as topics Flashcards

(44 cards)

1
Q

state meaning of term periodicity

A

repeating patterns of physical/chemical properties going across periods

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2
Q

why does K have largest atomic radius in period 4 (2)

A
  • smallest no of protons so smallest nuclear charge
  • but same number of shells so similar shielding
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3
Q

general trend for first IE across a period and why

A

increase
increasing no protons as e- added to same shell, same shielding

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4
Q

what r the anomalies to the increase in 1st IE

A
  • small drop bw Mg+Al bc Mg has outer e- in in 3s but Al has outer e- in 3p which is higher in energy so easier to remove
  • bw P+S, S’s e- is being paired w another e- in same 3p orbital - spin pair repulsion - so easier to remove 2nd e- in orbital
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5
Q

how does MP/BP change across period 3

A

Na,Mg,Al = metallic bonding = strong bonding gets stronger the more e-s there are in outer shell that get released to sea of e-s, smaller sized ion w greater +ve charge also makes bonding strong
Si = macromolecular - many strong CBs bw atoms - high energy needed to break
Cl2, S8, P4 = simple molecular - weak VdWs bw molecules - little energy needed to break them - low mp+bp} more e- = stronger VdWs bw molecules - higher MP/BP
Ar = monoatomic - weak VdWs

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6
Q

trend in AR down grp 2

A

Atomic radius increases down the group.
As one goes down the group, the atoms have more shells of electrons making the atom bigger.

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7
Q

trend in MP down grp 2

A

Melting points decrease down the group. The metallic bonding weakens as the atomic size increases. The distance between the positive ions and delocalized electrons increases. Therefore the electrostatic attractive forces between the positive ions and the delocalized electrons weaken.

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8
Q

trend in 1st IE down grp 2

A

The outermost electrons are held more weakly because they are successively further from the nucleus in additional shells.
In addition, the outer shell electrons become more shielded from the attraction of the nucleus by the repulsive force of inner shell electrons.

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9
Q

how does Mg react w O

A

Mg burns with a bright white flame. The MgO appears as a white powder.
2 Mg + O2  2 MgO

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10
Q

what does Mg ribbon have on it and why does it have to be removed

A

Magnesium ribbon will often have a thin layer of magnesium oxide on it formed by the reaction with oxygen in the air.
2 Mg + O2  2 MgO
The magnesium oxide needs to be removed by emery paper before doing reactions with magnesium ribbon.
If testing for reaction rates with Mg and acid, an un-cleaned Mg ribbon would give a false result because both the Mg and MgO would react but at different rates.
Mg + 2 HClMgCl2 + H2
MgO + 2 HClMgCl2 + H2O

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11
Q

how does Mg react in steam

A

Magnesium reacts in steam to produce magnesium oxide and hydrogen. The Mg would burn with a bright white flame. The MgO appears as a white powder.
Mg(s) + H2O(g)  MgO(s) + H2(g)

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12
Q

how does Mg react in warm water

A

Mg will also react with warm water, giving a different magnesium hydroxide product.
Mg + 2 H2OMg(OH)2 + H2
This is a much slower reaction than the reaction with steam and there is no flame.

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13
Q

how do other grp 2 metals react w cold water

A

fizzing, (more vigorous down group)
the metal dissolving, (faster down group) the solution heating up (more down group)
with calcium a white precipitate appearing (less precipitate forms down group with other metals)

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14
Q

why is Ti useful and whats it used for

A

because it is abundant, has a low density and is corrosion resistant – it is used for making strong, light alloys for use in aircraft.

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15
Q

why can Ti not be extracted w carbon or by electrolysis

A

Titanium cannot be extracted with carbon because titanium carbide (TiC) it is formed rather than titanium.
Titanium cannot be extracted by electrolysis because it has to be very pure

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16
Q

Steps in extracting titanium

A
  1. TiO2 (solid) is converted to TiCl4 (liquid) at 900C:
    TiO2 +2Cl2 +2CTiCl4 +2CO
  2. The TiCl4 is purified by fractional distillation in an argon atmosphere.
  3. The Ti is extracted by Mg in an argon atmosphere at 500C:
    TiCl4 + 2Mg  Ti + 2 MgCl2
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17
Q

Titanium is expensive because: 4

A

The expensive cost of the magnesium
2. This is a batch process which makes it expensive because the process is slower (having to fill up and empty reactors takes time) and requires more labour and the energy is lost when the reactor is cooled down after stopping
3. The process is also expensive due to the argon, and the need to remove moisture (because TiCl4 is susceptible to hydrolysis).
4. High temperatures required in both steps

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18
Q

why tio2 converted ticl4

A

TiO2 is converted to TiCl4 as it can be purified by fractional distillation, TiCl4 being molecular (liquid at room temperature) rather than ionic like TiO2 (solid at room temperature).

19
Q

what is CaO used for

A

Calcium oxide can be used to remove SO2 from the waste gases from furnaces (e.g. coal fired power stations) by flue gas desulfurisation. The gases pass through a scrubber containing basic calcium oxide which reacts with the acidic sulfur dioxide in a neutralisation reaction.
SO2 + CaOCaSO3 calcium sulfite
The calcium sulfite which is formed can be used to make calcium sulfate for plasterboard.

20
Q

what do grp 2 hydroxides appear as

A

white precipitates

21
Q

Magnesium hydroxide is used .. and why

A

in medicine (in suspension as milk of magnesia) to neutralise excess acid in the stomach and to treat constipation.
Mg(OH)2 + 2HClMgCl2 + 2H2O
It is safe to use because it is so weakly alkaline. It is preferable to using calcium carbonate as it will not produce carbon dioxide gas.

22
Q

Ca(OH)2 use

A

to neutralise acidic soils. test for carbon dioxide. The limewater turns cloudy as white calcium carbonate is produced.
Ca(OH)2 (aq) + CO2 (g)  CaCO3 (s) + H2O(l)

23
Q

BaSO4 is used .. why

A

in medicine as a ‘Barium meal’ given to patients who need x-rays of their intestines. The barium absorbs the x-rays and so the gut shows up on the x-ray image. Even though barium compounds are toxic, it is safe to use here because barium sulfate’s low solubility means it is not absorbed into the blood.

24
Q

how to test for presence of sulphate ion

A

BaCl2 solution acidified with hydrochloric acid is used as a reagent to
test for sulfate ions.
If acidified barium chloride is added to a solution that contains sulfate ions a
white precipitate of barium sulfate forms.

25
why is Hal needed in sulphate ion test
The hydrochloric acid is needed to react with carbonate impurities that are often found in salts which would form a white barium carbonate precipitate and so give a false result. You could not use sulfuric acid because it contains sulfate ions and so would give a false positive result. 2HCl + Na2CO3  2NaCl + H2O + CO2 Fizzing due to CO2 would be observed if a carbonate was present.
26
when to use vacuum filtration? what is it
Use if larger amounts of solid are formed. The apparatus is connected to a water pump which will produce a vacuum. Buchner funnel Buchner flask (has thicker glass walls than a normal flask to cope with the vacuum )Filter paper, Air outlet to water pump
27
how does fluorine appear
v pale yellow gas
28
cl appearance
greenish gas
29
br appearance
red liquid, gives off dense brown/orange fumes
30
iodine appearance
shiny grey solid - sublimes to purple gas
31
trend in MP/BP down grp 7
Increase down the group As the molecules become larger they have more electrons and so have larger van der waals forces between the molecules. As the intermolecular forces get larger more energy has to be put into break the forces. This increases the melting and boiling points.
32
trend n electronegativity in grp 7
Electronegativity is the relative tendency of an atom in a molecule to attract electrons in a covalent bond to itself. As one goes down the group the electronegativity of the elements decreases. As one goes down the group the atomic radii increases due to the increasing number of shells. The nucleus is therefore less able to attract the bonding pair of electrons.
33
does oxidising strength decrease/increase down grp 7
DECREASE
34
cl/br/I colour in soln
cl = v pale green soln br = yellow soln I = brown soln
35
why is nitric acid added when identifying halides
to react with any carbonates present to prevent formation of the precipitate Ag2CO3. This would mask the desired observations 2 HNO3 + Na2CO3 2 NaNO3 + H2O + CO2
36
does reducing strength decrease/increase down grp 7, why
INCREASE A reducing agent donates electrons. The reducing power of the halides increases down group 7 They have a greater tendency to donate electrons. This is because as the ions get bigger it is easier for the outer electrons to be given away as the pull from the nucleus on them becomes smaller.
37
how do F- + Cl- react w H2So4
F- and Cl- ions are not strong enough reducing agents to reduce the S in H2SO4. No redox reactions occur. Only acid-base reactions occur. NaF(s) + H2SO4(l)NaHSO4(s) + HF(g) Observations: White steamy fumes of HF are evolved. NaCl(s) + H2SO4(l)NaHSO4(s) + HCl(g) Observations: White steamy fumes of HCl are evolved. These are acid – base reactions and notredoxreactions.H2SO4 playsthe role of an acid (proton donor).
38
br- + H2SO4, reaction equations, REDOX equations, observations, sulfuric acid role
Br- ions are stronger reducing agents than Cl- and F- and after the initial acid-base reaction, the bromide ions reduce the sulfur in H2SO4 from +6 to + 4 in SO2 Overall equation: combining two steps above: 2NaBr + 3H2SO4  2NaHSO4 + SO2 + Br2 + 2H2O Acid- base step: NaBr(s) + H2SO4(l)  NaHSO4(s) + HBr(g) Redox step: 2 H+ + 2 Br - + H2SO4 Br2(g) + SO2(g) + 2 H2O(l) Observations: White steamy fumes of HBr are evolved. orange fumes of bromine are also evolved and a colourless, acidic gas SO2 Ox 1⁄2 equation 2Br -Br2 + 2e- Re1⁄2equationH2SO4 +2H+ +2e-  SO2 +2H2O Note the H2SO4 plays the role of acid in the first step producing HBr and then acts as an oxidising agent in the second redox step.
39
I- + h2so4
I- ions are the strongest halide reducing agents. They can reduce the sulfur from +6inH2SO4 to+4inSO2,to 0 in S and -2 in H2S. Observations: White steamy fumes of HI are evolved. Black solid and purple fumes of Iodine are also evolved A colourless, acidic gas SO2 A yellow solid of sulfur H2S (Hydrogen sulfide), a gas with a bad egg smell, NaI(s) + H2SO4(l)NaHSO4(s) + HI(g) 2 H+ + 2 I- + H2SO4I2(s) + SO2(g) + 2 H2O(l) 6H+ +6I- +H2SO4 3I2 +S(s)+4H2O(l) 8H+ +8I- +H2SO44I2(s) + H2S(g) + 4H2O(l) Ox 1⁄2 equation 2I -  I2 + 2e- Re1⁄2equationH2SO4 +2H+ +2e-  SO2 +2H2O Re1⁄2equationH2SO4 +6H+ +6e-  S+4H2O Re1⁄2equationH2SO4 +8H+ +8e-  H2S+4H2O Reduction products = sulfur dioxide, sulfur and hydrogen sulfide Note the H2SO4 plays the role of acid in the first step producing HI and then acts as an oxidising agent in the three redox steps.
40
chlorine w water reaction
Cl2(g) + H2O(l)⇌ HClO(aq) + HCl(aq)
41
what happens if cl bubbled thru water in sunlight, observation
2Cl2 + 2H2O4H+ + 4Cl- + O2 The greenish colour of chlorine water fades as the Cl2 reacts and a colourless gas (O2) is produced.
42
what happens if UI added to reaction mixture of Cl2 + h20
If some universal indicator is added to the solution it will first turn red due to the acidity of both reaction products. It will then turn colourless as the HClO bleaches the colour.
43
what is chlorine used for
water treatment to kill bacteria. It has been used to treat drinking water and the water in swimming pools. The benefits to health of water treatment by chlorine outweigh its toxic effects.
44
Reaction of chlorine with cold dilute NaOH solution, observation
Cl2,(and Br2, I2) in aqueous solutions will react with cold sodium hydroxide. The colour of the halogen solution will fade to colourless. Cl2 (aq) + 2 NaOH (aq)  NaCl (aq) + NaClO (aq) + H2O (l) The mixture of NaCl and NaClO is used as bleach and to disinfect/ kill bacteria.