Midterm Test Flashcards

1
Q

Wavelength (lambda)

A

Distance between two peaks or two roughs (measured in m or nm)

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2
Q

Frequency (v, nu)

A

Number of waves that pass through a given point . (units S-1, HZ)

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3
Q

Constructive vs deconstructive

A

Waves interfere, do not need to be the exact same.

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4
Q

E = h*v

A

h = Plank’s constant (6.626*10^-24 J/S
E = E photon (= E binding + KE)
V = frequency

= hc/wavelength
C = constant (3x10^8 m/s)

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5
Q

Diffraction

A

Electrons diffract.

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6
Q

Emission of light from atoms

A

Passage of electricity through gas of atoms causes atoms to emit light.

  • Only see 4 frequencies on the detecting screen
  • Discrete emission lines can only be explained by quantisation of the energy levels of atoms and molecules
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7
Q

Schrödinger model of the atom

A

H * Ψ = E * Ψ

H = hamiltonian
E = energy
Ψ = wavelength or orbital = a mathematical function describing the shape of a wave
Ψ^2 = Probability of finding and electron at any point around the nucleus,eaus

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8
Q

Quantum Numbers of Atomic Orbital

A
  1. Principle quantum number (n) - size of orbital
  2. Angular momentum quantum number (l) = (n-1)- shape of orbital
  3. Magnetic quantum number (ml or m) - orientation of orbital (-l <-> +l)
  4. Electron spin quantum number (ms or s) = +/- 1/2
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9
Q

Radial probability

A

Distribution, sum of all Ψ^2

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10
Q

Schrödinger model: Energies of orbitals

A

HΨ = EΨ

E_n = -2.18x10^-18 J *(1/n^2) -DOES NOT depend on l or m

  • Subshells have the same energy (they are degenerate)
    E = how stable the orbital is having the probability Ψ
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11
Q

Pauli exclusion principle

A

No two electrons in an atom can have the same value of all 4 quantum numbers

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12
Q

Factors determining an atom’s energy

A
  1. Electron-nucleus attractions
  2. Electron-electron repulsions - electrons further from the nucleus are shielded from full + nuclear charge by electrons closer to nucleus

Zeff = “effective” nuclear charge
= Z actual - shielding electrons

Ens < Enp < End < Enf
<——– higher zeff

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13
Q

Hund’s Rule

A

If two or more degenerate orbitals are available, one electron goes into each until they are half full. All half fulled orbitals have the same spin quantum number.

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14
Q

Non-directional solid

A

Ionic solids form because oppositely charged ions are attracted to each other in all directions.

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15
Q

Electronegativity

A

The ability of an atom in a molecule to attract electrons toward itself.

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16
Q

Types of Bonding

A
  1. Non-polar covalent (En difference = 0) i.e. H2 - Electronically symmetrical
  2. Polar covalent (En difference <=2.0) i.e HF - partial charges
  3. Ionic (En difference >=2.0) i.e. LiF - full charges, metal + non-metal
17
Q

VSEPR Model

A
  1. Linear (180º - 2)
  2. Trigonal Planar (120º -3)
  3. Tetrahedral (109.5º - 4)
  4. Trigonal Bipyramidal (90º and 120º - 5 “seesaw”)
  5. Octahedral (90º - 6)
18
Q

Dipole Moment

A

A measure of the separation of charge in a molecule arising from the unequal sharing of electrons in polar bonds.

No dipole moment = non-polar
Permanent molecule = polar

19
Q

Ion-dipole Interaction

A

(only for mixtures)
Interaction between fully charges ion and partial charges of a polar molecule
- The energy of attraction increases with the charge of the ion and decreases with the square of the distance between ion and dipole

20
Q

Dipole-dipole interaction

A

Polar molecules attract one another when they orient with unlike charges close together, but they repel one another when they orient with like charges together.

21
Q

Hydrogen-Bonding

A

Dipole-dipole interactions between H and very electronegative elements N and O. I.e. DNA nucleotide base pairs.

22
Q

London dispersion forces

A

Occurs between all molecules, strength depends on size, polarisability.

23
Q

Pressure

A

Force exerted per area
P = F/A

Units Pa = N/m^2; kPa = 10^3 Pa
1 atm = 760 mmHg

24
Q

Kinetic Molecular Theory

A
  1. Gases made of tiny particles moving completely randomly
  2. Total volume of particles very small compared to size of container
  3. Particles do not interact with each other
  4. Particle collisions are elastic
  5. Kinetic Energy increases with temperature
25
Q

Effusion

A

Escape of a gas through a hole into a vacuum

26
Q

Crystalline Solids

A

Well-ordered matter within the solid arrangement of atoms in the solid repeats solids.
4 types: molecular, ionic, covalent network, metallic

27
Q

Amorphous Solids

A

Don’t have extensive ordering of particles.

28
Q

Allotropes

A

Different structural forms of an element.

29
Q

Covalent Network Solids

A

extended structure of atoms held together by covalent bonds.

30
Q

Metallic Solids

A

Metal atoms as cations in sea of “delocalised” electrons.

31
Q

Ionic Solids

A

Held together by electrostatic attraction between cations and anions.

32
Q

Cohesive vs adhesive forces

A

Cohesive: Between molecules (IMFs)
Adhesive: Between molecules and container walls.

33
Q

Colligative Properties

A

Solution properties that depend on concentration of solute, not its identity.

34
Q

Osmotic Pressure

A

Pressure that must be applied to a solution to prevent osmosis from a sample of pure solvent.

35
Q

Vapor pressure

A

Non-volatile solutes decrease vapour pressure of solvent.

Raoult’s Law for non volatile solute:
P = XPº
P = vapor pressure of solvent
X = mole fraction of solvent
Pº = vapor pressure of pure solvent