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MCAT PREPARATION – SPRING 2019 How many things have to

Course: MCAT PREPARATION Delivered: Thursday, May 23, 2019 happen to you before
Instructor: Mr. Carlos Ortiz TBCB: Next Session something occurs to you?
Student: CARLOS ORTIZ/VIC POPP ETC: 60-90 Robert Frost

PP
Victoria, this PrePacket 2.2 continues with the information bulk properties of gases,
liquids, and solids. We will conclude with Fluidity & Rigidity, Diffusion, and Surface
Tension. We will then begin our study of INTERMOLECULAR FORCES, the strongest
of which will be the HYDROGEN BOND!
NOTA BENE (NB): While the HYDROGEN BOND may be the strongest of the

2.2
INTERMOLECULAR FORCES, it is still very weak when compared to
INTRAMOLECULAR COVALENT BONDS which require a decent amount of energy to
break. We’ll see that ENERGY is a guiding principle to our understanding of not only the
explicit BOND STRENGTHS that exist INSIDE and BETWEEN MOLECULES, but also to
our understanding of molecular behavior. READ ON, SCHOLAR!

# of Questions: 11
Topics: CHEMISTRY
Time: Will vary: Anywhere from 60-90 minutes
TBCB: NEXT SESSION
Notes/Instructions: CHEMISTRY: Bulk Properties of Gases,
Check these off as we Liquids, and Solids: A Molecular Interpretation
complete them. for the MCAT

PrePacket 2.2

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rigidity elasticity fluidity VISCOSITY volumes


STRONG rigid force viscous SHEAR

CHEMISTRY: Bulk Properties 5) The properties of hardness (that’s a


resistance to INDENTATION) and
MACROSCOPIC MEASUREMENT: Fluidity & elasticity (that’s the capacity to
Rigidity “rebound” or return to shape when a
As much as we’ve learned so far about deforming stress is removed) are very
condensed phases (solids and liquids) and closely related to rigidity and they all
gases, we still have not touched upon the indicate that solids have a HIGH SHEAR
MOST CHARACTERISTIC PROPERTY of gases VISCOSITY whereas liquids and solids
and liquids: their ability to FLOW, also known DO NOT.
Note: Av
1 1 =Av
as their fluidity. 2 2

6) The study of the flow or “fluidity” of


In stark contrast is the rigidity of solids matter, typically in a liquid state, is
which prevents them from flowing at all (and called rheology. The substances usually
also makes it difficult to deform or distort have a complex microstructure and
them). Let’s review some fundamentals: include muds, suspensions, certain
1) Liquids possess definite volumes but polymers, and even bodily fluids.
keep NO DEFINITE SHAPE! They actually
take on the SHAPES of whatever 1 SICKLED CELLS
containers they are in. a Abnormal rheologic behavior of sickle cells is the
result of increased viscosity of the blood caused by
2) Liquids flow easily under a stress (an polymerization of hemoglobin S and the resultant
externally applied force). production of dense, dehydrated sickle erythrocytes.
As the viscosity of the sickle cells increases there is
3) Liquids are viscous which is to say they a negative impact on blood flow which contributes to
possess an inherent RESISTANCE TO vascular occlusion and hypertension. It follows that
FLOW. On a microscopic level, we call it blood flow is
shear viscosity and it arises from a thin
A. inversely proportional to blood pressure and
layer of molecules being “dragged directly proportional to viscosity.
across” another layer – for some liquids,
this “drag” is very “sticky” while for ` B. directly proportional to blood pressure and
inversely proportional to viscosity.
others it is almost not “sticky” at all – in
other words, some liquids have great C. directly proportional to both blood pressure and
resistance to flow and therefore HIGH viscosity.
VISCOSITY while others have very little D. inversely proportional to both blood pressure
resistance to flow and are said to have and viscosity.
very LITTLE VISCOSITY. E. independent of blood pressure and viscosity.
Regardless of the level of shear Blood flows FASTER when BP his high, SLOWER when
BP is low (so directly proportional to BP). The opposite
viscosity, liquids still FLOW MUCH MORE is true for blood flow and VISCOSITY – so inversely
EASILY than any solid. In fact, the shear True orproportional
False to viscosity.
viscosities of most liquids are about 16 F The stronger the INTERMOLECULAR ATTRACTIVE
times LESS than those of most solids FORCES between molecules of a fluid, the less
(you can imagine that for GASES they viscous it is.
are even LESS). F It is more difficult for the human heart to pump low
viscosity blood than high viscosity blood.
4) A rigid material retains its SHAPE under T Blood viscosity is affected by red blood cell shape.
an applied stress; it is considered
F Solids and gases possess definite volumes.
structurally STRONG if it can RESIST
FLOW when stressed.
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tripled diffuse gases slower temperature

MACROSCOPIC MEASUREMENT: Diffusion


Victoria, the concept of diffusion should be
familiar to you. Ever walk by a perfume
counter in Macy’s (or elsewhere)? You get
“hit” almost immediately by the different
scents of all the perfumes that have been
sprayed and tested (and pushed and
promoted – those people are like DRUG
DEALERS!)
When two different substances are placed in
contact (consider a drop of food coloring in a
beaker of plain distilled water), they start to
mix – we say that molecules of one type,
THE FOOD COLORING MOLECULE, migrate or
diffuse into regions that were initially
occupied only by the other type, THE WATER
MOLECULE. 2 Diffusion across a cell membrane
CONSIDER GASES: Molecules dispersed in a According to the table above, assuming diffusion
GASES at room temperature diffuse at rates depended on nothing else other than the diffusing
on the order of centimeters per second species, the host species, and the temperature of
the diffusion environment, which of the following
(makes sense why we smell perfumes pretty would diffuse the most through 1 square meter of
quickly when walking by the counter). membrane?
Assume both sides of the membrane have BOTH the host
CONSIDER LIQUIDS & SOLIDS: Our food and diffusing species and that the membrane is FULLY
coloring example highlights the fact that permeable to that species.
diffusion rates in liquids and solids are far
slower. The diffusion constant of a A. CH4 at 273 K
substance measures the rate of diffusive Methane at 273 K has the highest
` B. Ar at 300 K
mixing. diffusion constant at 2.06 x 10-5
square meters per second.
C. O2 at 100 K
At room temperature and pressure,
diffusion constants for the diffusion of D. Ar at 100 K
liquids into liquids are about four
E. HCl at 200 K
orders of magnitude smaller than those
for gases into gases;
3 Diffusion Constant
Diffusion constants of solids into solids
a Which of the following is a possible diffusion
are MANY, MANY orders of magnitude
constant for F2 into F2 at 273 K?
smaller yet. Diffusion in solids is really
quite slow. Values of the diffusion 2
A. about 1.6 x 10-4 m per second
constant for selected materials are According to the table, the heavier
shown in the TABLE that follows in the ` B. about 1.8 x 10-5 m 2
per second
DIATOMIC gas will have the
smaller diffusion constant at the
next column on this page. Notice that the C. about 1.6 x 10-5 m 2
samepertemperature.
second The only choice
diffusion constant is measured in m2 that is smaller than the 1.8 x 10-5
D. about 1.8 x 10-4 m2 per second
per s and is apparently temperature diffusion constant of oxygen at 273
dependent as the rate for diffusion of Ar E. about 2.0 x 10-5 K
mis2 choice C.
per second
into Ar increased by almost 9 times when
the temperature was tripled.

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arrangement boundaries stress intermediate resists vibrate viscosity
spherical intermolecular tension water temperature freedom rigidity

MACROSCOPIC MEASUREMENT: Diffusion MACROSCOPIC MEASUREMENT: Surface Tension


Here’s another take on diffusion. Surface tension and its NATURAL
EXISTENCE is somewhat of a surprise to the
In liquids, molecules are free to travel
student of chemistry (and biology and
through the sample, changing neighbors
physics). Consider this:
constantly in the course of their diffusive
motion. This “freedom of movement” Phases (gases, liquids, solids) often co-
suggests that a liquid has low shear exist. The boundaries between these
viscosity, so its molecules can quickly phases is of special importance in
“change neighbors” as the liquid FLOWS in chemistry and biology. Each boundary
response to an external stress. has its own UNIQUE characteristics.
In solids, the molecules do not freely Let’s focus on the surface of water (or
move as they do in liquids, but they do any liquid for that matter) IN CONTACT
constantly vibrate about their equilibrium with air (or any gas). It turns out that
positions – they remain quite close to each the SURFACE OF THE LIQUID resists
other. This rigidity of the solid suggests, in attempts to increase its area (it just does
contrast to liquids, that a durable network NOT want to increase).
or arrangement of neighbors about any
given molecule exists most of the time. Check out this picture of a water droplet
DROPPING into water:
This durable arrangement of molecules
in a solid, as opposed to the FREEDOM OF
MOLECULES to diffuse more readily in a
liquid, is the critical difference between the
solid and liquid states. In the end, as far as
STRUCTURE goes, a liquid is essentially
intermediate between a gas and a solid.
4 Dissolution
a Considering diffusion of molecules, which of the
following is the most likely reason liquids can
dissolve substances more rapidly than do solids?
Surface tension works as follows in the
A. Individual molecules of a liquid move more picture above: The spherical shape of the
freely, making quicker contact with molecules of
water droplets is caused by surface tension.
an added substance; new attractions between
unlike molecules result in greater dissolution In the picture, a drop of water LANDED,
BOUNCED UP, and PULLED UP A COLUMN OF
` B. Liquid molecules have a greater hydrogen- WATER – all droplets, from the ONE THAT
bonding capacity to split molecules of an added
substance.
INITIALLY DROPPED to the ones that were
pulled up in the column of water are spherical
C. Liquids have a higher shear viscosity than solids
which allows them to dissolve molecules of an
because of surface tension.
added substance
While hydrogen bonding is areadily.
major factor in the We will soon understand more intimately that
dissolution of molecules that can hydrogen bond with
the D. Solids
solvent canmolecules,
water never dissolve
the moremolecules of an added
“universal”
surface tension is caused by the
substance;
reason is the SPEED only liquids
with which can.molecules move;
liquid intermolecular attractions among the
faster and MORE FREQUENT interactions with solute
E. Solids molecules in the liquid and that the surface
particles meanshave lower
greater shear viscosities
dissolution ability. than liquids
so they cannot dissolve added substances. tension of water is larger than that of most
other liquids at room temperature.

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THROWBACK: MACROSCOPIC MEASUREMENT: MACROSCOPIC MEASUREMENT: Surface Tension
Compressibility
The compressibility of a substance is an
interesting property. By definition:
compressibility: the fractional DECREASE
in volume per unit increase in pressure.

The capital Greek letter kappa, , is used to


denote compressibility as follows:

V
1  V  −
 =−  =
V
P
V  P 
Surface tension, as we’ve noted, gives water
The idea is that a sample with a volume V is droplets their spherical shape especially in
subjected to some change in pressure, P , the presence of air. One way to further
and the resulting change in volume,  V , is understand this is that surface tension causes
measured. the SURFACE OF THE WATER DROPLET to
behave like a weak, elastic skin.
5 Compressibility
a What is the magnitude of the compressibility of a If we ELIMINATE GRAVITY (think
substance that experiences a drop in volume from 2 astronauts in a space craft floating
volume units to 1 volume unit because of an around), we observe that liquids FLOAT
increase in pressure of 5 units?
AROUND as spherical drops.
A. 1 V 1− 2
− − 7 Surface Tension
` B. 0.1 K= V = 2 = 1 = 0.1 P −1
P +5
C. 0.2
10 a Why are spheres the natural shape for liquid
droplets that experience “internal surface tension?”
D. 0.05
A. Surface tension is not sufficient to create
E. 0.5
“cubes” of liquid which are actually more natural
V 1 − 4 than spheres.
= = 0.75
True or False B. Spheres contain the smallest volume for the
V 4 `
T The fractional decrease in volume for smallest surface area of any geometric shape.
compressibility in which a volume drops from 4 to 1 C. Spheres contain the smallest volume for the
is 0.75 largest surface area of any geometric shape.
D. Spheres contain the largest surface tension for
6 Compressibility the smallest surface area of any geometric
a If L, G, and S represent the compressibilities of shape.
liquids, gases, and solids, respectively, which of the
following is most accurate? E. Spheres contain the largest volume for the
smallest surface area of any geometric shape.
The only choice that makes sense
A. L > G = S is D. Gases are the MOST
` B. L > S = G COMPRESSIBLE and while liquids True or False
(L) and solids (S) might not have
C. G > S > L identical compressibilities, they T Surface tension explains why water drops do not
are close enough for D to be the completely “spread out” or “flatten” on a surface.
D. G > L = S only choice that makes sense.
E. S > L = G

True or False
T Liquids and solids are basically incompressible.

MCAT PREPARATION – CHEMISTRY


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MACROSCOPIC MEASUREMENT: Surface Tension THROWBACK: MACROSCOPIC
We can better appreciate surface tension with MEASUREMENT: Thermal Expansion
the following figure: Thermal expansion is defined as follows:
thermal expansion: the fractional
INCREASE in volume per unit increase in
temperature.
The lowercase Greek letter, , is used to
denote the coefficient of isothermal
expansion as follows:
1  V 
=  
V  T 
We’ve already mentioned that surface tension
results from the intermolecular attractions
9 Thermal Expansion
among the molecules in the liquid. In the figure
above, we see that IF THE LIQUID IS TO a The isobaric coefficient of thermal expansion of a gas
that initially occupies a volume of 4 units and then
INCREASE ITS SURFACE AREA, it would have to expands to occupy a volume of 5 units after a
“redistribute” some of the inner molecules TO temperature increase of 1 K is
THE SURFACE BOUNDARY. This happens, but
the surface area DOES NOT INCREASE MUCH A. 0.5 K
because: ` B. 0.25 K
VICTORIA, PLEASE READ CAREFULLY
C. 0.25 K-1
(re-read if need be):
Molecules at the EDGES have NO D. 0.50 K-1
NEIGHBORS one one side and subsequently E. 4 K-1
experience attractions ONLY FROM
MOLECULES in the bulky interior of the Note: PV = nRT
10 Thermal Expansion
liquid beneath it. In a sense, these “EDGE
MOLECULES” are pulled inward and end up a An ideal gas initially at 0 oC that is heated to 2 oC
would experience what approximate increase in its
as the LINING or BORDER of a “CURVED” or volume? (K = C + 273.15)
“SPHERICAL” SHAPE! Furthermore, those
“EDGE MOLECULES” have a larger A. 9%
POTENTIAL ENERGY than the interior ` B. 7%
molecules.
C. 273%
8 Surface Tension D. 0.72%
a Which of the following is most accurate about the E. 7.2%
spherical shapes of liquid droplets when surrounded
by a gas phase exterior (i.e. air)? ----------------------------------------------
11 RANDOM
A. Energy is released as the surface area of the
droplet is increased. a The n = 4 shell of an atom can hold a maximum of
` B. Surface tension increases as the droplet A. 64 electrons
becomes more spherical.
` B. 32 electrons
C. Energy is required to increase the surface area
C. 24 electrons
of a liquid droplet.
D. 8 electrons
D. The gas phase exterior heats up the droplet,
causing it to become spherical. E. 6 electrons

E. Energy is required to decrease the surface area


of a liquid droplet.

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Vic, based on your understanding thus far, wrap up this PrePacket with the following Fill-
in-the-Blanks paragraph and the WORD BANK provided:

WORD BANK a “multiplier” indicates the word is used THAT MANY TIMES throughout the paragraph.

volume SEPARATIONS forces solids neighbors negligible temperature


attractive tension room GREATER freely STRONGEST gases
condensed (x2) expansion external rigidity vibrate intermediate arrangement
exist resists Thermal intermolecular larger boundaries low

Thermal expansion coefficients of liquids and solids are much smaller than those for gases.
For example, heating water from 20 oC to 21 oC increases its volume by only 0.0212%. This
SIGNIFICANT DIFFERENCE in thermal expansion between condensed states (solids and
liquids) and gases is justified by strong intermolecular forces in condensed states.
With gases, the MUCH GREATER INTERMOLECULAR SEPARATIONS lead to much weaker
forces (in fact, the gas molecules are so far apart that attractive forces are essentially
negligible). In contrast, INCREASING the volume in a solid or a liquid requires that attractive
forces between each molecule and its neighbors be overcome. Because the intermolecular
distances in a solid or a liquid fall in the range where the intermolecular attractive forces are
STRONGEST, relatively small thermal expansion occurs when the temperature of a solid or
liquid is increased.
CONCLUSION: The SAME temperature increase produces much GREATER EXPANSION in a
gas than in any condensed phase.
--------------------------------------------------------------------------------------------
In liquids, molecules are free to travel through the sample, changing neighbors constantly in the
course of their diffusive motion. This “freedom of movement” suggests that liquids have low
shear viscosity, so its molecules can quickly “change neighbors” as the liquid FLOWS in
response to an external stress.
In solids, the molecules do not freely move as they do in liquids but they do constantly
vibrate about their equilibrium positions – they remain quite close to each other. This rigidity of
the solid suggests, in contrast to liquids, that a durable arrangement of neighbors about any
given molecule exists most of the time in the solid phase.
This durable arrangement of molecules in a solid, as opposed to the FREEDOM OF
MOLECULES to diffuse more readily in a liquid, is the critical difference between the solid and
liquid states. In the end, as far as STRUCTURE goes, a liquid is essentially an intermediate
between a gas and a solid.
--------------------------------------------------------------------------------------------
Surface tension and its NATURAL EXISTENCE is somewhat of a surprise to the student of
chemistry (and biology and physics). Consider this:
Phases (gases, liquids, solids) often co-exist. The boundaries between these phases is of
special importance in chemistry and biology. Each boundary has its own UNIQUE
characteristics.
It turns out that the SURFACE OF THE LIQUID resists attempts to increase its area (it just
does NOT want to increase).

The spherical shape of the water droplets is caused by surface tension. We will soon
understand more intimately that surface tension is caused by the intermolecular attractions
among the molecules in the liquid and that the surface tension of water is larger than that of
most other liquids at room temperature.

MCAT PREPARATION – CHEMISTRY


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