as topics Flashcards
(44 cards)
state meaning of term periodicity
repeating patterns of physical/chemical properties going across periods
why does K have largest atomic radius in period 4 (2)
- smallest no of protons so smallest nuclear charge
- but same number of shells so similar shielding
general trend for first IE across a period and why
increase
increasing no protons as e- added to same shell, same shielding
what r the anomalies to the increase in 1st IE
- 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
how does MP/BP change across period 3
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
trend in AR down grp 2
Atomic radius increases down the group.
As one goes down the group, the atoms have more shells of electrons making the atom bigger.
trend in MP down grp 2
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.
trend in 1st IE down grp 2
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.
how does Mg react w O
Mg burns with a bright white flame. The MgO appears as a white powder.
2 Mg + O2 2 MgO
what does Mg ribbon have on it and why does it have to be removed
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 HClMgCl2 + H2
MgO + 2 HClMgCl2 + H2O
how does Mg react in steam
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)
how does Mg react in warm water
Mg will also react with warm water, giving a different magnesium hydroxide product.
Mg + 2 H2OMg(OH)2 + H2
This is a much slower reaction than the reaction with steam and there is no flame.
how do other grp 2 metals react w cold water
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)
why is Ti useful and whats it used for
because it is abundant, has a low density and is corrosion resistant – it is used for making strong, light alloys for use in aircraft.
why can Ti not be extracted w carbon or by electrolysis
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
Steps in extracting titanium
- TiO2 (solid) is converted to TiCl4 (liquid) at 900C:
TiO2 +2Cl2 +2CTiCl4 +2CO - The TiCl4 is purified by fractional distillation in an argon atmosphere.
- The Ti is extracted by Mg in an argon atmosphere at 500C:
TiCl4 + 2Mg Ti + 2 MgCl2
Titanium is expensive because: 4
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
why tio2 converted ticl4
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).
what is CaO used for
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 + CaOCaSO3 calcium sulfite
The calcium sulfite which is formed can be used to make calcium sulfate for plasterboard.
what do grp 2 hydroxides appear as
white precipitates
Magnesium hydroxide is used .. and why
in medicine (in suspension as milk of magnesia) to neutralise excess acid in the stomach and to treat constipation.
Mg(OH)2 + 2HClMgCl2 + 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.
Ca(OH)2 use
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)
BaSO4 is used .. why
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.
how to test for presence of sulphate ion
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.