Structure IB Flashcards

(59 cards)

1
Q

Principal energy levels

A

N=1 closest to nucleus has lowest energy

Electrons in each energy level =2n^2

Main energy levels are split into sub levels
•n=1 (1s)
•n=2 (2s, 2p)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Isotope properties

A

Same chemical properties cuz e- count stays the same

Diff physical properties cuz neutron count is diff

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Aufbau principle

A

Fill lower energy levels before higher ones

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Pauli exclusion principle

A

Atomic orbital can hold 2e- with opp spins

Have to pair electrons in one level before putting electrons in next

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Hund’s rule

A

In sub level fill each degenerate orbital with electrons with single parallel spin electrons before pairing them in that degenerate orbital

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

S orbital

A

Spherical has max 2 electrons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

P orbital

A

Has 3 degenerate orbitals (Px Py Pz)

Each degenerate can hold 2 so 6 total electrons

Dumbbell shaped

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Flame test

A

Identified metal ions in solution

Heat causes e- to absorb energy and transition to higher energy level. As they emit energy they go back to their og state and the energy emitted corresponds to a wavelength

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Line Spectra’s

A

Continuous- all wavelengths
Absorption- black lines on coloured background
Emission- coloured lines on black background

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Ionization energy

A

Energy needed for electrons to move from n=1 to n=infinity

First IE is energy needed to remove 1mol of e- from 1 mol of gaseous atom to produce a cation and e- (endothermic)

Increases across period (nuclear charge increases and atomic radii decreases so more energy needed)

Decreased down group (with more energy levels, valence e- are farther from nucleus and easier to remove

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Electron Sheilding

A

Inner e- shield outer valence e- from full attraction to nuclear

Constant across period
Increases down a group

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Effective nuclear charge

A

Net positive charge experienced by valence e-
Atomic number - shielding electrons
Constant across group
Increases left to right

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Trends in atomic radii

A

Decreases across period
Increases across group cuz more energy levels occupied
Nuclear charge increased across period
As atomic radii decreases attraction between nuclear and outer electrons increases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Trends in ionic radii

A

If attraction between nucleus and outer e- increases than ionic radii decreases

Cations are smaller than parent atom cuz they lose e- while anions are bigger cuz they gain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Electronegativity

A

Increased across period
Decreased down group as bonding electrons are farther from the nucleus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Metallic character and metallic binding

A

MC- how easily atom can lose e- (increases down group decrease left to right)

MB-electrostatic attraction between lattice e of cations and delocalized e-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Electron affinity

A

Opposite of ionization energy so it’s the energy released adding electrons to atom to make it anion (exothermic)

Greater the atomic radii means greater number of shielding e- =decrease in affinity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Transition element

A

Atom w incomplete d-sub level (zinc is not transition metal cuz it has complete d sub level)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Complex ions

A

Contains central metal ion and ligands (have lone pairs that can form coordinate covalent bonds (both electrons in bond come from same atom))

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Determining charge if complex ion

A

If ligands are neutral than complex ion has same charge as central metal

If negative than subtract total charge of ligands from the charge of the metal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Coordination componds

A

Contain the complex ion and a counter ion to balance the charge of complex ion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Resonance structures

A

More than 1 position for double bind in molecule

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Allotropes

A

Diff physical forms of the same element (carbon can be diamond graphite )

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Difference IMF’s

A

LDF- movement of electrons
DD- electrostatic attraction between partial positive and negative
H bonding- H to NOF

25
Ion dipole
Force between ion and oppositely charged ends of water forming a hydration shell
26
Crystal Field Theory
Splitting- ligands approach central ion causing repulsion between ligand lone pairs and electrons in d orbital of central ion Unequal repulsion causes splitting Electrons in lower d orbital can absorb energy and transition to higher d orbital- the opposite of the colour of wavelength absorbed is the colour observed
27
Factors that affect colour of complex ion
Oxidation state- higher OS = higher energy difference between d orbitals so wavelengths absorbed decreases Identity of central ion and ligands
28
Stereochemical series
Ligands orders by their ability to split of d orbitals increase left to right
29
Magnetism
Magnetism increases and number of unpaired electrons in 3d increase
30
Alloys
Non direction bonding
31
Sigma bond
Head on overlap of atomic orbitals Electron density is concentrated
32
Pi bonds
Sideways overlap Election deputy is above and below the plane of nuclei
33
Hybridization
Mixing of atomic orbitals Electron density
34
Avogardo rule
At same temp and pressure equal volumes of gas have the same number of particles
35
Real gas behaviour
Donate measurable energy lost so non elastic collisions Volume is significant Acts like ideal gas at high temp and low pressure
36
Lattice enthaply
Enthalpy change when 1 mol of solid ion is broken into its consistent gases
37
What increases lattice enthalpy
Small atomic radius bcz electrostatic attraction is stronger Higher charge for same reason
38
Delocalised pi electrons
Free to move and conducts electricity Shared between multiple nuclei
39
Homologous series
Differs by common structural u it
40
What happens to BP and molar mass increases
Number of electrons increases=kore Polaris able=higher LDF=higher BP
41
Branched chain Isomers
Lower BP than straight chain cuz less SA contact so lower LDF
42
Structural isomers
Chain- branch vs straight Positional- func group in diff positions Func group- diff functional groups
43
Cis trans isomerism
Restricted rotations around carbon double bind due to pi bond Same is cis Diff is trans
44
Optical isomerism
Chiral molecule w carbon bonded to 4 diff substitutes
45
Entropy
Ways of arrangement
46
When is entropy spontaneous
When greater than 0
47
What Gibbs Ecell and K value suggest spontaneous
- + Large
48
Conditions for successful reaction
Correct orientation Collisions w energy greater than activation energy
49
Rate determining step
Step w greater EA
50
Rate
=k[A]^x[B]^y Where k is rate constant A and B are concentrations And x and y are orders (x+y=overall order)
51
How to determine order
Changing concentration has no effect that zero order Directly proportional than first order Square of change than second order
52
Units of k (use overall order
Zero: mol dm-3 s-1 First: s-1 Second: mol-1 dm3 s-1 Third: mol-2 dm6 s-1
53
Q and K
Same equation (p/r) but q uses concentrations and k use equilibrium concentrations Q less than k than right
54
Bronsted Vs Lewis
BA- proton donor (LA- electron acceptor) BB- proton acceptor (LA- electron donor)
55
Acid rxns
Acid + metal hydroxide/ oxide= salt and water Acid + metal carbonate/ hydrogen carbonate= salt water carbon dioxide
56
Disproportionation
Both oxidized and reduced
57
Primary vs secondary cell
P- not reversible S- rechargeable and Reversible w electricity
58
Homolytic vs heterolytic bond fission
Homo each takes one electron Hetro more electronegative on takes the election
59
Rxn pathways
P alcohol (Cr2O7^2-/H+ and Heat distillation )= aldehyde P alcohol (Cr2O7^2-/H+ and heat reflux) = carb acid S alcohol (Cr2O7^2-/H+ and heat) = ketone Ketone to S Alcohol (NaBH4 and H+) Carb acid to P alcohol (LiAlH4 and H+) Aldehyde to P alcohol (NaBH4 and H+)