CALORIMETRY

calorimeter – device used to measure the amount of

heat absorbed or released during a

chemical or physical process

Law of Conservation of Energy – in any physical or chemical

process energy is neither created nor destroyed, it is conserved

(all energy is work, heat, or stored energy)

heat lost = heat gained or q (lost) = – q (gained)

(m lost x C lost x T lost) = – (m gained x C gained x Tgained)

Ex 1: If 10 g of aluminum at 109oC is added to 50 g water at 24.0oC, the

temperature of the final mix is 27.5oC. What is the specific heat of Al?

aluminum water

m Al =10 g m H2O = 50 g

TAl = Tf – Ti = – 81.5oC TH2O= Tf – Ti= 3.5oC

CAl = ? CH2O = 1cal/goC

heat lost by Al = heatgained by H2O: q Al = –q H2O

(mAl x CAl x TAl) = – (mH2O x C H2Ox TH2O)

(10 g) (CAl) (– 81.5oC) = – (50 g) (1 cal/goC) (3.5oC)

(– 815 g oC) (C Al) = – 175 cal so C Al= .215 cal/goC

Ex 2: If 250 g of silver at 50.0oC is added to 125 g of water at 23.0oC

What is the final temperature of the mixture? (C Ag = 0.0566 cal/goC)

Ag: m Ag = 250 g H2O: m H2O =125 g

Ti Ag = 50.0oC Ti H2O = 23.0oC

CAg = 0.0566 cal/goC CH2O = 1 cal/goC

qAg = - qH2O or mAg x CAg x TAg = – (mH2O x CH2O x TH2O )

250 g x 0.0566 cal/goC x (Tf – 50oC) = – 125 g x 1cal/goC x (Tf – 23oC)

(14.15 cal/oC) Tf - 707.5 cal = -125 cal/oC) Tf + 2875 cal

- 3582.5 cal = -139.15 cal x Tf

- 3582.5 cal/-139.15 cal = Tf = 25.75oC

THERMOCHEMISTRY

enthalpy – heat content of a system measured at

constant pressure

enthalpy change – quantity of heat gained or lost

during a process at constant pressure

Heat of Reaction ( H) the heat absorbed or released

during a chemical reaction

H = Hproducts - Hreactants

exothermic reaction – releases energy in the form of heat; H is negative

heat appears on the products side of the equation

 H reactants > H products

endothermic reaction – absorbs or requires energy in

the form of heat; H is positive

heat appears on the reactants side of the equation

 H products > H reactants

thermochemical equation - a chemical equation that shows

the amount of heat produced orabsorbed by a reaction

2 H2 (g) + O2 (g)  2 H2O (g) H = - 483.6 kJ (bonds forming = exo.)

2 H2O (g)  2 H2 (g) + O2 (g) H = + 483.6 kJ(bonds breaking = endo.)

molar heat of formation ( Hof) quantity of heat absorbed

or released when one mole of a compound is formed from its elements at standard state

(1 atm & 25oC)

Based on 1 mole of products:

H2 (g) + ½ O2 kJ/mol (g)  H2O (l)Hof = - 285.8 kJ

High “-” Hof implies a substance is more stable

than its elements

High “+” Hof implies a substance is less stable

than its elements

heat of combustion – quantity of heat released by the

complete combustion of 1 mole of a substance

Calculating Heats of Reaction

Enthalpy changes can be calculated in 2 ways:

A. Using standard heats of formation :

Ho = Hof (products ) - Hof (reactants)

Ex 1: Use the heats of formation to find the enthalpy change for the

combustion of methane gas (CH4) to form carbon dioxide gas

and liquid water.

  1. Write balanced equation:

CH4 (g) + 2 O2 (g)  CO2 (g) + 2 H2O (l)

  1. Look up standard heats of formation:

CH4 (g) = - 74.81 kJ O2 (g) = 0 kJ

CO2 (g) = - 393.51 kJ H2O (l) = -285.83 kJ

3. Sum the Hof of the reactants and the products taking into

account the number of moles of each:

Ho = Hof (products ) - Hof (reactants)

= - 393.51 kJ + (2 mol) (- 285.83 kJ) – (- 74.81 kJ)

= - 393.51 kJ – 571.66 kJ + 74.81 kJ

= - 890.36 kJ H is negative so rxn is exoth.

Practice: Calculate the heat of reaction (enthalpy change) for the

combustion of 2 moles of sulfur dioxide gas into 2 moles of

sulfur trioxide gas.

  1. Write balanced equation: 2SO2 (g) + O2 (g)  2SO3 (g)
  1. Look up standard heats of formation:

SO3 (g) = - 395.72 kJ SO2 (g) = - 296.83 kJ

3. Sum the Hof of the reactants and the products

Ho = Hof (products ) - Hof (reactants)

= (2 mol) (- 395.72 kJ) – (2 mol) (- 296.83 kJ)

= - 791.44 kJ + 593.66 kJ

= -197.78 kJ exothermic reaction

B. Using Hess’s Law of Heat Summation and a given set of equations:

Hess’s Law – the overall enthalpy change for a reaction is

equal to the sum of the enthalpychanges for

the individual steps in the process

Ex 2: What is the heat of reaction for the decomposition of solid ice to its

elements?

target equation: H2O (s)  H2 (g) + ½ O2 (g)H = ? kJ

H2 (g) + ½ O2 (g)  H2O (l)Hof = - 285.8 kJ

H2O (s)  H2O (l)Hof = 6.0 kJ

Solution: H2O (s)  H2O (l)Hof = 6.0 kJ

H2O (l)  H2 (g) + ½ O2 (g)Hof = + 285.8 kJ

H2O (s)  H2 (g) + ½ O2 (g) H = + 291.8 kJ

Rules for manipulating thermochemical equations:

1. When an equation is reversed, the Hof must also be reversed.

2. Formulas cancelled from both sides of the equation must be the

same substance in the same physical state.

3. If all the coefficients of an equation are multiplied or divided by

the same factor, Hof must also be changed by the same factor.

Practice: What is the enthalpy change for the formation silicon from

SiCl4 and Mg? H = ? kJ

Target equation: 2Mg (s) + SiCl4 (l) Si (s) + 2 MgCl2 (s)

Si (s) + 2 Cl2 (g)  SiCl4 (l)Hof = - 687 kJ

Mg (s) + Cl2 (g)  MgCl2 (s)Hof = - 641 kJ

SiCl4 (l)  Si (s) + 2 Cl2 (g)Hof = + 687 kJ

2x Mg (s) + Cl2 (g)  MgCl2 (s) 2( Hof = - 641) = - 1282 kJ

2Mg (s) + SiCl4 (l) Si (s) + 2 MgCl2 (s) H = - 595 kJ