Standard states:
A pressure of 1 atm and a constant temperature (25˚C) are taken as
standard states.
State
|
Standard states
|
Gas
|
Ideal gas at the given temperature and 1 atm
|
Liquid
|
Pure liquid at the given temperature and 1
atm
|
Solid
|
Stable crystalline from at given temperature
and 1 atm pressure
|
Heat of reaction:
Heat of reaction is defined as the amount of heat evolved or
absorbed when the reacting species, as represented by a balanced chemical
equation, have completely reacted. Enthalpy or heat of reaction is given
by
∆Hr = (sum of enthalpies of products) – (sum of enthalpies of
reactants)
ΔH = ∑aiHf products − ∑biHf reactants
ai and bi = stoichiometric coefficients of
products and reactants
In the calculation of heat of reaction, it is a convention to
assume that the heat of formation of elements in their standard state is zero.
Factors
affecting heat of reaction:
Physical state of
reactants and products:
H2(g) + ½ O2(g) → H2O(g); ΔH = − 57.8 kcal
H2(g) + ½ O2(g) → H2O(l); ΔH = − 68.32 kcal
Allotropic forms
of the element:
C(diamond) + O2(g) → CO2(g); ΔH = − 94.3kcal
C(amorphous) + O2(g) → CO2(g); ΔH = − 97.6kcal
Temperature:
ΔHT₂ - ΔHT₁ / T₂ - T₁ = ΔCp
ΔUT₂ - ΔUT₁ / T₂ - T₁ = ΔCv
Enthalpies
of Phase Transition:
Enthalpy of fusion:
It is the enthalpy change involved in the conversion of one mole
of a substance from solid state to liquid state at its melting point.
This equals the latent heat of fusion per gram multiplied by the molar mass.
This equals the latent heat of fusion per gram multiplied by the molar mass.
For example:
H2O(s)
→ H2O(l); Δfus
Hθ = 1.44kcal/mol
Enthalpy of
vaporization:
It is the enthalpy change involved in converting one mole of the
substance from liquid state to gaseous state at its boiling point.
For example:
H2O(l) → H2O(g); ΔvapH = 10.5kcal/mol
Enthalpy of
sublimation:
It is the enthalpy change involved in the conversion of one mole
of a solid directly into its vapor at a given temperature below its melting
point.
ΔsubH = ΔfusH + ΔvapH
For example:
I2(s) → I2(g); ΔsubH = 14.9kcal/mol
Enthalpy or Heat
of Formation:
The amount of heat evolved or absorbed when one mole of a
substance is formed from its constituent elements is called the heat of
formation.
Standard enthalpy of formation.
Standard enthalpy of formation.
It is the enthalpy change of a reaction by which a compound is formed from its constituent elements, the reactants and products, at standard state (i.e., at 298K and 1 atm pressure). Its symbol is Δf H⊝.
By convention, standard enthalpy for formation, Δf H⊝ of an element in reference state, i.e., its most stable state of aggregation is
taken as zero.
C (s) + O2 (g) → CO2 (g); Δf H⊝ =
-393.51 kJ/mol
The compounds having positive enthalpies of formation are called endothermic compounds and are less stable than the reactants.
The compounds having negative enthalpies of formation are known as
exothermic compounds and are more stable than the reactants.
Thermochemical
equation:
A Thermochemical Equation is a balanced
stoichiometric chemical equation that includes
the enthalpy change, ΔH. In variable form, a thermochemical equation
would look like this:
A + B → C; ΔH = (±) x
Where {A, B, C} are the usual agents of a chemical equation with
coefficients and “(±) x” is a positive or negative numerical value, usually
with units of kJ.
Endothermic reaction: A + B + Heat → C, ΔH > 0
Exothermic reaction: A + B → C + Heat, ΔH < 0
Hess's
Law:
If a specified set of reactants is transformed to a specified set
of products by more than one sequence of reactions, the total enthalpy change
must be the same for every sequence.
The enthalpy change in a chemical or physical process is the same
whether the process is carried out in one step or in several steps.
Example:
Calculate the enthalpy of the following chemical reaction:
CS2(l) + 3O2(g) → CO2(g) +
2SO2(g)
Given:
C(s) + O2(g) → CO2(g); ΔH = -393.5 kJ/mol --- (i)
S(s) + O2(g) → SO2(g); ΔH = -296.8 kJ/mol --- (ii)
C(s) + 2S(s) → CS2(l); ΔH = +87.9 kJ/mol ---- (iii)
S(s) + O2(g) → SO2(g); ΔH = -296.8 kJ/mol --- (ii)
C(s) + 2S(s) → CS2(l); ΔH = +87.9 kJ/mol ---- (iii)
Solution:
Leave eq 1 untouched (want CO2 as a product)
multiply second eq by 2 (want to cancel 2S, also want 2SO2 on product side)
flip 3rd equation (want CS2 as a reactant)
multiply second eq by 2 (want to cancel 2S, also want 2SO2 on product side)
flip 3rd equation (want CS2 as a reactant)
2) The result:
C(s) + O2(g) → CO2(g); ΔH = -393.5 kJ/mol
2S(s) + 2O2(g) → 2SO2(g); ΔH = -593.6 kJ/mol ← ( multiply by 2 on the ΔH )
CS2(ℓ) → C(s) + 2S(s); ΔH = -87.9 kJ/mol ← ( sign change on the ΔH)
2S(s) + 2O2(g) → 2SO2(g); ΔH = -593.6 kJ/mol ← ( multiply by 2 on the ΔH )
CS2(ℓ) → C(s) + 2S(s); ΔH = -87.9 kJ/mol ← ( sign change on the ΔH)
3) Add the three revised equations. C and 2S will cancel.
CS2(l) + 3O2(g) → CO2(g) +
2SO2(g)
4) Add the three enthalpies for the final answer.
ΔH = -1075 kJ/mol
Some things to
remember:
If you have to reverse a reaction to get things to cancel, the
sign of ΔH must also be reversed.
If you have to multiply an agent to get it to cancel, all other
agents and ΔH must also be multiplied by that number.
Generally ΔH values given in tables are under 1atm and 25 °C
(298.15 K), so be aware of what conditions your reaction is under.
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