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Enthalpy
represented as H
energy change
quantifies as the heat flow into or out of the system in a process that occurs at constant pressure
tells us about the “heat content of a system”
state function (path independent)
depends only on reactants and products
Enthalpy of Reactions
represented as ∆Hrxn
heat transferred in a chemical reaction held at constant pressure
the difference between the enthalpies of the products and enthalpies of the reactants
∆H = H(products) - H(reactants)
Enthalpy of Endothermic Processes
H(products) > H (reactants)
∆H is positive
Enthalpy of Exothermic Processes
H(products) < H (reactants)
∆H is negative
Thermochemical Equations
equations that show the mass relationships between the substances involved in a reaction, alongside its corresponding enthalpy change
Rules in Interpreting Thermochemical Equations
Specify the physical states of all reactants and products as they can influence the resulting enthalpy
Reversing a reaction entails that the sign of ∆H reverses as well
If you multiply both sides of the equation by a factor of n, then multiply ∆H by the same factor of n.
The stochiometric coefficients, which are the numbers beside each reactant and product, refer to the number of moles of a substance.
Standard Enthalpy (∆Hºrxn or ∆Hºf)
enthalpy of a reaction carried out at 1 atm, as substances are said to be at the standard state at this point
∆Hºf of any element in its standard state is therefore 0
Formulas for Standard Enthalpy of Reaction (Summation)
∆Hºrxn = ∑(n∆Hºf products) - ∑(n∆Hºf reactants)
or
In formula [aA + bB → cC + dD]
where a, b, c, d = stoichiometric coefficients and A, B, C, D = reactants/products
∆Hºrxn = [c∆Hºf (C) + d∆Hºf (D)] - [a∆Hºf (A) + b∆Hºf (B)]
Hess’ Law
The overall enthalpy change in converting reactants to products is the same, regardless if the reaction took place in one step or in a series of steps
The sum of the ∆Hºrxn of the sub-processes is the sum of the overall reaction
Calculating ∆Hºrxn with Hess’ Law
Balance the chemical reaction
Manipulate the sub-step processes to ensure that the products and reactants are the same with the 1-step process. Reverse the sub-step processes if necessary,
Maipulate the coefficients to ensure it is the same with the 1-step process.
Cancel the substances found in both reactants and products.
Cancel the substances in both reactants and products.
Add the ∆Hºrxn of the sub-step processes to get ∆Hºrxn of the 1-step process.