Module 3 Periodicity Flashcards

(55 cards)

1
Q

D block

A

The part of the periodic table in which the element have their highest energy electron in the d orbital

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2
Q

p-block

A

the part of the periodic table in which the elements have their highest energy
electron in a p-orbital

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3
Q

s-block

A

the part of the periodic table in which the elements have their highest energy
electron in an s-orbital

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4
Q

First ionisation energy

A

The removal of one mole of electrons from one mole of gaseous atoms. Factors which affect the first ionisation energy are: the strength of attraction between the electron and the nucleus, the nuclear charge and the atomic radius. There is a small decrease in first ionisation energy due to s- and p-subshell energies (between Be and B) and p-orbital repulsion.

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5
Q

Electron configuration

A

The arrangement of electrons into orbitals and energy levels around the nucleus of an atom.

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6
Q

Giant covalent lattice

A

A network of atoms connected by strong covalent bond. Giant covalent lattices typically insoluble with a high melting and boiling point due to the presence of strong covalent bonds. They are also poor electrical conductors as they don’t contain mobile charges particles.

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7
Q

Metallic Bonding

A

strong electrostatic attraction between cations and delocalised electrons.

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8
Q

Giant Metallic Lattice Structure

A

the structure of all metals, made up of cations and delocalised electrons. Giant metallic structures are typically insoluble with a high melting and boiling points due to strong electrostatic forces of attraction between cations and electrons.
Metals are good electrical conductors due to the presence of delocalised electrons.

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9
Q

Periodicity

A

a repeating trend in physical and chemical properties across the periods of the
periodic table

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10
Q

Successive Ionisation Energies

A

the energy required to remove each electron one-by-one
from one mole of gaseous atoms / ions

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11
Q

Electron Configuration

A

the arrangement of electrons into orbitals and energy levels around
the nucleus of an atom/ ion. Group 2 elements have an s2
outer shell electron configuration

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12
Q

First Ionisation Energy

A

the removal of one mole of electrons from one mole of gaseous
atoms. Factors which affect the first ionisation energy are: the strength of attraction between the electron and the nucleus, the nuclear charge and the atomic radius.

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13
Q

Group 2 Oxide

A

a compound with the general formula MO, where M is a group 2 element.
When group 2 oxides react with water, they form an alkaline solution, with alkalinity increasing down the group.

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14
Q

Second Ionisation Energy

A

the removal of one mole of electrons from one mole of gaseous
1+ ions to form one mole of 2+ ions

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15
Q

Boiling Point

A

the temperature at which a liquid boils and becomes a gas. Boiling point
increases down group 7 due to the increasing strength of London Forces between the halogen molecules

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16
Q

Diatomic Molecules

A

molecules that are made up of 2 atoms. Halogens are diatomic

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17
Q

Displacement Reaction

A

a reaction in which one atom is replaced by another. Halogens can
undergo displacement reactions as their reactivity decreases down the group. The more reactive halogen will displace the less reactive halogen from a solution of its salt.

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18
Q

Disproportionation

A

the oxidation and reduction of the same element. Examples include the
water treatment (reacting chlorine with water) and bleach formation (reacting chlorine with cold, dilute aqueous sodium hydroxide)

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19
Q

Precipitation Reaction:

A

a reaction in which two aqueous solutions are combined to form an
insoluble salt (a precipitate). Halide anions undergo precipitation reactions with aqueous silver ions

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20
Q

Water Treatment

A

the addition of chlorine to water to kill bacteria. The risks associated with
the use of chlorine to treat water are the hazards of toxic chlorine gas and the possible risks from the formation of chlorinated hydrocarbons

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21
Q

Carbonate

A

a salt containing the CO3 2- anion. A reaction between a carbonate and H+ will form CO2

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22
Q

Ammonium Ion

A

an ion with the formula NH4+ The test for ammonium ions is a reaction with warm NaOH, which forms NH3

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23
Q

halides

A

a salt containing a group 7 anion. Cl-, Br-and I- can be tested for using a solution of
silver ions as this reaction forms a coloured precipitate. The solubility of the precipitate is then tested using dilute and concentrated ammonia

24
Q

Qualitative Analysis

A

identifies the elements present in a substance, typically using
test-tube reactions

25
Sulfate
a salt containing the anion SO4 2-. A reaction between SO4 2- and Ba2+(aq) will form a precipitate
26
Activation Energy
the minimum energy required for a reaction to take place.
27
Average Bond Enthalpy
the energy required to break one mole of gaseous bonds. Actual bond enthalpies may differ from the average as the average bond enthalpy considers a particular bond in a range of molecules
28
Endothermic
a reaction which takes in energy (ΔH is positive). More energy is required to break bonds than is released by making bonds.
29
Exothermic
a reaction which gives out energy (ΔH is negative). More energy is released by bond making than is used in bond breaking
30
Enthalpy (H)
a value that represents the heat content of a system.
31
Enthalpy Change (ΔH)
the change in the heat content of a system during a reaction. This can be determined from experimental results using q = mcΔT (where q is the heat change of the surroundings, m is the mass of the surroundings, c is the specific heat capacity and ΔT is the change in temperature) ΔH=q/mols
32
Enthalpy Change of Combustion (ΔcH)
the enthalpy change that takes place when one mole of a substance is completely combusted
33
Enthalpy Change of Formation (ΔfH)
the enthalpy change that takes place when one mole of a compound is formed from its elements.
34
Enthalpy Change of Neutralisation (ΔneutH)
the enthalpy change that takes place when one mole of water is formed from a neutralisation reaction
35
Enthalpy Change of Reaction (ΔrH)
the enthalpy change that is associated with a particular chemical equation.
36
Enthalpy Profile Diagram
shows the difference in the enthalpy of reactants and products as well as the activation energy of a reaction.
37
Hess’ Law
the enthalpy change of a reaction is independent of the route it takes.
38
Standard Conditions
a pressure of 100 kPa and a temperature of 298K
39
Standard State
the physical state (s, l, g, aq) of a substance under standard conditions
40
Boltzmann Distribution
a graph showing the distribution of the energies of molecules in relation to the activation energy. Increasing temperature will increase the proportion of molecules with energy above the activation energy. A catalyst lowers the activation energy meaning more molecules will have sufficient energy to reac
41
Catalyst
a substance that speeds up the rate of a reaction without being used up. A catalyst allows the reaction to proceed via a different route with a lower activation energy. Catalysts are important in terms of economics and sustainability as they enable processes to take place at lower temperatures meaning less energy is required
42
Collision Theory
the theory which states that molecules must collide with sufficient energy at the correct orientation for a reaction to occur.
43
Concentration
the amount of a substance that is dissolved per unit volume of solution. Increasing the concentration increases the rate of reaction as there are more molecules in the same volume meaning more frequent successful collisions
44
Enthalpy Profile Diagram
shows the difference in the enthalpy of reactants and products as well as the activation energy of a reaction
45
Heterogeneous Catalyst
a catalyst that is in a different state to the reactants (e.g. a solid catalyst with gaseous reactants)
46
Homogeneous catalyst
a catalyst which is in the same state as the reactants
47
Pressure
the force that a gas exerts on the walls of a container. Increasing the pressure increases the rate of reaction as there are more molecules in the same volume (or the same number of molecules in a smaller volume) meaning more frequent successful collisions.
48
Rate of Reaction
a measure of how quickly a reactant is used up/ a product is formed. Rate can be determined by measuring concentration, the volume of gas produced or the mass lost over time
49
Compromise
balancing several different factors in order to get the best possible outcome. In industry, the position of the equilibrium and rate of reaction must be considered when deciding the conditions for the reaction. These factors must also be balanced with safety and economics.
50
Dynamic Equilibrium:
a closed system in which the rates of the forward and reverse reactions are equivalent. The concentrations of reactants and products don’t change.
51
Homogeneous Equilibrium
an equilibrium in which all reactants are in the same state.
52
Le Chatelier’s Principle
when a system in dynamic equilibrium is subject to change, the position of equilibrium will shift to minimise the change. This principle is used to determine the effect of changing pressure, temperature or concentration on the position of equilibrium.
53
KC
the equilibrium constant that is equal to the concentration of products raised to their stoichiometric coefficients divided by the concentration of reactants to the power of their stoichiometric coefficients. When KC is greater than 1, the equilibrium favours the products. When KC is less than 1, the equilibrium favours the reactants
54
Enthalpy of formation equation
Reaction energy= (sum of)products - (sum of)reactants
55
Enthalpy of combustion equation
Reaction energy=(sum of) reactants - (sum of) products