11A - Intermolecular Forces Flashcards

1
Q

Def: What is a phase? What are the 3 (or 5 if you’re smart) kinds.

A

Physically distinct, homogeneous part of a system comprised of one physical state of matter:
1. BE Condensates
2. Solids
3. Liquids
4. Gases
5. Plasmas

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2
Q

Def: What are the two types of energies that the states are dependent on the balance between?

A

EP: Potential energy or stored energy, which in the form of attractive forces draws particles together
KE: Kinetic energy, the energy of motion which tends to disperse particles

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3
Q

Def: What is temperature, and what is it in relation to Avogadro’s number, R, and average energy per mol.

A

Average KE of group of particles.
T = (2/3) (Na/R) (0.5mu^2)
R = 8.3145 J/mol*K

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4
Q

Def: What two things are thermodynamics of phases dependent on the balance between?

A

Enthalpy: Transition btw phases and interruption of IMFs due to q changing, but T remaining constant at phase change
Entropy: Increasing disorder in a system through increasing phase changes

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5
Q

Theory: Describe the shapes, volumes, compressibility’s, and flows of solids, liquids, and gases.

A

Solids: Fixed shape, fixed volume, incompressible, no flow
Liquids: Variable shape, fixed volume, low compressibility, moderate flow
Gases: Variable shape, variable volumes, highly compressible, high flow

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6
Q

Theory: Explain why, in relation to KE, some phases have higher ability to fill up a container.

A

High KE = high movement = easier to escape neighboring molecules = filling up container more.

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7
Q

Def: What is a phase change?

A

Phase changes involve the forming, breaking or changing the strength of intermolecular forces.

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8
Q

Theory: Explain the effects of KE and IMFs on the phase of a substance.

A

KE: Keeps particles moving, apart.
IMFs: Attraction, keeps particles together.

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9
Q

Def: What is an IEMF? How do they compare to bonding forces

A

Intermolecular forces.
Attractive, electrostatic forces that exist between all molecules, ions and atoms.
Relatively weaker.

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10
Q

Def: What are the 3 types of bonding, known as IMFA’s?

A
  1. Ionic: Cation-Anion
  2. Covalent: Sharing of e- pairs.
  3. Metallic: A cation in a delocalized see of e-.
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11
Q

Def: What are the 7 types of IMFE’s?

A
  1. Ion-Dipole: Ionic charge and dipole charge
  2. H-Bonds: A polar bond to H and a dipole charge
  3. Dipole-Dipole (Stationary solids/liquids): Dipole charges
  4. Ion-induced dipole: Ionic charge to polarizable e- clouds.
  5. Dipole-Dipole (Rotating gas): Dipole charges
  6. Dipole-induced dipole: Dipole charge to polarizable e- clouds.
  7. LDF’s: btw polarizable e- clouds.
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12
Q

Theory: How do IMFE’s explain bp, mp, vp, st, viscosity, and capillary action?

A

IMFE’s are all electrostatic, meaning btw + and - species.
More IMFE’s means higher bp and mp. Reaching bp or mp means breaking IMFE’s, not IMFA’s. All other properties are affected somewhat by IMFE’s

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13
Q

Def: What is r?

A

Distance across which EP (attractive interactions) interaction are felt.

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14
Q

Def: Why is there a limit on how close molecules can be, and what is it? At what distance do interaction rapidly fall of.

A

There is a limit as at short distances, repulsive forces will dominate. For LDF’s, it’s 1/r^12 At about 1/r^6 , interaction falls of.

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15
Q

Def: Define ion-ion interactions. What is their effect, and comment on their directionality. What is the EP equivalent to?

A

Oppositely charged ions attracting.
1/r
Non-directional.
Crystal lattice energy, where ions form extended repeating units.

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16
Q

Def: Define ion-dipole forces. What is their effect, and what is hydration? What major property of ionic compounds does this interaction largely determine.

A

Attraction between oppositely charged dipole end and ions.
1/r^2
Attraction of water dipole (permanent) to ion.
Solubility.

17
Q

Theory: Explain the effects of cation size and cation charge on hydration of salts.

A

Smaller cations = stronger ion-dipole = more hydration and vice versa
Higher ionic charge = stronger ion-dipole = more hydration.

18
Q

Def: What is mu (the u letter thing).

A

A permanent dipole.

19
Q

Def: Define dipole-dipole and dipole moments. What is their effect(s).

A

Molecules will arrange themselves into lowest energy, least repulsive config. The permanent dipoles adds to the attractive forces btw molecules. These dipole moments cause d-d interactions.
When dipoles are in the same direction, 1/r^3.
When averaged over all possible orientations (rotating gases tend to move), 1/r^6.

20
Q

Theory: How do dipole-dipole affect bp.

A

Magnitude of dipole moment is one of the main factors affecting bp. Dipole moments increase with polar.

21
Q

Def: Define h-bonds. How do they affect bp and mp. How do they compare to chemical bonds.

A

Strong IMFE’s, very electronegative atoms to exposed H (not shielded by electron, just a proton). Higher bp and mp. Only about 2-5% as strong as chemical bonds.

22
Q

Def: Define dipole-induce-dipole. What is the effect and why.

A

Polar mol can interact with non-polar molecules to induce a dipole.
1/r^6, as molecules must be close to induce dipole.

23
Q

Def; What is an induced dipole, and what is its strength based on?

A

The distortion of a usually symmetrical electron cloud.
Related to polarizability of the molecule and strength of inducing charge of dipole.

24
Q

Def: What is an LDF. What is their effect.

A

Motion of e- in atoms can cause unequal e- distribution resulting in instantaneous dipoles. These dipoles interact temporarily, having their effect reverse every 10^-16 seconds. Exist in all molecules.
1/r^6

25
Q

Theory: Despite being inert, noble gases can exist as liquids if cold enough. Why?

A

LDF’s can keep particles together at low temps.

26
Q

Def: What is polarizability? How does it change going through the periodic table and why? What is the relationship btw particle size and polarizability?

A

Ease with which the e- cloud is distorted.
Increase down a group as atomic size increase, meaning larger e- clouds which distort more easily.
Decrease across a period, as ENC increase.
Smaller particles = electrons held more tightly = less polarizable.

27
Q

Theory: What 3 properties most affect LDF’s.

A

Increasing size will increase LDF’s.
Increasing polarizability will increase LDF’s.
Increasing area of interaction will increase LDF’s.

28
Q

Theory: What is the general rule, and 3 other rules for comparing IMFE’s.

A

General: For molecules of same mass and size, IMFE’s increase with polarity.
1. LDF’s always present
2. If similar shapes and #e- btw molecules, difference in magnitude of IMFE’s is dependent on D-D and other kinds (not LDF’s).
3. If molecules differ wildly in #e-, LDF’s are decisive.

29
Q

Theory: What are the 5 rules for assessing LDF’s in molecules.

A
  1. LDF”s always present and become greater in mag w/ increase #e-.
  2. Dependent on shape.
  3. D-D will add to LDF affects and are found in polar molecules.
  4. H-B will do the same a 3, and tend to be stronger than both.
  5. None are as strong as bonding forces.