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Energy Changes in Chemical Reactions Exothermic Reaction Is One That Releases Energy in The Form of Heat or

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Thermochemistry

Energy Changes in Chemical Reactions

Exothermic reaction is one that releases energy in the form of heat or


light. Another way of describing an exothermic reaction is that it is one in
which the energy of the products is less than the energy of the reactants,
because energy has been released during the reaction.

Endothermic reaction is one that absorbs energy in the form of heat or


light. It is one in which the energy of the products is greater than the
energy of the reactants, because energy has been absorbed during the
reaction.

First Law of Thermodynamics

The first law of thermodynamics is a version of the law of conservation


of energy, adapted for thermodynamic systems. The law of conservation
of energy states that the total energy of an isolated system is constant;
energy can be transformed from one form to another, but can be neither
created nor destroyed. The first law is often formulated:

ΔU=Q−W

It states that the change in the internal energy ΔU of a closed system is


equal to the amount of heat Q supplied to the system, minus the amount
of work W done by the system on its surroundings. An equivalent
statement is that perpetual motion machines of the first kind are
impossible.

Thermochemical Equations
Balanced chemical equations that show the enthalpy relation between
products and reactants

H2(g) + Cl2(g) → 2HCl(g); ∆H= -185 kJ

Exothermic reaction: 185 kJ of heat is evolved when 2moles of HCl are


formed.2HgO(s) → 2Hg(l) + O2(g); ∆H= +182 kJ

Endothermic reaction: 182 kJ of heat must be absorbed to decompose 2


moles HgO.

The sign of ∆H indicates whether the reaction isendothermic (+) or


exothermic (–)

• Coefficients in the equations represent thenumbers of moles of reactants


and products• Phases must be specified (s), (l), (g), (aq)

• The value quoted for ∆H applies when productsand reactants are at the
same temperature, usually25oC

Thermochemical Equations Rule #1

∆H is directly proportional to the amount of reactants and products.

When one mole of ice melts, ∆H = +6.00 kJ.

When one gram of ice melts, ∆H = +0.333 kJ.g-1

H2(g) + Cl2(g)→ 2HCl(g); ∆H = -185kJ1/2H2(g) + 1/2Cl2(g)→ HCl(g);


∆H = -92.5kJ

Thermochemical Equations Rule #2

∆H for a reaction is equal in magnitude but opposite in sign to ∆H for the


reverse reaction.

2HgO(s) → 2Hg(l) + O2(g); ∆H= +182 kJ2Hg(l) + O2(g) → 2HgO(s) ;


∆H= -182 kJ
Thermochemical Equations Rule #3

∆H is independent of the path of the reaction –it depends only on the


initial and final states

Thermochemical Equations Rule #3

∆H is independent of the path of the reaction –it depends only on the


initial and final states

Thermochemical Equations Rule #3

∆H is independent of the path of the reaction –it depends only on the


initial and final states

Standard enthalpy of formation and reaction Hess’ Law

Hess' Law is an early statement of the law of conservation of energy


(1840). It says that the heat liberated by a process doesn't depend on how
the process happens (only on the starting and ending states: in other
words, it's a state function). Now we know we should really use enthalpy
for this, not heat, because enthalpy is a state function, so this is true,
while heat is a process. Hess' Law lets us break a reaction or process into
a series of small, easily measured steps, and then we can add up the ΔH
of the steps to find the change in enthalpy of the whole thing. Hess' law is
a great way to think about chemical processes and make predictions.

Standard enthalpies of formation help us predict reaction enthalpies for


many reactions if the products and reactants are well-studied, even if the
specific reaction is new. To do this, we imagine that we take the reactants
and separate them into their pure elements in a standard state. The
standard state is the element in its most stable form at room temperature
and atmospheric pressure. Then we take the elements and recombine
them to make the products. The reaction enthalpy is equal to the
difference in the enthalpies of these processes.

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