Chapter 8 Flashcards

1
Q

Why are s2 metals so reactive? ( Group 2 )

A

Loss of 2 electrons from the atom produces a 2+ ion with noble gas electronic configuration.

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2
Q

How do s2 metals form ionic compounds ?

A

Through loss of their s2 electrons in redox reactions, forming 2+ ions

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3
Q

How do Group 2 metals react with water ?

A

They react with water to form alkaline hydroxides + hydrogen - general formula m(OH)2.
The metal is oxidised and Hydrogen is reduced

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4
Q

How do Group 2 metal oxides react with water ?

A

Only produce metal hydroxide

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5
Q

How do Group 2 metals react with oxygen ?

A

They react with oxygen to form metal oxides with general formula MO. Metal is oxidised, Oxygen is reduced

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6
Q

How do Group 2 metals react with dilute acids?

A

They react with dilute acids to form a salt + hydrogen.
Metal is oxidised and Hydrogen is reduced

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7
Q

What happens to the reactions with water, oxygen and dilute acids as you go down Group 2 ?

A

The reaction becomes more vigorous as reactivity increases

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8
Q

Can you explain the trend in reactivity in terms of the first and second ionisation energies of Group 2 elements down the group?

A

Reactivity increases down Group 2 - s2 electrons are lost more easily ( less energy required )
Reactivity is reflected in ionisation energy, which decreases down the group.
The atomic radius increases and the outer electrons are more shielded, and so bonding electrons are less strongly attracted to the nucleus.
The atomic radius increases and there are more filled energy levels between the nucleus and the outer electron, and more shielding means lower I.E.

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9
Q

What is produced when Group 2 oxides react with water ?

A

Hydroxide ( precipitate usually )

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10
Q

Can group 2 hydroxides dissolve in water ?

A

If there is lots of water, then the hydroxides will dissolve, but Group 2 hydroxides are only slightly soluble in water. This means that they will be precipitated from solution if concentrations of the metal and OH- ions are high.

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11
Q

Why are the Group 2 hydroxides produced referred to as alkali hydroxides ?

A

They are soluble bases that produce OH- ions in water

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12
Q

What does the pH of the Group 2 hydroxides depend on ?

A

pH depends on how much OH- in in solution. Higher pH = more OH- ions.

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13
Q

What happens to the strength, solubility and alkalinity of bases ( Group 2 ) as you go down the group ?

A

Strength increases as you down the group
Solubility increases as you go down the group
More soluble = more OH- ions = more alkaline ( more concentrated solution )

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14
Q

What is the trend in solubility of Group 2 hydroxides ?

A

The solubility of the hydroxides increases down the group.
More concentrated solutions are more alkaline

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15
Q

Describe uses of some Group 2 compounds as bases, including equations ( eg Ca(OH)2 )

A

Oxides, carbonates and hydroxides are bases. Group 2 bases have uses related to the fact that they can neutralise acids.
CaO + HCl →CaCl2 + H20
Ca(OH)2 + H2SO4 →CaSO4 + 2H20
CaCO3 + 2HNO3 →Ca(NO3)2 + H20 + CO2

hydroxide eg Ca(OH)2 is used in agriculture - added to fields by farmers to raise the pH of acid soil :
Ca(OH)2(s) + 2H+(aq) →Ca2+(aq) + 2H2O(l)

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16
Q

Describe uses of some Group 2 compounds as bases, including equations, for example Mg(OH)2 and CaCO3 as ‘antacids’ in treating indigestion

A

Group 2 bases are used to treat acid indigestion (antacid).
Mainly magnesium hydroxide and calcium carbonate are used.
Stomach acid is mainly HCl(aq).
Mg(OH)2 is used as a suspension in water because the solubility of magnesium hydroxide is low.

Mg(OH)2 + 2HCl(aq) → MgCl2(aq) + 2H2O(l)
CaCO3(s) + 2HCl(aq) → CaCl2(aq) + H2O(l) + CO2(g)

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17
Q

Explain the existence of halogens as diatomic molecules

A

Each halogen is short of one electron to complete its octet and hence, has a strong tendency to share its unpaired electron with another atom of the same halogen to form diatomic molecules.

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18
Q

What colour and state are F, Cl, Br and I at room temp ?

A

F = yellow gas
Cl = green gas
Br = dark red brown liquid
I = dark grey solid that turns purple after heating

19
Q

Explain the trend in the boiling points of Cl2, Br2 and I2, in terms of induced dipole–dipole interactions (London forces)?

A

Boiling / melting point increases going down the group
More electrons
Greater fluctuations in electronegativity
More / greater induced dipoles present
Greater London forces between molecules
More energy required to break London forces

20
Q

How do halogens form a 1- ions ?

A

the initial outer shell s2p5 electron configuration and the gaining of one electron in many redox reactions

21
Q

When are ionic and covalent compounds produced with halogens ?

A

Halogens give ionic compounds with metals (NaCl) but covalent compounds with non-metals (NCl3).

22
Q

Explain the trend in reactivity of the halogens Cl2, Br2, and I2, illustrated by reaction with other halide ions?

A

A more reactive halogen will displace the less reactive halogen in solution. ( displacement reactions )
Halide ions are oxidised to the elemental halogen and the halogen is reduced to the halide ion.
In interhalogen compounds the more reactive halogen will be in the -1 oxidation state (the other will be in a positive oxidation state).

23
Q

Are the halogens soluble in water and why ?

A

They are poorly soluble in water. There is little attraction between halogen molecules and water molecules. The inter molecular bonding between polar heads in water are too strong to be broken

24
Q

What colours are chlorine, bromine and iodine in water ?

A

Chlorine = pale green
Bromine = orange
Iodine = brown ( iodine ions are colourless )

25
Q

Are the halogens soluble in non polar, organic solvents ( eg cyclohexane ) and why ?

A

They are quite soluble because the intermolecular forces can form between the halogen molecules and the solvent. Due to their greater solubility, solutions of the halogens in non-polar solvents are much
darker than in water

26
Q

What colours are chlorine, bromine and iodine in organic solvents ?

A

Chlorine = pale green
Bromine = orange
Iodine = violet ( iodine ions are colourless )

27
Q

Explain the trend in reactivity from the decreasing ease of forming 1– ions, in terms of attraction, atomic radius and electron shielding?

A

Increasing atomic radius
Increased shielding from inner shells
Less nuclear attraction to capture an electron from another species
Reactivity decreases down the group

28
Q

Why are the halogens described as powerful oxidising agents ?

A

Because they are electron acceptors

29
Q

Put F2, Br2, I2 and Cl2 in order of increasing oxidising power

A

F2 > Cl2 > Br2 > I2

30
Q

Put F2, Br2, I2 and Cl2 in order of increasing reducing power

A

I2 > Br2 > Cl2 > F2

31
Q

Explain the term disproportionation, illustrated by the reaction of chlorine with water as used in water purification?

A

oxidation and reduction of the same element
Cl2 (g) + H2O (l)—-> HClO(aq) + HCL(aq)

32
Q

Explain the term disproportionation as oxidation and reduction of the same element, illustrated by the reaction of chlorine with cold, dilute aqueous sodium hydroxide, as used to form bleach?

A

Cl₂ (g) + 2NaOH (aq) → NaCl (aq) + NaClO (aq) + H₂O (l)

33
Q

List and describe the benefits of chlorine use in water treatment contrasted with associated risks?

A

Pros : without chlorine in our water, we would be at risk of diseases such as typhoid and cholera.
Cons : Chlorine is a toxic gas.
Chlorine will react with methane in water (along with other organic hydrocarbons). Methane is formed by decaying vegetation.
The result of these reactions are chlorinated hydrocarbons, which are suspected carcinogens

34
Q

How to test for halide ions ?

A

Add silver nitrate to sample
Observe colour of precipitate

35
Q

What happens in the reaction between aq silver ions ( in the form of silver nitrate ) and aqueous Cl - ions ?

A

White precipitate forms
Ag+ (aq) + Cl-(aq) 🡪AgCl(s) (white precipitate)

36
Q

What happens in the reaction between aq silver ions ( in the form of silver nitrate ) and aqueous Br - ions ?

A

Cream precipitate forms
Ag+ (aq) + Br-(aq) 🡪AgBr(s) (cream precipitate)

37
Q

What happens in the reaction between aq silver ions ( in the form of silver nitrate ) and aqueous I - ions ?

A

Yellow precipitate forms
Ag+ (aq) + I-(aq) 🡪 AgI(s) (yellow precipitate)

38
Q

How do you distinguish between the silver halide precipitates ( of chlorine, bromine and iodine )formed after adding silver nitrate to the samples ?

A

Add aqueous ammonia solution

Dilute ammonia solution dissolves the white chloride precipitate but no others.
Concentrated ammonia dissolves the cream bromide and white chloride.
The yellow iodide precipitate does not dissolve in any ammonia solutions.

39
Q

What colour are halide, carbonate, sulphate and ammonium ions in solution ?

A

Colourless

40
Q

How to test for carbonate ions

A

Add acid ( nitric acid ) to produce a salt, water and carbon dioxide gas. The CO2 gas shows the presence of carbonate ions

41
Q

How to test for sulphate ions

A

Add barium ions ( Ba2+ ) in the form of Barium nitrate to sample. White precipitate is formed and CO2 gas. Barium sulphate is insoluble in water ( precipitate )

42
Q

How to test for ammonium ions

A

Hear sample with warm aq sodium hydroxide to form ammonia gas (NH3). Ammonia is alkaline so can be tested - turns damp litmus paper blue as ammonia dissolves in water.

43
Q

In what order should carbonates ions, sulphate ions and halide ions be tested ?

A

1) Carbonate
2) Sulphate
3) Halide

44
Q

Why should you carry out ion tests in a specific order ?

A

The first test is unequivocal and is not affected by any sulphate or halide ions present.
The halide test is carried out last because if there is any CO32- and SO42- present, precipitates of Ag2CO3 and Ag2SO4 would be formed – so these ions need to be removed in the first two tests).
If you plan to test for sulphate and halide ions you must make sure that these are not
part of the reagents used for the tests.
So for the carbonate test, the acid must not be hydrochloric acid or sulphuric (VI) acid.
So use nitric (V) acid for the carbonate test. Similarly, you should not use BaCl2 for the sulphate test as this will introduce Cl- ions that will spoil the halide test.
So use barium nitrate solution for the sulphate test.
After the sulphate test, the solution may need to be filtered before doing the halide test. This will make seeing any further precipitate straightforward.