The periodic table Flashcards

1
Q

Periodicity

A

a regular periodic variation of properties of elements with atomic number and position in the periodic table

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2
Q

First ionisation energy-

A

energy required to remove 1 electron from each atom in 1 mole of gaseous atoms to form 1 mole of gaseous 1+ ions

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3
Q

Factors affecting ionisation energy

A

-atomic radius- larger atomic radius, the lower nuclear attraction, therefore lower ionisation energy
-nuclear charge- higher nuclear charge, larger nuclear attraction
-electron shielding- the more shells, the larger the shielding, so less nuclear attraction

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4
Q

1st, 2nd and 3rd ionisation energy equations for Li

A

Li-> e- + Li+
Li+ -> e- + Li2+
Li2+-> e- + Li3+

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5
Q

Successive ionisation energies

A

-electrons removed, less repulsion between remaining electrons, so drawn closer nucleus
-positive nuclear charger outweighs the negative charge every time an electron is removed
-as the distance of each electron to the nucleus decreases, nuclear attraction increases, causing ionisation energy to increase

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6
Q

Draw ionisation graph for nitrogen (7)

A

graph

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7
Q

Ionisation energy trend across period

A

-general increase because:
-higher nuclear charge as more protons
-electrons added to same shell, which is drawn closer to nucleus
-same number of inner shells, so no change in shielding

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8
Q

8 elements that don’t follow ionisation energy trend

A

Be-> B and Mg-> Al
-both decrease in ionisation energy even though they’re further along period
-this is because B and Al have their outer electron in a P orbital whereas Be and Mg outer electron is in an S orbital
-P orbitals have higher energy and therefore further from the nucleus
-this therefore decreases nuclear attraction, meaning lower ionisation energy
N->O P->S decrease ionisation energies even though they’re along the period
-because in N and P, each p orbital only contains one electron
-in O and S, the p orbital has 2 electron in = spin paired
-spin paired electrons experience some repulsion and therefore are easier to remove

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9
Q

Ionisation energy trends down a group

A

-first ionisation energies decrease
-more shells, so more shielding
-larger atomic radius
-nuclear charge increases, but its effects are outweighed by atomic radius and shielding

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10
Q

Metallic bonding

A

electrostatic forces of attraction between positive ions and delocalised electrons

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11
Q

Giant metallic lattice structure

A

-delocalised electrons spread throughout
-electrons free to move
-over whole structure, charges balance

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12
Q

Properties of giant metallic lattices

A

-high MP and BP- attraction between ions and electrons are very strong so high temp required to overcome electrostatic forces
-electrical conductors- delocalised electrons free to move and can carry charge
-ductile- can be drawn out/ stretched eg. wires
-malleable- can be hammered into different shapes

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13
Q

Types bonding across elements in period 2 + 3

A

Giant metallic:
-Li, Be
-Na, Mg, Al
Giant covalent
-B, C
- Si
Simple molecular
-N2, O2, F2, Ne
-P4, S8, CL2, Ar

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14
Q

Trend melting points in metals

A

-across the period, MP increases
-this is because ionic charge increases, ionic size decreases
-therefore attraction between ions and electrons increase, so more energy required to disrupt the lattice

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15
Q

Group 2 properties

A

-high MP + BP
-light metals, low densities
-white compounds

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16
Q

Reaction group 2 element and O2 eg. Ca

A

2M + O2 -> 2MO
2Ca + O2 -> 2CaO

17
Q

Reaction group 2 elements and H2O eg. Ca

A

M + 2H2O -> M(OH)2 + H2
Ca + 2H2O -> Ca(OH)2 + H2

18
Q

Reaction group 2 elements and dilute acid eg. Ca + HCl

A

M + 2HCl-> MCl2 + H2
Ca + 2HCl -> CaCl2 + H2

19
Q

Group 2 oxide + H2O

A

MO + H2O -> M(OH)2
CaO + H2O -> Ca(OH)2

20
Q

Solubility of group 2 hydroxides

A

-solubility of hydroxides increase down the group
-this is because they release more OH-
-therefore alkalinity increases down the group
-Be(OH)2 = insoluble
-more soluble= less likely to form precipitate

21
Q

Uses group 2 compound

A

Ca(OH)2
- neutralise soils by reducing acidity
Mg(OH)2
-used in indigestion tablets by neutralising excess stomach acid
CaCO3
-used in limestone and marble
-drawback as it readily reacts with acid, rainwater is slightly acidic so therefore erodes over time

22
Q

Trend BP of halogens

A

-Bp increases down the group
-down group physical state changes from gas to liquid to solid (F2 + Cl2= gas, Br2= liquid, I2 + At2= solid)
-this is because each elment has an extra shell of electrons leading to stronger london forces between molecules

23
Q

Halogen REDOX reactions

A

-Cl2 can oxidise Br- and I- ions
-Br can only oxides I-

24
Q

Colour of halogen in water

A

Cl2= pale green
Br2= orange
I2= brown

25
Q

Colour of halogen in cyclohexane

A

Cl2= pale green
Br2= orange
I2= violet

26
Q

Disproportionation-

A

reaction where the same element is both oxidised and reduced
eg. Cl2 + H2O -> HClO + HCl

27
Q

Formation bleach

A

Cl2 + 2NaOH -> NaCl + NaClO + H2O

28
Q

CO3 2- test

A

-add dilute strong acid eg. H2SO4
-collect any gas and bubble through limewater
-should fizz as CO2 produced
-CO2 turns limewater cloudy

29
Q

SO4 2- test

A

-add dilute HCl and BaCl2
-white ppt

30
Q

Halide ions test

A

-dissolve suspected halide in water
-add silver nitrate
-add ammonia if can’t distinguish colour
-Cl- = white ppts, soluble in dilute NH3
-Br- = cream ppt, soluble in conc NH3
-I- = yellow ppt, insoluble in NH3

31
Q

NH4+ test

A

-add NaOH and heat gently
-test any gas with red litmus paper
-ammonia turns red litmus paper blue