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Estimate the probability that a hydrogen atom at room temperature is in one of its first excited states (relative to the probability of being in the ground state). Don't forget to take degeneracy into account. Then repeat the calculation for a hydrogen atom in the atmosphere of the starγ UMa, whose surface temperature is approximately 9500 K.

Short Answer

Expert verified

As a result, no Hydrogen atoms can be found in the first excited state.

On this star, there is one atom in the first excited state out of 64500 hydrogen atoms.


Step by step solution

01

Given information

A hydrogen atom at room temperature is in one of its first excited states (relative to the probability of being in the ground state).

02

Explanation

With n = 2, assuming E1 is ground state energy and E2 is first excited state energy, the chance of finding the atom in either of the first excited states is:

Ps2=1Ze-E2/kT

The partition function is equal to the sum of the Boltzmann factors, but because the initial state has the greatest energy magnitude, we can approximate it as follows:

Z=∑se-E(s)/kT≈e-E1/kT

Substitute in the above equation

Ps2=eE1/kTe-E2/kTPs2=e-E2-E1/kT

There are four such states, therefore the probability of E2 equals Ps2multiplied by 4, so:

PE2=4e-E2-E1/kT

Substitute the energies and Boltzmann constant in eV (k = 8.617 x 10-5 eV/K) at room temperature T = 300 K for the energy of the ground state E1=-13.6 eV and the energy of the first excited state B2 =-3.4 eV.

PE2=4e-(-3.4eV-(-13.6eV))/8.617×10-5eV/K(300K)PE2=1.75×10-171

As a result, no Hydrogen atoms can be found in the first excited state.

03

Explanation

We must now calculate this probability for the star γUMa, which has a surface temperature of 9500 K, as follows:

PE2=4e-(-3.4eV-(-13.6eV))/8.617×10-5eV/K(9500K)PE2=1.55×10-5

On this star, there is one atom in the first excited state out of 64500 hydrogen atoms.

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Most popular questions from this chapter

In the numerical example in the text, I calculated only the ratio of the probabilities of a hydrogen atom being in two different states. At such a low temperature the absolute probability of being in a first excited state is essentially the same as the relative probability compared to the ground state. Proving this rigorously, however, is a bit problematic, because a hydrogen atom has infinitely many states.

(a) Estimate the partition function for a hydrogen atom at 5800 K, by adding the Boltzmann factors for all the states shown explicitly in Figure 6.2. (For simplicity you may wish to take the ground state energy to be zero, and shift the other energies according!y.)

(b) Show that if all bound states are included in the sum, then the partition function of a hydrogen atom is infinite, at any nonzero temperature. (See Appendix A for the full energy level structure of a hydrogen atom.)

(c) When a hydrogen atom is in energy level n, the approximate radius of the electron wavefunction is a0n2, where ao is the Bohr radius, about 5 x 10-11 m. Going back to equation 6.3, argue that the PdV term is Tot negligible for the very high-n states, and therefore that the result of part (a), not that of part (b), gives the physically relevant partition function for this problem. Discuss.

In the real world, most oscillators are not perfectly harmonic. For a quantum oscillator, this means that the spacing between energy levels is not exactly uniform. The vibrational levels of an H2 molecule, for example, are more accurately described by the approximate formula

En≈ϵ1.03n-0.03n2,n=0,1,2,…

where ϵ is the spacing between the two lowest levels. Thus, the levels get closer together with increasing energy. (This formula is reasonably accurate only up to about n = 15; for slightly higher n it would say that En decreases with increasing n. In fact, the molecule dissociates and there are no more discrete levels beyond n ≈15.) Use a computer to calculate the partition function, average energy, and heat capacity of a system with this set of energy levels. Include all levels through n = 15, but check to see how the results change when you include fewer levels Plot the heat capacity as a function of kT/ϵ. Compare to the case of a perfectly harmonic oscillator with evenly spaced levels, and also to the vibrational portion of the graph in Figure 1.13.

The analysis of this section applies also to liner polyatomic molecules, for which no rotation about the axis of symmetry is possible. An example is CO2, with ∈=0.000049eV. Estimate the rotational partition function for a CO2molecule at room temperature. (Note that the arrangement of the atoms isOCO, and the two oxygen atoms are identical.)

Suppose you have 10 atoms of weberium: 4 with energy 0 eV, 3 with energy 1 eV, 2 with energy 4 eV, and 1 with energy 6 eV.

(a) Compute the average energy of all your atoms, by adding up all their energies and dividing by 10.

(b) Compute the probability that one of your atoms chosen at random would have energy E, for each of the four values of E that occur.

(c) Compute the average energy again, using the formulaE¯=∑sE(s)P(s)

A particle near earth's surface traveling faster than about 11km/shas enough kinetic energy to completely escape from the earth, despite earth's gravitational pull. Molecules in the upper atmosphere that are moving faster than this will therefore escape if they do not suffer any collisions on the way out.

(a) The temperature of earth's upper atmosphere is actually quite high, around 1000K.Calculate the probability of a nitrogen molecule at this temperature moving faster than 11km/s, and comment on the result.

(b) Repeat the calculation for a hydrogen molecule (H2)and for a helium atom, and discuss the implications.

(c) Escape speed from the moon's surface is only about 2.4km/s. Explain why the moon has no atmosphere.

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