How many possible arrangements are there for a deck of 52playing cards? (For simplicity, consider only the order of the cards, not whether they are turned upside-down, etc.) Suppose you start w e in the process? Express your answer both as a pure number (neglecting the factor of k) and in SI units. Is this entropy significant compared to the entropy associated with arranging thermal energy among the molecules in the cards?

Short Answer

Expert verified

The Boltzmann constant Swith and without.

  • With Boltzmann constant S=2.157 *10^21 J.K^1
  • With Boltzmann constant S = 156.36

Step by step solution

01

The entropy create in the process

  • In a standard pack of playing cards there are N=52different cards, so they can be arranged in:

Ω=N!=52!=8.07×1067ways

  • The size of this number is why it's highly unlikely that any card game that relies on dealing cards from a shuffled deck will ever repeat itself. The entropy of a shuffled deck is therefore:

S=klnΩ

substitute withk=1.38×1023JK1 S=1.38×10-23ln8.07×1067=2.157×10-21J·K-1

S=1.38×1023ln8.07×1067=2.157×1021JK1

02

Calculate without Boltzmann Constants

Without Boltzmann's constant we have,

S=lnΩ=ln(8.07x1067)=156.36

  • Although playing cards aren't made of an Einstein solid, the multiplicity of the macrostate in which thermal energy is exchanged among the cards will be something of similar order. The approximate multiplicity in the high temperature case for an Einstein solid with oscillators and q >> N energy quanta is

ΩqeNN

  • For Non the order of 1023 ,Ωis a very large number, so the thermal entropy of the cards is vastly greater than the entropy generated by shuffling the deck.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Fun with logarithms.
a Simplify the expressionealnb. (That is, write it in a way that doesn't involve logarithms.)
b Assuming that b<<a, prove that ln(a+b)(lna)+(b/a). (Hint: Factor out the afrom the argument of the logarithm, so that you can apply the approximation of part d of the previous problem.)

Use the Sackur-Tetrode equation to calculate the entropy of a mole of argon gas at room temperature and atmospheric pressure. Why is the entropy greater than that of a mole of helium under the same conditions?

Use a computer to reproduce the table and graph in Figure2.4: two Einstein solids, each containing three harmonic oscillators, with a total of six units of energy. Then modify the table and graph to show the case where one Einstein solid contains six harmonic oscillators and the other contains four harmonic oscillators (with the total number of energy units still equal to six). Assuming that all microstates are equally likely, what is the most probable macrostate, and what is its probability? What is the least probable macrostate, and what is its probability?

Use Stirling's approximation to find an approximate formula for the multiplicity of a two-state paramagnet. Simplify this formula in the limit NNto obtain ΩNe/NN. This result should look very similar to your answer to Problem 2.17; explain why these two systems, in the limits considered, are essentially the same.

Using the same method as in the text, calculate the entropy of mixing for a system of two monatomic ideal gases, Aand B, whose relative proportion is arbitrary. Let Nbe the total number of molecules and letx be the fraction of these that are of speciesB . You should find

ΔSmixing=Nk[xlnx+(1x)ln(1x)]

Check that this expression reduces to the one given in the text whenx=1/2 .

See all solutions

Recommended explanations on Physics Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free