Thermochemistry Lecture and Practice Examination Review

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Vocabulary practice flashcards covering calorimetry, molar enthalpies of combustion, formation, and reaction, Hess's Law, and energetic states from thermochemistry lecture problems.

15 Terms

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Thermal Mixing Equilibrium Temperature

The resultant equilibrium temperature reached when heat transfer occurs between two thermal masses without loss to the container or surroundings; for example, mixing 150 g150\,\text{g} of water at 75∘C75^\circ\text{C} with 75 g75\,\text{g} of water at 20∘C20^\circ\text{C} results in a final temperature of 57∘C57^\circ\text{C}.

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Specific Heat Capacity of Nickel (cNic_{\text{Ni}})

The quantity of heat required to raise the temperature of one gram of nickel by one degree Celsius, specified as 0.444 J/(g⋅∘C)0.444\,\text{J}/(\text{g}\cdot^\circ\text{C}).

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Specific Heat Capacity of Steam (csteamc_{\text{steam}})

The quantity of heat required to change the temperature of gaseous water per unit mass, given as 2.02 J/(g⋅∘C)2.02\,\text{J}/(\text{g}\cdot^\circ\text{C}); cooling 145 g145\,\text{g} of steam from 140∘C140^\circ\text{C} to 124∘C124^\circ\text{C} requires the removal of 4.69 kJ4.69\,\text{kJ} of energy.

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Molar Heat of Combustion of Diethylamine

The enthalpy change when one mole of diethylamine, (C2H5)2NH(\text{C}_2\text{H}_5)_2\text{NH}, undergoes complete combustion, defined as 3003.811 kJ/mol3003.811\,\text{kJ/mol}, resulting in the release of 2.05 MJ2.05\,\text{MJ} (or 2053 kJ2053\,\text{kJ}) when burning a 50.0 g50.0\,\text{g} sample.

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Molar Heat of Combustion of Glucose

The standard enthalpy change for the complete combustion of glucose according to the equation C6H12O6(g)+6O2(g)→6CO2(g)+6H2O(l)\text{C}_6\text{H}_{12}\text{O}_6(g) + 6\text{O}_2(g) \rightarrow 6\text{CO}_2(g) + 6\text{H}_2\text{O}(l), calculated using molar heats of formation as −2802.5 kJ/mol-2802.5\,\text{kJ/mol}.

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Molar Heat of Formation of Ethene (ΔfHm\Delta_f H_m)

The standard molar enthalpy of formation of C2H4(g)\text{C}_2\text{H}_4(g), determined to be +52.4 kJ/mol+52.4\,\text{kJ/mol} using its combustion reaction: C2H4(g)+3O2(g)→2CO2(g)+2H2O(g)\text{C}_2\text{H}_4(g) + 3\text{O}_2(g) \rightarrow 2\text{CO}_2(g) + 2\text{H}_2\text{O}(g) with ΔcHm=−1322.9 kJ/mol\Delta_c H_m = -1322.9\,\text{kJ/mol}.

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Enthalpy of Combustion of Hydrazine (ΔcHm\Delta_c H_m)

The molar enthalpy of reaction for N2H4(g)+3O2(g)→2H2O(g)+2NO2(g)\text{N}_2\text{H}_4(g) + 3\text{O}_2(g) \rightarrow 2\text{H}_2\text{O}(g) + 2\text{NO}_2(g), which equals −4.00×102 kJ/mol-4.00 \times 10^2\,\text{kJ/mol}, yielding 40.0 kJ40.0\,\text{kJ} of released energy when 3.60 g3.60\,\text{g} of H2O(g)\text{H}_2\text{O}(g) is formed.

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Enthalpy Change of Sodium Oxide Hydration

The heat released in the reaction Na2O(s)+H2O(l)→2NaOH(s)\text{Na}_2\text{O}(s) + \text{H}_2\text{O}(l) \rightarrow 2\text{NaOH}(s), where ΔH=−168 J\Delta H = -168\,\text{J}; producing 21 J21\,\text{J} of energy corresponds to the formation of 1.0×101 g1.0 \times 10^1\,\text{g} of NaOH(s)\text{NaOH}(s).

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Enthalpy of Reaction for Sodium and Phosphoric Acid (ΔrH\Delta_r H)

The net heat of reaction for 6Na(s)+2H3PO4(aq)→3H2(g)+2Na3PO4(aq)6\text{Na}(s) + 2\text{H}_3\text{PO}_4(aq) \rightarrow 3\text{H}_2(g) + 2\text{Na}_3\text{PO}_4(aq), determined to be −1.80×102 kJ-1.80 \times 10^2\,\text{kJ} based on the release of 30.0 kJ30.0\,\text{kJ} of energy when 1.010 g1.010\,\text{g} of H2(g)\text{H}_2(g) is produced.

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Molar Heat of Oxidation of Sucrose

The enthalpy released per mole of sucrose oxidized in the human body at 37∘C37^\circ\text{C} (assuming H2O\text{H}_2\text{O} is formed), calculated as −3.77 MJ/mol-3.77\,\text{MJ/mol} from data showing that 30.0 g30.0\,\text{g} of sucrose provides 0.330 MJ0.330\,\text{MJ} of energy.

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Molar Heat of Combustion of Ammonia

The predicted enthalpy of combustion for NH3(g)\text{NH}_3(g) to form NO(g)\text{NO}(g) and H2O(g)\text{H}_2\text{O}(g), calculated via Hess's Law from component formation equations to be −226.4 kJ/mol-226.4\,\text{kJ/mol}.

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Stored Energy in Water Systems

The comparative total internal thermal energy contained within water phases, in which 1.0 mole1.0\,\text{mole} of H2O(g)\text{H}_2\text{O}(g) at 100∘C100^\circ\text{C} stores more energy than 1.0 mole1.0\,\text{mole} of H2O(l)\text{H}_2\text{O}(l) at 100∘C100^\circ\text{C} or 0∘C0^\circ\text{C} due to latent heat of vaporization.

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Thermochemical Equation of Methane Combustion

The balanced chemical equation including enthalpy describing the burning of methane: CH4(g)+2O2(g)→CO2(g)+2H2O(g)\text{CH}_4(g) + 2\text{O}_2(g) \rightarrow \text{CO}_2(g) + 2\text{H}_2\text{O}(g) with a molar heat of combustion of ΔcHm=−802.3 kJ/mol\Delta_c H_m = -802.3\,\text{kJ/mol}.

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Endothermic Heat of Decomposition (ΔdH\Delta_d H of HCl\text{HCl})

The positive enthalpy change of the decomposition reaction 2HCl(g)→H2(g)+Cl2(g)2\text{HCl}(g) \rightarrow \text{H}_2(g) + \text{Cl}_2(g) (ΔdH=+185.2 kJ\Delta_d H = +185.2\,\text{kJ}), indicating that the system must absorb heat at constant temperature, the product bonds are weaker than reactant bonds, and HCl(g)\text{HCl}(g) has a negative heat of formation.

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Ecological Perspective

A contextual viewpoint that evaluates processes based on environmental consequences, such as assessing the statement: "The use of fossil fuels as an industrial energy source contributes to global warming."