Thermochemistry
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Transcript of Thermochemistry
![Page 1: Thermochemistry](https://reader035.fdocuments.in/reader035/viewer/2022062517/568136ab550346895d9e50a6/html5/thumbnails/1.jpg)
ThermochemistryPart II : Enthalpy
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Review: Temperature A measure of the average kinetic energy of
the particles that make up a substance or system
Change in temp represents a change in kinetic energy
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Systems and surroundings: System: area where reaction takes place
(generally is the reaction) Surroundings: outside of the system
Closed verses open systems
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Open-system both matter and energy
can freely cross from the system to the surroundings and back.
Ex: an open test tube
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Closed-System energy can cross the
boundary, but matter cannot.
Ex: a sealed test tube
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Isolated-System neither matter nor
energy can cross between the system and the surroundings.
Ex: The universe there are no
surroundings to exchange matter or energy with (as far as we know!)
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Enthalpy (∆H) a.k.a heat of reaction Chemical rxn (and phase changes) involve
changes in potential energy not kinetic Enthalpy is the potential energy change of a
system during process like chem rxn (or phase change)
Units: kJ/mol
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Chemical Rxns: The internal energy of a reactant or product
cannot be measured, but their change in enthalpy can
Enthalpy changes represent the diff between PE of products and PE of reactants
PE changes result from bonds being broken and/or formed
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Breaking a bond requires energy!
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Creating a bond releases energy !
(Strength of bond determines the energy needed to break or create bond)
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Exothermic and Endothermic Rxns:
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Exo verses Endo: If energy is released out of the system then it is
considered to be an exothermic enthalpy change (exit).
If energy is absorbed into the system then it is considered to be an endothermic enthalpy change (enter).
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There are several different enthalpies that we will be looking at :
Enthalpy of Rxn (∆Hrxn) Standard enthalpy of Rxn (∆H0
rxn) -- at standard temp (25°C) and pressure (100 kPa)
Standard molar enthalpy of formation (∆H0f)
Standard molar enthalpy of combustion (∆H0
comb)
We use tables to find these VALUES!
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Standard enthalpy of Rxn (∆H0rxn)
Exothermic and endothermic 3 ways to represent:
Thermochemical equation (includes energy in eq) Chem eq + ∆H0
rxn beside Enthalpy diagrams
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Exothermic:
∆H0 is always negative!!!!!
Energy written on product side
1. H2 + ½ O2 H2O + 285.8 kJ
2. H2 + ½ O2 H2O ∆H0rxn= -285.8 kJ/mol
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Exothermic cont’d:
Hint: Arrow down for neg
and up for pos arrow goes toward the
products
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Endothermic:
∆H0 is always positive!!!!!
Energy written on reactant side
1. 117.3 kJ + MgCO3 MgO + CO2
2. MgCO3 MgO + CO2 ∆H0rxn= 117.3 kJ/mol
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Endothermic cont’d:
Hint: Arrow down for neg
and up for pos arrow goes toward the
products
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Compare:
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Enthalpy dependent on molar amounts: Linearly dependent (multiply by the stoich
coefficients)
Ex:
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Standard molar enthalpy of formation (∆H0f)
Is the quantity of energy that is absorbed (+) or released (-) when one mole of a compound is formed directly from its elements (so this is why you see ½ as coefficient)
Ex:
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Standard molar enthalpy of combustion (∆H0
comb)
Enthalpy associated with combustion of 1 mol of substance
Ex:
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HW Pg 643 # 15, 16, 17, 18