Chemistry UNIT 2- Electron configuration and bonding Flashcards

1
Q

What is the Heisenberg Principle?

A

You can’t know with certainty both where an electron is and where an electron will travel to next.
This makes it impossible to plot the orbit and location of an electron around a nucleus.

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2
Q

What is the arrangement of electrons in their subshells up to 4D^10

A

1S^2 2S^2 2P^6 3S^2 3P^6 3D^10 4S^2 4P^6 4D^10

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3
Q

What is the aufbau principle?

A

Electrons fill the lowest energy level subshell first before moving to the next level.

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4
Q

What is Hund’s rule

A

The most stable arrangement of electrons is that with the maximum number of unpaired electrons all with the same spin direction. (one electron goes into a orbital at a time before doubling up)

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5
Q

What is the Pauli Exclusion principle?

A

No two electrons in a atom can have the same set of four quantum numbers in an orbital and they must have opposite spins.

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6
Q

What is ionisation energy?

A

The energy required to remove 1 electron from each atom in 1 mole of gaseous atoms to form 1 mol of gaseous 1+ ions.

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7
Q

What are the main key points for electron configuration?

A
  • Electrons arranged in energy levels (shells) which also themselves have subshells.
  • Each subshell consists of 1+ electron orbital
  • Each orbital can hold 2 electrons with opposite spins
  • Electrons fill lowest energy level orbitals first.
  • Exceptions are Cr & Cu have 4S electrons promoted to 3D
  • Electrons occupy orbitals singularly and only pair up when no empty orbitals of the same energy level are available.
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8
Q

What is successive ionisation energy?

A

To form a positive ion, we need energy to overcome the electrostatic attraction from the nucleus.
A each electron in removed from an atom the remaining ions gain a more positively charged structure so more energy is required.

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9
Q

Complete the first and second ionisation equation for potassium.

A

1st IE: K(g) —-> K+ + e-
2nd IE: K+(g) —-> K2+ + e-

Each time you do a successive ionisation equation, start from the previous IE

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10
Q

What are the main factors affecting Ionisation energy?

A
  • Atomic radius- Greater the atomic radium, smaller nuclear attraction experienced by the outer electrons
  • Nuclear charge- Greater nuclear charge, greater the attraction force on the outer electrons.
  • Electron shielding- Inner shells of electrons repel the outer shell electrons.
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11
Q

What is the general trend in ionisation energy down a group?

A
  • Negative trend due to a greater number of orbitals creating a larger shielding effect which means that IE energy is required.
  • Larger atomic radius so there is less attraction between the positive nucleus and negative electrons.
  • Nuclear charge is greater due to an increase in proton number however more orbitals means more shielding therefore is less effective.
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12
Q

What is the general trend in ionisation energy across a period?

A

The general trend increases the first IE as you go across the period as the is a higher nuclear charge and no extra orbitals causing electron shielding.

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13
Q

What is the explanation across a period for the difference in Group 3 elements?

A

There is a drop in the value of the element. This is because the extra electron has gone into one of the 2P orbitals. This increases the shielding making the electron easier to remove.

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14
Q

What is the explanation across a period for the difference in Group 6 elements?

A

Drop in the value of the element due to the extra electron being paired up with one of the electrons already in one of the 2P orbitals. The repulsive force between the two paired up electrons means that less energy is required to remove one of them.

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15
Q

Why do transition metals have similar ionisation energies bar zinc?

A

All of the elements have an electron structure of [Ar] 3D^n 4S^2. The electron being lost always comes from the 4S orbital.

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16
Q

Which would have the higher value, the 1st IE of sodium or the second IE of magnesium?

A

Magnesium would have the higher IE even though they have the same electronic structure. Magnesium has 12 protons and sodium has 11 therefore there is a greater nuclear charge attracting the electron to be removed in magnesium so a higher ionisation energy is required.

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17
Q

What is the trend for the size of the atomic radius across a period?

A

Number of protons increases which increases the “pull” on each electron, therefore pulling them in closer and reducing the atomic radius.
There is no increase in the number of shells/ energy levels to cause any effective shielding.

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18
Q

What is the trend for the size of the atomic radius down a group?

A

Increase in the number of energy levels/shells which causes a significant shielding effect.
There is a greater number of protons as you go down the group however these protons do not have a significant enough effect to overcome shielding.

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19
Q

What are the factors effecting effective nuclear charge?

A

Number of protons.

Shielding from inner electrons/shells

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20
Q

What is the ionic radius trend in metals and non-metals?

A

Metals- lose electrons when gaining an ion so the electrons left in the atom will feel a greater effective nuclear charge and so the ionic radius is always smaller than the atomic radius.

Non-metals- Gain electrons so the ionic radius becomes larger than the atomic radius.

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21
Q

What is the bonding like in metallic bonding?

A
  • Strong forces of attraction
  • Electrostatic forces of attraction between metal atoms
  • Sea of delocalised electrons and positive ions
  • Regular pattern.
22
Q

What are the properties of metallic bonding?

A
  • Strong (high tensile strength)
  • High melting point
  • Ductile
  • Conductors of heat and electricity
  • Malleable
  • Sonorous
  • Shiny
  • High density.
23
Q

What is the bonding like in ionic bonding?

A
  • Electrostatic forces of attraction between oppositely charged ions
  • Occurs between a metal and non-metal.
  • Giant lattice
24
Q

What are the properties of ionic bonding?

A
  • High melting point
  • Soluble in water
  • Conduct electricity when in solution or molten due to ions being free to move.
  • Crystalline structure.
25
Q

What is the bonding like in covalent bonding?

A
  • Sharing pairs of electrons between atoms that are non-metal.
  • Multiple bonds are possible
    (single, double and triple bonds)
26
Q

What are the properties of covalent bonding?

A
  • Tend to have low melting and boiling points
  • Majority form simple covalent molecules
  • Few form giant covalent structures (eg diamond, graphite, silicon dioxide, fullerenes)
  • Non conductors of electricity
    (except graphite)
27
Q

Define electronegativity

A

A measure of the tendency of an atom to attract a bonding pair of electrons in a covalent bond.

Therefore the greater the electronegativity of an atom the more it attracts electrons towards it.

28
Q

What are the factors affecting electronegativity?

A
  • Distance form the nucleus
  • Atomic charge
  • Electron shielding
29
Q

Define a permanent dipole.

A

The partial charges produced due to differences in electronegativity between two atoms produces a permanent dipole.

30
Q

Define the permanent dipole-dipole force.

A

Dipole-dipole interaction between a slightly positive atom of one molecule and a slightly negative atom of another molecule.
Polar molecules will attract one another with inter-molecular forces of attraction called permanent dipole-dipole interactions

31
Q

What is a dative covalent bond? (co-ordinate bond)

A

Shared pair of electrons provided by one of the bonding atoms.

32
Q

What is a hydrogen bond?

A

They are the strongest form of intermolecular forces and generally occur when hydrogen is bonded to the 3 3 most electronegative (oxygen, nitrogen, fluorine)

33
Q

What factors are needed for a hydrogen bond to form?

A
  • Hydrogen atom bonded to a strongly electronegative atom
  • Lone pair on another electronegative molecule.
  • Must have a hydrogen atom bonded to a nitrogen, oxygen or fluorine atom (NOF’s) and a lone pair.
34
Q

What evidence is there to show the presence of hydrogen bonds?

A

Boiling point trend in groups 5, 6 and 7 when the elements are bonded to hydrogen.

35
Q

Explain the trend in boiling points for the elements in groups 5, 6 and 7 when bonded to hydrogen.

A

Generally the boiling points increase as you go down the group due to the molecules becoming larger and so more intermolecular forces must be broken. An increase in electrons means there are more van der waal forces to overcome on heating. The first elements in each group (N,O,F) have exceptionally high boiling points so there must be extra/stronger intermolecular forces requiring more energy to be broken. (hydrogen bonds)

36
Q

How can a temporary dipole form?

A

Can form due to the constantly changing arrangement of electrons causing fluctuations and shifts in charge across a molecule or atom.
This then affects the distribution of electrons in nearby atoms so they become attracted to the original atom for that instant.

37
Q

How is an instantaneous dipole induced dipole force formed? (van der waals)

A

As the electron distribution of the original atom changes, new dipoles will be induced in neighbouring atoms which will be attracted towards it.

These are van der waal forces.

38
Q

What factor affects the strength of a van der waal force?

A

Size of an atom

39
Q

What are the different types of intermolecular forces?

A
  • Hydrogen bonds- strongest forces must have N. O, F, H and a lone pair.
  • Dipole-dipole interactions- Forms in polar covalent molecules.
  • Van der waals- weakest intermolecular force and can be present between any molecule.
40
Q

What is mass spectrometry?

A

A technique used to determine relative atomic mass of an element.
Separates molecules according to their charge and mass which allows us to identify a sample chemical by measuring its molecular mass.

41
Q

What is the mass charge ratio?

A

How to calculate the mass spectrum.

Mass = mass / Charge (1)

42
Q

What is a time of flight mass spectrometer?

A

A device which substances in a sample are converted into positive ions and accelerated at high speeds. These separate substances will then arrive at a detector at different times depending on their mass/charge.

43
Q

What is the need for a vacuum in a time of flight mass spectrometer?

A

The entire apparatus is kept in a vacuum to prevent the ions produced from colliding with the air.

44
Q

In the time of flight mass spectrometer, how does the ionisation of the sample work?

A

The sample is vaporised and a high energy electron gun fires electrons at the sample. This knocks off an electron from each particle forming a 1+ ion.

45
Q

How does acceleration work in a time of flight mass spectrometer.

A

Positive ions are attracted towards a negatively charged plate. The attractions cause the ions to accelerate towards the plate, so ions with higher charges or ions which are lighter will achieve a higher velocity.

46
Q

What is the ion drift stage in a time of flight mass spectrometer?

A

As the ions pass through a small hole and travel along a tube a beam forms towards the detector.

47
Q

Explain the detection stage in a time of flight mass spectrometer.

A

Ions with the same charges at the detector and ions which are lighter arrive first due to a higher velocity. The flight times are recorded and ions pick up an electron from the detector.

48
Q

How can the data be analysed from a time of flight mass spectrometer?

A

As the ions pick up an electron a current flow sending a signal from the detector to a computer which generates a mass spectrum for the sample.

49
Q

What is VSEPR?

A

Valence Shell Electron Pair Repulsion Theory

A model used to predict the geometry of individual molecules from the number of electron pairs surrounding their central atoms.

50
Q

What do lone pairs do in terms of VSEPR?

A

Lone pairs have a greater repulsive force effect than a bonding pair of electrons.
Lone pairs bend the angles by 1 degree either side of the base atoms pushing off an extra 2 degree angle of repulsion.