Ideal Gases vs. Real Gaseschem107.chem.tamu.edu/brown/slides/1023_2.pdf · Real Gases: Van der...

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CHEM 107, Fall 2019 © 2019, L.S. Brown 1 Ideal Gases vs. Real Gases Most gases obey the ideal gas law under normal conditions… but most substances are not gases under normal conditions Limitations on use of ideal gas model? check assumptions of model Assumptions in Ideal Gas Model Of various assumptions, the two most questionable are: The molecules themselves occupy zero volume (i.e., point masses) The molecules do not exert any attractive or repulsive forces upon each other When are these assumptions unreasonable? High pressures and/or low temperatures

Transcript of Ideal Gases vs. Real Gaseschem107.chem.tamu.edu/brown/slides/1023_2.pdf · Real Gases: Van der...

Page 1: Ideal Gases vs. Real Gaseschem107.chem.tamu.edu/brown/slides/1023_2.pdf · Real Gases: Van der Waals Equation •The aterm corrects for non-zero forces between molecules •The bterm

CHEM 107, Fall 2019

© 2019, L.S. Brown 1

Ideal Gases vs. Real Gases

• Most gases obey the ideal gas law under normal conditions…

• but most substances are not gases under normal conditions

• Limitations on use of ideal gas model?– check assumptions of model

Assumptions in Ideal Gas Model

• Of various assumptions, the two most questionable are:– The molecules themselves occupy zero volume (i.e., point

masses)– The molecules do not exert any attractive or repulsive

forces upon each other• When are these assumptions unreasonable?• High pressures and/or low temperatures

Page 2: Ideal Gases vs. Real Gaseschem107.chem.tamu.edu/brown/slides/1023_2.pdf · Real Gases: Van der Waals Equation •The aterm corrects for non-zero forces between molecules •The bterm

CHEM 107, Fall 2019

© 2019, L.S. Brown 2

Real Gases:Van der Waals Equation

•The a term corrects for non-zero forces between molecules•The b term corrects for molecular volume•Both a and b depend on identity of the gas!

𝑃 +𝑎𝑛%

𝑉%𝑉– 𝑛𝑏 = 𝑛𝑅𝑇

Still no need to memorize this equation!

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Gas a(atm L2 mol–2)

b(L mol-1)

He 0.034 0.0237H2 0.2444 0.02661Ar 1.345 0.03219N2 1.390 0.03913

CH4 2.253 0.04278H2O 5.464 0.03049HF 9.433 0.0739SF6 7.747 00879

van der Waals constants for some common gases

a accounts for intermolecular forces.

b accounts for excluded volume

Intermolecular Forces (IMFs)• Responsible for the existence of condensed phases

(solids & liquids)• Based on Coulomb forces• Much weaker than chemical bonds• Types to consider (all very similar, but strengths vary):

– dipole forces– dispersion forces– hydrogen bonding

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• In a collection of dipoles, oppositely charged ends of the dipoles will attract each other. Similarly charged ends will repel.

• These forces will cause dipoles to line up with one another and “stick together.”

Dipole Forces

+–+

+–+or

Polar Molecules

• Many molecules have a dipole moment due to polarity of bonds & shape of molecule

• These polar molecules will be influenced by dipolar forces.

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Dispersion Forces• Non-polar molecules also form condensed phases. H2

boils at20 K, and He boils at 4.2 K (at 1 atm pressure)• Forces?

→“Dispersion forces” due to induced dipoles• Arise because electron cloud is not static• Present in all molecules (and geckos…)

Transient Dipoles - H2 example

• H2 molecule: average e– density is symmetric• But at any given instant, the e– density may be bigger

on one “end” of the molecule than on the other, creating a transient dipole.

• The transient dipole in one molecule will influence other molecules, so that the induced dipoles will “line up” just like “real” or permanent dipoles.

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Transient Dipoles - H2 example

H2, one e– on each end H2, both e–’s on same end,producing temporary dipole

– +

– +

– +

Transient dipole sets up similar dipoles in nearby molecules,and molecules line up to maximize attractive forces.

Strength of Intermolecular Forces

• Strength of forces between molecules determines physical state (solid, liq., gas)

• Strength of dispersion forces increases as molecules become larger.– more e–’s ® more “polarizable”

• Stronger intermolecular forces lead to higher melting & boiling points.

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Intermolecular forces & physical state

F2: gas at 298 K

Br2: liquid at 298 K

Strength of Intermolecular Forces

• Big, heavy molecules tend to have high boiling points.• Polar molecules tend to have higher boiling points

than non-polar molecules with similar size & shape.

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Hydrogen Bonding

• Special case of dipole-dipole interaction• Stronger than usual due to small size of H-atom• Occurs only in molecules containing H bound to a very

electronegative atom (F, O, or N)• H “end” of one molecule is attracted to the

electronegative “end” of another molecule

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Hydrogen bonds and water

• H-bonds give water some special properties:– high melting & boiling points, essential for our existence– structure of ice is very “open” and very stable– density of water increases slightly on melting, so ice floats

• H-bonds also important in structure of bio-molecules like proteins, DNA, ...

Hydrogen Bonding in Ice

Open structure leads to low density, so ice floats in liquid water.

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141.5 pm

154 pm

335 pmbetween layers

Graphite Diamond

Vapor Pressure and Boiling Point• Strength of intermolecular

forces governs boiling (and melting) points.

• Vapor pressure is gas pressure above a liquid in a closed container.

• “Normal boiling point”: boiling point at P = 1 atm, or T at which vapor pressure = 1 atm

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Phase Diagrams• Graphical representation

of most stable phase (or phases) under different conditions.

• Shown here for water.• These get much more

complicated for alloys, andmany of you will see them again in a future course.

H2O CO2