat capacity (J/g·°C), ΔT = temperature change (°C).
Coffee‑cup Calorimeter
An open calorimeter used at constant pressure to measure heat flow.
Bomb Calorimeter
A sealed calorimeter used at constant volume to measure heat flow.
Calorimeter Constant
C_cal; used to account for the calorimeter itself when calculating heat.
Hess’s Law
The total enthalpy change for a reaction is the same regardless of the path taken.
Enthalpy (H)
The sum of internal energy plus pressure-volume work; H = E + PV.
Sign of q for Endothermic Process
Positive (q > 0); indicates heat flows into the system.
First Law of Thermodynamics
ΔE = q + w, where ΔE is the change in internal energy, q is heat added, and w is work done.
Sign Convention for Work
Work (w) is negative if the system expands (ΔV > 0).
qp = ΔH
At constant pressure, the heat flow equals the enthalpy change.
qv = ΔE
At constant volume, the heat flow equals the change in internal energy.
Standard Enthalpy of Formation (ΔHf°)
Enthalpy change when 1 mol of a compound forms from its elements in standard states.
Calculating ΔHrxn°
ΔH_rxn° = Σn ΔHf°(products) - Σm ΔHf°(reactants).
Sign of q for Exothermic Process
Negative (q < 0); indicates heat flows out of the system.
Heat Capacities Relation
C = mc, where C is heat capacity (J/°C) and c is specific heat capacity per unit mass.
Expressing Δ(PV) for Ideal Gas
Δ(PV) = Δ(nRT) = R T Δn if temperature is constant.
Relation between ΔE and ΔH
ΔH = ΔE when there is no gas change (Δngas = 0).
Correcting for Calorimeter Heat Loss/Gain
In a multi-component system: qreaction + qwater + q_cal = 0.
To solve for q_reaction
Use measured ΔT and known mass (m), specific heat (c), and calorimeter constant (C_cal).