Inorganic Chemistry Flashcards

1
Q

Electromagnetic spectrum: order

A

RMIVUXG

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2
Q

Electromagnetic radiation in order of frequency

A

GXUVIMR

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3
Q

Electromagnetic spectrum: names

A

Radio, Microwave, Infrared, UV, X-Ray, Gamma

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4
Q

Finding energy using wavelength

A

Energy is in kj. So wavelength (nm) is x10 to power of -9. Answer x10 to power of -3 (milli to 1)

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5
Q

how are lines on a spectrum formed?

A

An electron is promoted to a higher energy level. When the excited electron drops back to a lower level, energy is given off to a corresponding wavelength. DO NOT MENTION ABSORBING LIGHT.

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6
Q

absorption spectroscopy

A

electromagnetic radiation is directed at an atomised sample. radiation is absorbed as electrons are promoted to higher energy levels

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7
Q

emission spectroscopy

A

high temperatures are used to excite electrons, making them drop to lower energy levels, emitting a photon as they do so

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8
Q

atomic spectroscopy: conc. of an element

A

concentration of an element is related to the intensity of light emitted or absorbed

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9
Q

number of electrons found in an orbital

A

max of 2

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10
Q

n

A

principal quantum number, main energy level for an electron

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11
Q

shapes of orbitals

A

s, p, d, f

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12
Q

l

A

angular momentum quantum number. shape of subshell (s, p, d)

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13
Q

ml

A

orientation of the orbital. -l to +l values

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14
Q

ms

A

direction of spin. +1/2 of -1/2

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15
Q

the aufbau principle

A

electrons fill orbitals in order of increasing energy

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16
Q

hund’s rule

A

electrons fill degenerate orbitals singly and with parallel spins before pairing occurs

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17
Q

the pauli exclusion principle

A

no two electrons in one atom have the same set of four quantum numbers. therefore, no orbital can hold more than two electrons and those electrons must have parallel spins

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18
Q

division of periodic table into s, p, d, f

A

corresponds to the outer electronic configurations of the elements within these blocks

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19
Q

special stability

A

associated with half-filled and full subshells

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20
Q

stability and ionisation energy

A

the more stable the electronic configuration, the higher the ionisation energy

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21
Q

VSEPR

A

valence shell electron pair repulsion theory: used to predict the shapes of molecules and polyatomic ions. electron pairs are negatively charged so repel each other, therefore they are arranged to minimise repulsion and maximise separation

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22
Q

electron pair repulsion strength

A

decrease in order of: non-bonding pair/ non-bonding pair> non-bonding pair/ bonding pair> bonding pair/ bonding pair

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23
Q

transition metal

A

metals with an incomplete d subshell in at least one of their ions

24
Q

copper and chromium

A

have a complete d subshell due to the special stability associated with having the d subshell being half-filled or completely filled

25
Q

transition metals becoming ions

A

the 4s electrons are lost before the 3d electrons

26
Q

oxidation state

A

is the oxidation number

27
Q

oxidation number

A

the sum of all the oxidation numbers of all the atoms in a neutral compound must add up to zero. the sum of all the oxidation numbers of all the atoms in a polyatomic ion must be equal to the charge on the ion

28
Q

oxidation

A

increase in oxidation number

29
Q

reduction

A

decrease in oxidation number

30
Q

oxidising agents

A

compounds containing metals in high oxidation states

31
Q

reducing agents

A

compounds with metals in low oxidation states

32
Q

ligands

A

negative ions or molecules with non-bonding pairs of electrons that they donate to the central metal atom or ion, forming dative covalent bonds

33
Q

ligand classification

A

monodentate up to hexadentate

34
Q

coordination number

A

total number of bonds from the ligands to the central transition metal

35
Q

complex of a transition metal

A

d orbitals no longer degenerate

36
Q

splitting of d orbitals

A

splitting to higher and lower energies occurs when the electrons present in approaching ligands cause the electrons in the orbitals lying along the axes to be repelled

37
Q

strong field ligands

A

create a large difference in energy between subsets of d orbitals

38
Q

weak field ligands

A

create a small energy difference between subsets of d orbitals

39
Q

colours of transition metals

A

explained in terms of d-d transitions. light is absorbed when electrons in a lower energy d orbital are promoted to a d orbital of higher energy

40
Q

heterogeneous catalysis

A

presence of unpaired d electrons or unfilled d orbitals allows activated complexes to form as reactive molecules are adsorbed, providing a reaction pathway with a lower activation energy. therefore, transition metals are often catalysts

41
Q

homogeneous catalysis

A

changing oxidation states with the formation of intermediate complexes

42
Q

Ionic bonds

A

Will form when atoms can rearrange their electrons to produce an arrangement of lower energy. Ionic lattices are more stable

43
Q

Minimising electron repulsion

A

Lone pairs of electrons are always positioned equatorially to minimise repulsion. The shape of the molecule is also supposed to minimise this

44
Q

Bonding pairs

A

Shape is dependent on number of bonded electrons, so answer to formula may not always be right

45
Q

Octahedral

A

6 pairs. 90

46
Q

Trigonal bipyramidal

A

5 pairs. Down 90, across 120

47
Q

Tetrahedral

A

4 pairs. 109.5

48
Q

Trigonal planar

A

3 pairs. 120

49
Q

Linear

A

2 electron pairs. 180

50
Q

Number of electron pairs, formula

A

Number of outer electrons on central atom + number of bonded atoms — charge. DIVIDE ALL THIS BY 2

51
Q

Resonance structure

A

More stable than normal structure. A double and single bond will flip around e.g. ozone

52
Q

Dative covalent bond

A

When one atom provides both of the electrons that form the covalent bond

53
Q

Orbital boxes

A

1s, 2s, 2p, 3s, 3p, 4s, 3d. 4s comes before 3d if it is an ion or transition metal

54
Q

Oxidation number

A

How many electrons have been lost

55
Q

Coordination compound

A

Cation/ anion can’t exist on their own so must have charges balanced. The complex ion will bond with oppositely charged ions to form a complex