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Standard molar entropy

In chemistry, the standard molar entropy is the entropy content of one mole of pure substance at a standard state of pressure and any temperature of interest. These are often (but not necessarily) chosen to be the standard temperature and pressure.

The standard molar entropy at pressure = is usually given the symbol , and has units of joules per mole per kelvin (J⋅mol−1⋅K−1). Unlike standard enthalpies of formation, the value of is absolute. That is, an element in its standard state has a definite, nonzero value of S at room temperature. The entropy of a pure crystalline structure can be 0 J⋅mol−1⋅K−1 only at 0 K, according to the third law of thermodynamics. However, this assumes that the material forms a 'perfect crystal' without any residual entropy. This can be due to crystallographic defects, dislocations, and/or incomplete rotational quenching within the solid, as originally pointed out by Linus Pauling.[1] These contributions to the entropy are always present, because crystals always grow at a finite rate and at temperature. However, the residual entropy is often quite negligible and can be accounted for when it occurs using statistical mechanics.

Thermodynamics edit

If a mole of a solid substance is a perfectly ordered solid at 0 K, then if the solid is warmed by its surroundings to 298.15 K without melting, its absolute molar entropy would be the sum of a series of N stepwise and reversible entropy changes. The limit of this sum as   becomes an integral:

 

In this example,   and   is the molar heat capacity at a constant pressure of the substance in the reversible process k. The molar heat capacity is not constant during the experiment because it changes depending on the (increasing) temperature of the substance. Therefore, a table of values for   is required to find the total molar entropy. The quantity   represents the ratio of a very small exchange of heat energy to the temperature T. The total molar entropy is the sum of many small changes in molar entropy, where each small change can be considered a reversible process.

Chemistry edit

The standard molar entropy of a gas at STP includes contributions from:[2]

Changes in entropy are associated with phase transitions and chemical reactions. Chemical equations make use of the standard molar entropy of reactants and products to find the standard entropy of reaction:[3]

 

The standard entropy of reaction helps determine whether the reaction will take place spontaneously. According to the second law of thermodynamics, a spontaneous reaction always results in an increase in total entropy of the system and its surroundings:

 

Molar entropy is not the same for all gases. Under identical conditions, it is greater for a heavier gas.

See also edit

References edit

  1. ^ Pauling, Linus (1960). The Nature of the Chemical Bond (3rd ed.). Ithica, NY: Cornell University Press.
  2. ^ Kosanke, K. (2004). "Chemical Thermodynamics". Pyrotechnic chemistry. Journal of Pyrotechnics. p. 29. ISBN 1-889526-15-0.
  3. ^ Chang, Raymond; Cruickshank, Brandon (2005). "Entropy, Free Energy and Equilibrium". Chemistry. McGraw-Hill Higher Education. p. 765. ISBN 0-07-251264-4.

External links edit

standard, molar, entropy, chemistry, standard, molar, entropy, entropy, content, mole, pure, substance, standard, state, pressure, temperature, interest, these, often, necessarily, chosen, standard, temperature, pressure, standard, molar, entropy, pressure, di. In chemistry the standard molar entropy is the entropy content of one mole of pure substance at a standard state of pressure and any temperature of interest These are often but not necessarily chosen to be the standard temperature and pressure The standard molar entropy at pressure P 0 displaystyle P 0 is usually given the symbol S and has units of joules per mole per kelvin J mol 1 K 1 Unlike standard enthalpies of formation the value of S is absolute That is an element in its standard state has a definite nonzero value of S at room temperature The entropy of a pure crystalline structure can be 0 J mol 1 K 1 only at 0 K according to the third law of thermodynamics However this assumes that the material forms a perfect crystal without any residual entropy This can be due to crystallographic defects dislocations and or incomplete rotational quenching within the solid as originally pointed out by Linus Pauling 1 These contributions to the entropy are always present because crystals always grow at a finite rate and at temperature However the residual entropy is often quite negligible and can be accounted for when it occurs using statistical mechanics Contents 1 Thermodynamics 2 Chemistry 3 See also 4 References 5 External linksThermodynamics editIf a mole of a solid substance is a perfectly ordered solid at 0 K then if the solid is warmed by its surroundings to 298 15 K without melting its absolute molar entropy would be the sum of a series of N stepwise and reversible entropy changes The limit of this sum as N displaystyle N rightarrow infty nbsp becomes an integral S k 1 N D S k k 1 N d Q k T 0 T 2 d S d T d T 0 T 2 C p k T d T displaystyle S circ sum k 1 N Delta S k sum k 1 N frac dQ k T rightarrow int 0 T 2 frac dS dT dT int 0 T 2 frac C p k T dT nbsp In this example T 2 298 15 K displaystyle T 2 298 15K nbsp and C p k displaystyle C p k nbsp is the molar heat capacity at a constant pressure of the substance in the reversible process k The molar heat capacity is not constant during the experiment because it changes depending on the increasing temperature of the substance Therefore a table of values for C p k T displaystyle frac C p k T nbsp is required to find the total molar entropy The quantity d Q k T displaystyle frac dQ k T nbsp represents the ratio of a very small exchange of heat energy to the temperature T The total molar entropy is the sum of many small changes in molar entropy where each small change can be considered a reversible process Chemistry editThe standard molar entropy of a gas at STP includes contributions from 2 The heat capacity of one mole of the solid from 0 K to the melting point including heat absorbed in any changes between different crystal structures The latent heat of fusion of the solid The heat capacity of the liquid from the melting point to the boiling point The latent heat of vaporization of the liquid The heat capacity of the gas from the boiling point to room temperature Changes in entropy are associated with phase transitions and chemical reactions Chemical equations make use of the standard molar entropy of reactants and products to find the standard entropy of reaction 3 D S r x n S p r o d u c t s S r e a c t a n t s displaystyle Delta S circ rxn S products circ S reactants circ nbsp The standard entropy of reaction helps determine whether the reaction will take place spontaneously According to the second law of thermodynamics a spontaneous reaction always results in an increase in total entropy of the system and its surroundings D S t o t a l D S s y s t e m D S s u r r o u n d i n g s gt 0 displaystyle Delta S total Delta S system Delta S surroundings gt 0 nbsp Molar entropy is not the same for all gases Under identical conditions it is greater for a heavier gas See also editEntropy Heat Gibbs free energy Helmholtz free energy Standard state Third law of thermodynamicsReferences edit Pauling Linus 1960 The Nature of the Chemical Bond 3rd ed Ithica NY Cornell University Press Kosanke K 2004 Chemical Thermodynamics Pyrotechnic chemistry Journal of Pyrotechnics p 29 ISBN 1 889526 15 0 Chang Raymond Cruickshank Brandon 2005 Entropy Free Energy and Equilibrium Chemistry McGraw Hill Higher Education p 765 ISBN 0 07 251264 4 External links editStandard Thermodynamic Properties of Chemical Substances Table permanent dead link Retrieved from https en wikipedia org w index php title Standard molar entropy amp oldid 1174557019, wikipedia, wiki, book, books, library,

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