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How do we calculate the heat exchanged using specific heat capacity, and how does calorimetry measure it?

Topic 6.4 Heat Capacity and Calorimetry: use the equation q equals mc delta T with specific heat capacity, and use calorimetry data to determine the heat of a process.

A focused answer to AP Chemistry Topic 6.4, covering specific heat capacity, the equation q equals mc delta T, calorimetry, and how to determine the heat and enthalpy of a process from temperature data, with full worked examples.

Generated by Claude Opus 4.811 min answer

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  1. What this topic is asking
  2. Specific heat capacity and the heat equation
  3. Calorimetry
  4. From heat to enthalpy per mole
  5. Try this

What this topic is asking

The College Board (Topic 6.4) wants you to use the equation q=mcΔTq = mc\Delta T with specific heat capacity to calculate the heat exchanged, and to use calorimetry data to determine the heat (and hence enthalpy) of a process. This is the quantitative core of the thermodynamics unit: turning a measured temperature change into a quantity of energy.

Specific heat capacity and the heat equation

The specific heat capacity is the energy needed to raise the temperature of one gram of a substance by one degree Celsius (or kelvin). A large cc (like water's 4.18 J g1C14.18\ \text{J g}^{-1}\,^\circ\text{C}^{-1}) means the substance resists temperature change, absorbing a lot of heat for a small rise. This is why water is used as a coolant and why oceans moderate climate.

Calorimetry

A simple coffee-cup calorimeter is an insulated container of water in which a reaction occurs. You measure the temperature change of the water, compute qwater=mcΔTq_\text{water} = mc\Delta T, and infer the heat of the reaction as its negative. Dividing by the moles of the limiting reactant gives the molar enthalpy change ΔH\Delta H. The insulation assumption (no heat lost to the surroundings) is what allows the simple energy balance.

From heat to enthalpy per mole

For a reaction at constant pressure, the heat measured is the enthalpy change for the amount of substance reacted. To report a molar enthalpy, divide the total heat by the number of moles:

ΔH=qreactionn\Delta H = \frac{q_\text{reaction}}{n}

The sign follows the convention: an exothermic reaction warms the water (qwater>0q_\text{water} > 0), so qreaction<0q_\text{reaction} < 0 and ΔH<0\Delta H < 0. This links the laboratory measurement directly to the enthalpy of reaction defined in Topic 6.6.

Try this

Q1. Calculate the heat needed to raise 25.025.0 g of water by 10.0 C10.0\ ^\circ\text{C} (c=4.18 J g1C1c = 4.18\ \text{J g}^{-1}\,^\circ\text{C}^{-1}). [2 points]

  • Cue. q=(25.0)(4.18)(10.0)=1045 J1.05×103 Jq = (25.0)(4.18)(10.0) = 1045\ \text{J} \approx 1.05 \times 10^{3}\ \text{J}.

Q2. A reaction releases 2.0 kJ2.0\ \text{kJ} when 0.0200.020 mol reacts. Calculate ΔH\Delta H per mole. [2 points]

  • Cue. ΔH=2.0 kJ0.020 mol=100 kJ mol1\Delta H = \dfrac{-2.0\ \text{kJ}}{0.020\ \text{mol}} = -100\ \text{kJ mol}^{-1}.

Exam-style practice questions

Practice questions written in the style of College Board exam questions on this dot point, with worked answer explainers. The year tag is the paper they imitate, not the source.

AP 2023 (style)4 marksSection II (long FRQ, part). A 50.050.0 g sample of a metal at 100.0 C100.0\ ^\circ\text{C} is added to 100.0100.0 g of water at 24.0 C24.0\ ^\circ\text{C} in a calorimeter. The final temperature is 28.0 C28.0\ ^\circ\text{C}. The specific heat of water is 4.18 J g1C14.18\ \text{J g}^{-1}\,^\circ\text{C}^{-1}. (a) Calculate the heat gained by the water. (b) Determine the heat lost by the metal. (c) Calculate the specific heat capacity of the metal. (d) Justify why the calorimeter is assumed to be insulated.
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A 4-point quantitative FRQ on calorimetry.

(a) Heat gained by water (1 point): qwater=mcΔT=(100.0)(4.18)(28.024.0)=(100.0)(4.18)(4.0)=1672 J1.67×103 Jq_\text{water} = mc\Delta T = (100.0)(4.18)(28.0 - 24.0) = (100.0)(4.18)(4.0) = 1672\ \text{J} \approx 1.67 \times 10^{3}\ \text{J}.
(b) Heat lost by metal (1 point): qmetal=qwater=1.67×103 Jq_\text{metal} = -q_\text{water} = -1.67 \times 10^{3}\ \text{J} (the metal loses what the water gains).
(c) Specific heat of metal (1 point): ΔTmetal=28.0100.0=72.0 C\Delta T_\text{metal} = 28.0 - 100.0 = -72.0\ ^\circ\text{C}; c=qmΔT=1672(50.0)(72.0)=0.46 J g1C1c = \dfrac{q}{m\Delta T} = \dfrac{-1672}{(50.0)(-72.0)} = 0.46\ \text{J g}^{-1}\,^\circ\text{C}^{-1}.
(d) Justify (1 point): assuming no heat escapes lets us set qmetal=qwaterq_\text{metal} = -q_\text{water}; an insulated calorimeter ensures the only heat exchange is between the metal and the water.

Markers reward the heat into water, equating it to the heat from the metal, the metal's specific heat, and the insulation assumption.

AP 2021 (style)1 marksSection I (multiple choice). Equal masses of water and aluminum absorb the same quantity of heat. Water (c=4.18c = 4.18) has a higher specific heat than aluminum (c=0.90 J g1C1c = 0.90\ \text{J g}^{-1}\,^\circ\text{C}^{-1}). The temperature rise is (A) greater for water (B) greater for aluminum (C) equal for both (D) zero for both. Justify your choice.
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A 1-point conceptual MCQ. The answer is (B).

From q=mcΔTq = mc\Delta T, with qq and mm fixed, ΔT=qmc\Delta T = \dfrac{q}{mc} is inversely proportional to cc. Aluminum has the smaller specific heat, so it has the larger temperature rise. The trap is assuming the same heat gives the same temperature change regardless of cc.

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