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Thermodynamics Chemistry Chapter 6

1. Thermodynamics chapter 6 discusses important terms like system, surroundings, open system, closed system, isolated system, homogeneous system, heterogeneous system, isothermal process, adiabatic process, isobaric process, isochoric process, and cyclic process. 2. It also discusses state functions like internal energy, work, enthalpy, extensive and intensive properties, heat capacity, standard enthalpy of formation, entropy, Gibbs free energy, and spontaneity. 3. The chapter describes processes like phase changes, combustion reactions, and how to use concepts like Hess's law, Born-Haber cycles, and Gibbs free energy to determine reaction spontaneity.

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91 views11 pages

Thermodynamics Chemistry Chapter 6

1. Thermodynamics chapter 6 discusses important terms like system, surroundings, open system, closed system, isolated system, homogeneous system, heterogeneous system, isothermal process, adiabatic process, isobaric process, isochoric process, and cyclic process. 2. It also discusses state functions like internal energy, work, enthalpy, extensive and intensive properties, heat capacity, standard enthalpy of formation, entropy, Gibbs free energy, and spontaneity. 3. The chapter describes processes like phase changes, combustion reactions, and how to use concepts like Hess's law, Born-Haber cycles, and Gibbs free energy to determine reaction spontaneity.

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ajinkyarsingh2006
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© © All Rights Reserved
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Thermodynamics Chemistry Chapter 6

• Important Terms and Definitions


System: Refers to the portion of universe which is under observation.
Surroundings: Everything else in the universe except system is called surroundings. The
Universe = The System + The Surroundings.

Open System: In a system, when there is exchange of energy and matter taking place with
the surroundings, then it is called an open system.
For Example: Presence of reactants in an open beaker is an example of an open system.
Closed System: A system is said to be a closed system when there is no exchange of matter ‘
but exchange of energy is possible.
For example: The presence of reactants in a closed vessel made of conducting material.
Isolated System: In a system, when no exchange of energy or matter takes place with the
surroundings, is called isolated system.
For example: The presence of reactants in a thermoflask, or substance in an insulated closed
vessel is an example of isolated system.

Homogeneous System: A system is said to be homogeneous when all the constituents


present is in the same phase and is uniform throughout the system.
For example: A- mixture of two miscible liquids.
Heterogeneous system: A mixture is said to be heterogeneous when it consists of two or
more phases and the composition is not uniform.
For example: A mixture of insoluble solid in water. ’
The state of the system: The state of a thermodynamic system means its macroscopic or bulk
properties which can be described by state variables:
Pressure (P), volume (V), temperature (T) and amount (n) etc.
They are also known as state functions.
Isothermal process: When the operation is carried out at constant temperature, the process is
said to be isothermal. For isothermal process, dT = 0 Where dT is the change in temperature.
Adiabatic process: It is a process in which no transfer of heat between system and
surroundings, takes place.
Isobaric process: When the process is carried out at constant pressure, it is said to be
isobaric. i.e. dP = 0
Isochoric process: A process when carried out at constant volume, it is known as isochoric
in nature.
Cyclic process: If a system undergoes a series of changes and finally returns to its initial
state, it is said to be cyclic process.
Reversible Process: When in a process, a change is brought in such a way that the process
could, at any moment, be reversed by an infinitesimal change. The change r is called
reversible.
• Internal Energy
It is the sum of all the forms of energies that a system can possess.
In thermodynamics, it is denoted by AM which may change, when
— Heat passes into or out of the system
— Work is done on or by the system
— Matter enters or leaves the system.
Change in Internal Energy by Doing Work
Let us bring the change in the internal energy by doing work.
Let the initial state of the system is state A and Temp. TA Internal energy = uA
On doing’some mechanical work the new state is called state B and the temp. T B. It is found
to be
TB > TA
uB is the internal energy after change.
∴ Δu = uB – uA
Change in Internal Energy by Transfer of Heat
Internal energy of a system can be changed by the transfer of heat from the surroundings to
the system without doing work.
Δu = q
Where q is the heat absorbed by the system. It can be measured in terms of temperature
difference.
q is +ve when heat is transferred from the surroundings to the system. q is -ve when heat is
transferred from system to surroundings.
When change of state is done both by doing work and transfer of heat.
Δu = q + w
First law of thermodynamics (Law of Conservation of Energy). It states that, energy can
neither be created nor be destroyed. The energy of an isolated system is constant.
Δu = q + w.
• Work (Pressure-volume Work)
Let us consider a cylinder which contains one mole of an ideal gas in which a frictionless
piston is fitted.
• Work Done in Isothermal and Reversible Expansion of Ideal Gas

• Isothermal and Free Expansion of an Ideal Gas


For isothermal expansion of an ideal gas into vacuum W = 0
• Enthalpy (H)
It is defined as total heat content of the system. It is equal to the sum of internal energy and
pressure-volume work.
Mathematically, H = U + PV
Change in enthalpy: Change in enthalpy is the heat absorbed or evolved by the system at
constant pressure.
ΔH = qp
For exothermic reaction (System loses energy to Surroundings),
ΔH and qp both are -Ve.
For endothermic reaction (System absorbs energy from the Surroundings).
ΔH and qp both are +Ve.
Relation between ΔH and Δu.

• Extensive property
An extensive property is a property whose value depends on the quantity or size of matter
present in the system.
For example: Mass, volume, enthalpy etc. are known as extensive property.
• Intensive property
Intensive properties do not depend upon the size of the matter or quantity of the matter
present in the system.
For example: temperature, density, pressure etc. are called intensive properties.
• Heat capacity
The increase in temperature is proportional to the heat transferred.
q = coeff. x ΔT
q = CΔT
Where, coefficient C is called the heat capacity.
C is directly proportional to the amount of substance.
Cm = C/n
It is the heat capacity for 1 mole of the substance.
• Molar heat capacity
It is defined as the quantity of heat required to raise the temperature of a substance by 1°
(kelvin or Celsius).
• Specific Heat Capacity
It is defined as the heat required to raise the temperature of one unit mass of a substance by
1° (kelvin or Celsius).
q = C x m x ΔT
where m = mass of the substance
ΔT = rise in temperature.
• Relation Between Cp and Cv for an Ideal Gas
At constant volume heat capacity = Cv
At constant pressure heat capacity = Cp
At constant volume qv= CvΔT = ΔU
At constant pressure qp = Cp ΔT = ΔH
For one mole of an ideal gas
ΔH = ΔU + Δ (PV) = ΔU + Δ (RT)
ΔH = ΔU + RΔT
On substituting the values of ΔH and Δu, the equation is modified as
Cp ΔT = CvΔT + RΔT
or Cp-Cv = R
• Measurement of ΔU and ΔH—Calorimetry
Determination of ΔU: ΔU is measured in a special type of calorimeter, called bomb
calorimeter.
Working with calorimeter. The calorimeter consists of a strong vessel called (bomb) which
can withstand very high pressure. It is surrounded by a water bath to ensure that no heat is
lost to the surroundings.
Procedure: A known mass of the combustible substance is burnt in the pressure of pure
dioxygen in the steel bomb. Heat evolved during the reaction is transferred to the water and
its temperature is monitored.
• Enthalpy Changes During Phase Transformation
Enthalpy of fusion: Enthalpy of fusion is the heat energy or change in enthalpy when one
mole of a solid at its melting point is converted into liquid state.

Enthalpy of vaporisation: It is defined as the heat energy or change in enthalpy when one
mole of a liquid at its boiling point changes to gaseous state.
Enthalpy of Sublimation: Enthalpy of sublimation is defined as the change in heat energy or
change in enthalpy when one mole of solid directly changes into gaseous state at a
temperature below its melting point.

• Standard Enthalpy of Formation


Enthalpy of formation is defined as the change in enthalpy in the formation of 1 mole of a
substance from its constituting elements under standard conditions of temperature at 298K
and 1 atm pressure.

Enthalpy of Combustion: It is defined as the heat energy or change in enthalpy that


accompanies the combustion of 1 mole of a substance in excess of air or oxygen.
• Thermochemical Equation
A balanced chemical equation together with the value of ΔrH and the physical state of
reactants and products is known as thermochemical equation.

Conventions regarding thermochemical equations


1. The coefficients in a balanced thermochemical equation refer to the number of moles of
reactants and products involved in the reaction.

• Hess’s Law of Constant Heat Summation


The total amount of heat evolved or absorbed in a reaction is same whether the reaction takes
place in one step or in number of steps.
• Born-Haber Cycle
It is not possible to determine the Lattice enthalpy of ionic compound by direct experiment.
Thus, it can be calculated by following steps. The diagrams which show these steps is known
as Born-Haber Cycle.

• Spontaneity
Spontaneous Process: A process which can take place by itself or has a tendency to take
place is called spontaneous process.
Spontaneous process need not be instantaneous. Its actual speed can vary from very slow to
quite fast.
A few examples of spontaneous process are:
(i) Common salt dissolves in water of its own.
(ii) Carbon monoxide is oxidised to carbon dioxide of its own.
• Entropy (S)
The entropy is a measure of degree of randomness or disorder of a system. Entropy of a
substance is minimum in solid state while it is maximum in gaseous state.
The change in entropy in a spontaneous process is expressed as ΔS
• Gibbs Energy and Spontaneity
A new thermodynamic function, the Gibbs energy or Gibbs function G, can be defined as G =
H-TS
ΔG = ΔH – TΔS
Gibbs energy change = enthalpy change – temperature x entropy change ΔG gives a criteria
for spontaneity at constant pressure and temperature, (i) If ΔG is negative (< 0) the process is
spontaneous.
(ii) If ΔG is positive (> 0) the process is non-spontaneous.
• Free Energy Change in Reversible Reaction

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