Giant Structure Flashcards

(40 cards)

1
Q

Name 3 methods of proving ion existence

A

Electrolysis
Ion migration
X-ray crystallography

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2
Q

How does electrolysis prove ion existence

A

aq/l
Conduct electricity
Free delocalised electrons to carry charge

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3
Q

How does ion migration prove ion existence

A

aq coloured ions
Copper chromate solution soaked paper
Crocodile clips, DC power supply
Blue copper cations, yellow chromate anions

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4
Q

How does X-ray crystallography prove ion existence

A

Diffract through slag crystal
Electron density map
Contours link equal charge regions
Separate ionic solid entities

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5
Q

Lattice energy

A

Energy change to make 1 mole of a solid ionic crystal from its gaseous ions
Exo

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6
Q

Standard enthalpy change of formation

A

Energy change to make 1 mole of a compound from it’s elements in their standard state under standard conditions

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7
Q

Standard enthalpy change of atomisation

A

Energy change to make 1 mole of gaseous atoms from it’s elements in their standard state under standard conditions
Endo

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8
Q

Ionisation energy

A

Energy to remove 1 electron from each atom/ion in 1 mole of gaseous atoms/ions
Endo

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9
Q

Electron affinity

A

Energy change to add 1 electron to each atom/ion in 1 mole of gaseous atoms/ions

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10
Q

Describe the energetics pattern of electron affinity

A

From neutral = exo
From negative = endo
Negative charge of ion and negative charge of electron repel each other, energy must be absorbed to overcome the ESR

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11
Q

Describe the 3 general layers of a borne haber cycle

A

Natural elements
Gaseous ions
Solid lattice

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12
Q

Describe the differences (4) between a BHC of NaCl and MgCl2

A

Higher IEs
Higher No.IEs
Higher lattice enthalpy
Double Cl values

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13
Q

Name 3 factors that effect LE

A

Charge of ions
Size of ions
No. Ions

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14
Q

BHC exam technique terminology

A

X larger/smaller
More Endo/exo
State what is

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15
Q

How does charge effect LE

A

Higher charge
Higher ESA between ions
Higher ETO
More exo LE

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16
Q

How does ion size effect LE

A

Larger size
Ions further away
Less ESA
Less exo LE

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17
Q

Exam technique factors effecting LE

A

State what’s the same and what’s different

18
Q

What’s influences theoretical LE

A

Ion attraction/repulsion

19
Q

How do you calculate the theoretical LE

A

Charges + distance between ions —> sum of forces

20
Q

Describe 3 reasons why theoretical LE is calculated

A

BH experimental data doesn’t exist
Use in BH to find (usually) less exo enthalpy of formation for unexpected compounds
Compare T + E, find validity, more than 10% difference = insufficient model, usually covalent bonding present

21
Q

Describe metallic bonding structure

A

Close packed giant lattice of positive ions and a sea of delocalised electrons
Held together by ESA between positive ions and negative electrons

22
Q

Name 3 properties of metallically bonded structures

A

High mp/bp
Malleable
Electrical conductor

23
Q

Why are metallic structures malleable

A

Same layers
Movement doesn’t change bonding

24
Q

Why are metallic structures electric conductors

A

Delocalised electrons from ions carry charge through substance

25
Why do metallic structures have high mp/bp
Giant structures Many strong bonds More ETO
26
Enthalpy change of solution
Enthalpy change for 1 mole of a substance to dissolve in water to become a solution of infinite dilution
27
Enthalpy change of hydration
Enthalpy change for 1 mole of gaseous ions to dissolve in water to become a solution of infinite dilution
28
Describe the appearance of a hydrated ion
Ion surrounded by opposite charge atoms of water molecules
29
Describe what happens when an ionic solid dissolves in water
Crystal lattice broken (endo) Water H bonds broken (endo) H point at cation O point at anion ESA (exo) Hydration
30
Describe a hydration cycle
Gaseous ions at top Aqueous ions in middle Solid lattice at bottom
31
Why is finding the enthalpy of solution from a hydration cycle unreliable (4)
- Small difference between 2 much larger values that can’t be directly found and are effected by charge and size factors - Small % uncertainty in LE of hydration enthalpy can —> large solution enthalpy % uncertainty - Solution enthalpy isn’t only solubility factor, endo solution enthalpy won’t dissolve well, large LE - Soluble compounds can form saturated solution
32
Why does poor E + T LE agreement occur
Polarisation of anion by cation Cation distorts electron cloud on anion Pulls towards shared region Nearly electron sharing Some covalent character Stronger bonding ELE more exo than TLE suggests
33
Anion and cation properties in polarisation
Cation, polarising power Anion, polarisability
34
What factors INCREASE polarising power of cation
Increase cation charge Decrease cation size Higher positive charge density = more effective distortion
35
What factors INCREASE polarisability of anion
Increase charge Increase size Larger ion = less grip on outer electrons = easier to distort
36
Name 4 levels on bonding spectrum
Pure covalent Polar covalent (unequal shared electrons) Polar ionic (distorted ions) Pure ionic
37
Name 3 allotropes of carbon
Diamond Graphite Graphene
38
Graphite 4 properties 2 uses
- Conductor, delocalised electrons between layers - Sheet formation - Each C bonded to 3 others - Soft, layers can slide Uses, electrics, pencils
39
Diamond 7 properties
- All Cs cov bonded to 4 others - Tetrahedral structure - High mp, lots ETO, many bonds - Hard, strong bonds, lattice arrangement - Thermal conductor, vibrations travel through stiff lattice - Insoluble, more attracted to neighbouring atoms that solvent molecules, no ions - Not electrical conductor, no free electrons/ions
40
Graphene 6 properties
One sheet of graphite, joined by 2 hexagons 2D, one atom thick Conductor, delocalised electrons Strong Transparent Light