Promos Flashcards

1
Q

Formula for deflection

A
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2
Q

Definition of orbital

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3
Q

How to draw s, p, and d orbitals

A
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4
Q

Exceptions to Aufbau’s Principle

A
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5
Q

Factors affecting IE

A
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6
Q

General trend across a period + exceptions

A
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7
Q

General trend down a group

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8
Q

General trend of successive IE

A
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9
Q

Definition of Metallic, Covalent and Ionic bonds

A
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10
Q

Factors affecting metallic bonds

A
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11
Q

Arrangement of ions in ionic lattice

A
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12
Q

Factors affecting ionic bond.

A
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13
Q

How to atoms in Period 3 or higher accommodate more than 8 valence electrons

A
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14
Q

Sigma vs Pi bonds, and which is stronger

A
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15
Q

Factors affecting covalent bond

A
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16
Q

Description of Silicon (IV) Oxide and Diamond

A

Diamond has a giant covalent (lattice) structure as it has a tetrahedral arrangement of atoms extensively held together by strong electrostatic forces of attraction b/w nuclei of each carbon atom and its shared electron pair.

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17
Q

Description of Graphite

A

Each carbon atom in the layer is bonded to three other carbon atoms via strong covalent bonds, forming a hexagonal arrangement of carbon atoms. The fourth valence electron of each carbon atom is delocalised in b/w the layers. Layers are held together by weak id-id forces.

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18
Q

VSEPR Theory BP-LP

A
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19
Q

Effect of electronegativities of central/non-central atoms on bond angle

A
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20
Q

Factors affecting pd-pd

A
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21
Q

How id-id interactions come about

A

At any moment in time, due to electrons continuously moving, there is a temporary distortion in the electron cloud of the molecule, giving rise to an instantaneous dipole in the molecule. This then induces a dipole in the neighboring molecule. Thus molecules are held together by the id-id interactions b/w them.

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22
Q

Factors affecting id-id

A
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23
Q

Definition of Hydrogen bonds and factor affecting its strength (know how to draw H bonds)

A
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24
Q

Ionic molecules with covalent character formation

A

Cation has high charge density, highly polarising
Anion has large electron cloud, highly polarizable
Distortion of electron cloud of anion, electron density may be shared between anion and cation, thus giving the molecule covalent character. Extent to sharing of electrons equal to extent of covalent character.

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25
How does solubility work
Energy released from forming favourable interactions b/w solute and solvent molecules is able to compensate for energy needed to overcome existing interactions b/w solute particles
26
Definition of Ion-Dipole interactions
Electrostatic forces of attraction between charged ions in a ionic compound and oppositely charged dipoles of polar molecules in solvent.
27
Solubility of giant and simple covalent structures
28
Assumptions of Ideal Gas (three)
Size of gas particles is negligible compared to size of the container Negligible intermolecular forces exerted by gas particles on one another Average kinetic energy of gas particles is directly proportional to absolute temperature
29
Daltons Law of partial pressure
The total pressure in a mixture of non reacting gases is the sum of partial pressures exerted by the constituent gases.
30
Factors affecting deviation from Ideal gas behavior (four)
31
(Optional) Definition of enthalpy change of atomisation
Enthalpy change when one mole of gaseous atoms is formed from the element in its standard state under standard conditions
32
(optional) Definition of enthalpy change of formation
Enthalpy change when one mole of substance is formed from its constituent elements in their standard states under standard conditions
33
(optional) Enthalpy change of combustion
Enthalpy change when one mole of a substance is completely burnt in oxygen under standard conditions
34
(optional) IE definition
Enthalpy change when one mole of electrons is removed from one mole of gaseous atom/singly charged cation
35
(optional) EA definition
Enthalpy change when one mole of gaseous atom/singly charged anion accepts one mole of electrons
36
Why is first EA is negative and second EA is positive
- Attraction of electron = negative EA Energy is needed to overcome repulsion b/w anion and electron to be added as both are negative.
37
(optional) BE
Average enthalpy change when one mole of covalent bonds between atoms of gaseous molecules is broken
38
(optional) H of neutralization
Enthalpy change when one mole of water is formed from the reaction of an acid and alkali under standard conditions
39
(optional) H of hydration
Enthalpy change when one mole of gaseous ions is hydrated under standard conditions
40
(optional) H of solution
Enthalpy change when one mole of a substance is completely dissolved to give an infinitely dilute solution under SC, such that there is no further enthalpy change when more solvent is added.
41
Formula for H of solution
42
Why spontaneous reaction does not mean reaction will actually take
Might not be kinetically favorable as there could be a very high Ea that prevents reaction from proceeding at a reasonable rate.
43
Definition of dynamic eqm
44
LCP
45
Effect of change in conc, pressure (volume), temperature, catalyst
46
Factors affecting ROR (know how to draw maxwell curve)
47
Definition of catalyst
48
Characteristics of catalyst (three)
49
Mode of action of heterogeneous catalyst
50
Common Ion effect
Due to a common ion in the solution, POE shift left and backward rxn is favored, thus reducing the solubility of the salt (sparingly soluble)
51
Complex Ion effect
Due to addition of a complex ion that reacts with a product of the reaction, the conc of the product decreases, thus IP
52
Conditions for enantiomers to form and definition
53
Enantiomer pair and how it affects plane polarised light
54
Idea of stability of a radical/carbocation
55
Why is trans-isomer more stable than cis-isomer
56
Why cis-isomer has higher bp than trans-isomer
57
Why cis-isomer has lower mp than trans-isomer
Cis-isomer has lower symmetry, does not pack as well into a crystalline solid compared to trans-isomer. As a result, there is less extensive intermolecular forces and thus less energy is needed to melt the solid.
58
Name of the four main reactions
59
Reagent and conditions for each sub-reaction
excess conc h2so4, heat ethanolic naoh, heat under reflux Ni catalyst, heat, H2 room temp, Br2 in CCl4 H3PO4, heat at high pressure excess conc h2so4, then heat with water cold Kmno4 (aq), dilute Naoh hot KmO4 (aq) with dilute h2so4
60
Why are alkanes generally unreactive
61
Factors for similarity and differences b/w orbitals
size, shape, energy level, distance from nucleus, electrons cant be found in center at centre of orbital
62