Unit 3 Flashcards

1
Q

What happens to energy transfer when both atoms’ electronegativities are relatively high?

A

The energy input needed is great. This lessens the magnitude of the electronegativity partial charge distribution. (x(A) - x(B))/(X(AV))

High difference = ionic bond
Low difference = covalent bonding

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2
Q

What is the most stable configuration for covalent bonds?

A

When electrons are delocalized between the two atoms in question.

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3
Q

What does it mean when covalent bonds are directional?

A

It refers to the orientation of atoms when they bond. In essence, the electron fields of covalently bonded atoms are highly directional because the atoms are shared, so they get distorted.

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4
Q

Why can’t atoms form giant networks of bonds?

A

Because each atom is constrained by the amount of bonds it can make, and the high directionality.

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5
Q

What factors influence IMF strength?

A

Polarizability, molecular polarity, and bond polarity

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6
Q

Polarizability

A

The extent to which charge distribution in an atom or molecule is affected by the presence of other charged particles. Inversely related to electronegativity.

Larger molecule = higher polarizability, lower volatility
Smaller molecule = lower polarizability, higher volatility

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7
Q

What is the magnitude of polarizability affected by?

A

The number of electrons and the relative size. Bigger particles mean electrons are further away from nucleus. First refer to the electron quantity of the molecule. A large quanitity of electrons reflects an inability of the nucleus to hold on to the charge dispersion. Think: large surface area = large polarizability

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8
Q

Dispersion forces

A

When two atoms approach each other, attractive/repulsive interactions create a net force that ‘polarizes’ the particles, if only temporarily. This is an ‘induced’ dipole moment. Other name: Van der Waal’s forces - KEY PART OF IMFS FOR NON-POLAR SUBSTANCES

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9
Q

Strength of dispersion forces is related to

A

The product of the polarizabilities of the interacting substances

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10
Q

Dipole-dipole forces

A

IMFs resulting from the presence of permanent dipole moments in molecules, wherein oppositely charged ends of a molecule orient themselves as such to be most attracted - directional bonds

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11
Q

What kinds of molecules have dipole-dipole interactions?

A

Molecules that are polar and have preexisting charges due to a permanent dipole moment

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12
Q

Rank these molecules in order of volatility: CCl4, CBr4, CF4

How is volatility related to molecular size?

A

Since volatility is the ability of a molecule to change state, you can assume that higher volatility means lower change of state points. Simultaneously, a larger molecular size means the hold on outer electrons will be weaker, and polarizability will be greater. Consequently, larger molecules are the least volatile, since they will have stronger IMFs due to the polarizability of its constituents.

Answer: CBr4, CCl4, CF4

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13
Q

What does the magnitude of dispersion forces determine?

A

Among other things, it determines many of a substance’s physical properties, like melting/boiling point, surface tension, and viscosity.

(0.05-40 kJ/mol)

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14
Q

Why are dipole-dipole forces ‘directional’?

A

Since the IMF is created on the basis of electrostatic forces of one molecule interacting with those of another, their strength depends on the orientation of the interacting particles.

(5-40 kJ/mol), but less than 20% of total IMFs

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15
Q

Hydrogen bonding

A

IMFs created on the basis of bond polarity, where Hydrogen atoms are covalently bonding to Nitrogen, Oxygen, or Fluorine atoms, and another N, O, or F atom

This results from a large difference in the electronegativities of the respective molecules involved in interactions.

(10-40 kJ/mol) = strongest IMF

directionally oriented bond

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16
Q

How many different configurations/arrangments can H bonding occur?

A

Considering how few molecules can be involved, there are very few. However, once an interaction is created, the molecules will likely stay together unless enough energy is provided to break these bonds.

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17
Q

How does branching affect IMFs?

A

Branching is highly situational. While straighter and longer molecules have more surface area with which to bond to other molecules, longer branching polymers can cause higher levels of entanglement, increasing viscosity and boiling/melting points.

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18
Q

What two factors is miscibility dependent on?

A
  1. The relative strength of the particles bonding to themselves, then to each other. The particles will adopt a state where the IMFs are strongest, representing lower PE.
  2. # of configurations, wherein the particles adopt a state of higher configurations.
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19
Q

Dipole-induced dipole interactions

A

IMF where a non-polar molecule is polarized by the presence of a polar molecule.

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20
Q

Ion-induced dipole

A

IMF where a non-polar molecule is polarized by the presence of an ionic compound

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21
Q

Ion-dipole

A

IMF where a polar molecule interacts with an ionic compound

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22
Q

Macromolecules

A

Large substances that have properties dependent on their functionality and the structure at different scales

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23
Q

Monomers

A

Repeating unit structures that bond to create polymers/macromolecules

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24
Q

[] (sub n)

A

Inside the brackets is the structure of the monomer, subscript represents how many monomers there are.

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25
Q

How can we predict physical properties of a substance?

A

Analyze the composition, structure, and functional groups of the substance - IMFs may be present, and have a high impact on the properties of the substance

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26
Q

Polyamides

A

Carboxylic acid and amine groups create a rugged and strong substance

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27
Q

Polyesters

A

Carboxylic acid and alcohol groups

28
Q

How does the length of the macromolecule and presence of branching affect shape?

A

It effects the efficacy of IMFs. Short branching means less entanglement, so weaker IMFs.

29
Q

Saturated fats

A

Fats which are ‘saturated’ with hydrogen molecules, and thus have no double bonds, making it a straight molecule. Therefore, IMFs are stronger, and they have high melting points.

30
Q

Unsaturated fats

A

Fats which contain double bonds between Carbon molecules, creating a bent structure in the tail section of the lipid. This weakens the IMFs.

NOTE: the presence of multiple double bonds further lowers melting point because the structure is more and more bent.

31
Q

How does length of fatty acid related to melting point?

A

Since longer carbon chains mean molar mass, there are also more IMFs present, meaning longer molecules have higher melting points.

32
Q

How does branching affect viscosity?

A

Short branched molecules have low viscosity, while longer branched molecules have higher viscosity because the branches cause them to get tangled easier.

33
Q

Protein

A

A monomer-based structure composed of amino acids, which contain a central carbon attached to an amine group, a carboxyl group, an R group side-chain that determines the identity of the monomer, and a single Hydrogen atom

34
Q

Low-density Polyethylene vs high-density polyethylene

A

Low density Polyethylenes are highly branched, thus making them more weakly bonded together, causing the melting point to be lower. However, high density polyethylenes are flatter and straighter, meaning the IMFs are much stronger, creating a high boiling point.

35
Q

How is potential energy affected by the presence of interactions of similar strength?

A

It is lowered. Like with like - i.e. induced dipole-induced dipole, dipole-ion, dipole-dipole

36
Q

What do longer hydrocarbon chains do for a fat?

A

Since there is more surface area, it means there is more room for IMFs to take place, which raises the melting point.

37
Q

Ionic compounds

A

Result from the combination of metal and nonmetal atoms - larger difference of electronegativities between these two atoms

38
Q

The larger the electronegativity difference between bonding atoms, the more ______ the bond.

A

Polar

39
Q

If the EN difference >2, what happens to the bonding electrons?

A

They spend their time closer to the nonmetal atom, leading to an ionic bond.

40
Q

What is the most stable solid-state structure of ionic compounds?

A

Crystal lattice

41
Q

How does temperature affect the structure of ionic compounds?

A

It stabilizes the properties of the substance by solidifying it into the crystal lattice form

42
Q

Are electrons fully transferred to the more electronegative atom?

A

No, but it’s really close considering the electronegativity differences. Consider the ionic character.

43
Q

Ionic compound naming (simple)

A

metal name + (nonmetal name & -ide)

*add roman numerals if necessary

44
Q

Hydrate naming

A

Metal name + (nonmetal & -ide) + (prefix & hydrate)

45
Q

Hydroxide

A

OH-

46
Q

Nitrate

A

NO3-

47
Q

Carbonate

A

CO3(2-)

48
Q

Sulfate

A

SO4(2-)

49
Q

Phosphate

A

PO4(3-)

50
Q

Ammonium

A

NH4+

51
Q

Peroxide

A

O2(2-)

52
Q

-ate vs -ite

A

‘ate’ compounds have one more oxygen than ‘ite compounds’, but maintain the same charge

53
Q

Face-centered cubic structure

A

Ions occupy the corners and center of each face of the cube

54
Q

Body-centered cubic

A

Ions of the same charge occupy only the corners, while opposite charge is at the direct center of the cube

55
Q

True or false: cations are smaller than anions

A

True: because cations are losing electrons, it vacates the outer shells, decreasing electron repulsion and pulling electrons in towards the nucleus.

56
Q

Coulomb’s Law

A

Tells us the relative strength of the bond between ions

Higher charges or smaller ions = higher electrostatic forces

F = K(q1)(q2)/(r^2)

r = distance between bonded particles
(q1 and q2) = charges of atoms involved
K = Coulomb’s constant (8.9 x 10^9 Nm2/C2)

57
Q

Why are ionic compounds not conductors when solid?

A

The electrons in an ionic compound are ‘localized’ to an ion based on polarizability and electronegativity differences. In the molten state, the heat overcomes the strength of the bonds, allowing the electrons to ‘delocalize’ more effectively.

58
Q

What are ‘strong electrolytes’?

A

Soluble ionic compounds that completely dissociate into free ions when immersed in water

NaCl(s) +H2O(L) => Na+ (aq) + Cl- (aq)

59
Q

What are ‘weak electrolytes’?

A

Slightly soluble ionic compounds that barely dissociate, and don’t conduct electricity.

60
Q

What is solubility of ionic compounds determined by?

A
  1. Net interactions between ions and water molecules should be stronger than net interactions between the ions themselves. (mixed/dissolved has lower PE)
  2. The number of configurations that the ions and water molecules can adopt when mixed is larger than the total number of configurations they can have if they do not mix. (mixed/dissolved has more configurations)

If only one of these conditions is met, the outcome will depend on which competing factor is dominant. Solubility varies with temperature.

61
Q

Why are smaller charges more favorable for dissolution?

A

Small charges don’t generally constrain the configurations that surrounding water molecules can adopt.

62
Q

How does ion size affect solubility?

A

Larger ions are more soluble, as demonstrated by Coulomb’s Law. Though larger ions may be less attracted to water molecules, the large size increases the amount of configurations the ion can occupy. Simultaneously, as ion size gets larger, ions requires less energy to dissociate.

Ion- H2O dipole IMFs are dominant

63
Q

Why are insoluble compounds in solution poor conductors?

A

Because very few of the ions have dissociated, charge is not distributed across the system.

64
Q

Product rule

A

If the ion charges of each ion have a product of less than 4, then the compound is soluble in water.

65
Q

Components of amino acids

A

Central carbon bonded to carboxyl group and amine group, a hydrogen, and an R group that determines its identity - about 20 of them