Showing posts with label HSC. Show all posts
Showing posts with label HSC. Show all posts

Tuesday, 10 September 2013

9.6.3 HSC Question Feedback


2002 aii) – To reverse a galvanic cell and make it an electrolysis cell we have to reverse both the anode and cathode reactions. If we apply the exact opposite voltage produced by the galvanic cell all we do is stop the galvanic cell reaction. To reverse the cell we have to apply GREATER than the galvanic cell potential.

2003 bii) Any time you describe an experiment to measure the rate of electrolysis you MUST specify HOW you measured the rate – eg In our experiment we measured the mass change of the anode as an indication of the rate of reaction.

2006 bi) For the risk assessment and HOW it INFLUENCED our PROCEDURE– we used slightly toxic CuSO4 – this may have limited our concentration to lower (safer) concentrations. We also used a power pack that limited the voltage to 12V to minimise the risk of electrocution but this limited our experiment to less than 12 V

2006 bii) When providing a conclusion from YOUR OBSERVATIONS you have to state the observations – eg the electrolysis cell that had the higher voltage had a greater mass loss at the anode in a fixed time. Thus it was concluded that higher voltages increase rates of electrolysis.

2007 ai) Graphite rods are used because they are INERT (meaning that they wont react in the redox reactions) CONDUCTORS (this allows them to transport re electrons required for electrolysis) – a lot of people forgot to mention that they are conductors. GRAPHITE IS NOT A METAL!

2008 ciii) It did say “Identify” the factors that affect rates of electrolysis but which of these two answers (that take basically the same time) is going to score more highly?:

·        Voltage, electrode spacing, electrode size and electrolyte concentration all affect electrolysis rates

OR

·        ­ voltage, ¯ electrode spacing, ­ electrode size and ­ electrolyte concentration all increase electrolysis rates.

2009 d) Usually w =e would use an Ag cathode so the Ag+ conc would stay constant in solution. This reaction gives a cell potential of 0V. However, i) if you think about you will see that a spontaneous metal displacement reaction would happen between the Ni and AgNO3. thus we do need to provide a -ve potential to the Ni to prevent it dissolving. ii) A potential of 0V actually means it is in equilibrium, the Ag will ppt and dissolve at both electrodes not plate the Ni. To actually get a silver plate we need to ensure that the reduction (deposition) of Ag only happens at the spoon (cathode) and oxidation (dissolution) of silver only happens at the silver anode - ie a voltage with the -ve terminal at the spoon is needed.

2010 bii) The cathode could be identified by the hydrogen gas or hydroxide ions  BUT HOW could you test for them – ie test with pop test or use a phenolphthalein indicator…

2012 di) Validity means measuring what you intended ie the effect of ONE variable (IV) on the dependent variable. As soon as you change multiple variables you can no longer validly say which changed variable affected the DV. Many people neglected to mention that in a valid test only one variable is changed.

2020 dii) Not the greatest Q for us. All through the Q student were drawing on the reactions at the electrodes until they get to the Q where it specifically states to draw the expected results on your diagrams and everyone stops drawing them on. You should have include 3 diagrams (control and two different variables changed – one in each of the other two pictures). You should have specified the constants and drawn on th results – ie bubbles and Cu deposition showing MORE (or less) depending on what variable you were testing.

Lastly – in their diagram they had a graphite and copper electrode. You should have used the sae chemicals in your example ie the Cu as the cathode th graphite as the anode.

Monday, 2 September 2013

9.4.5 HSC Question Feedback


2001

Q14)
Remember – microscopic membrane filters pores can get clogged – any arrangement that will lead to clogging of the pores is not going to be used.

 

2002

Q26b)

Read the Q! – if it asks you to give answers in mg or mg/L – so you just have to do it! BUT DON’T FORGET SIG FIGS!

Q27)

When  asked to describe the ‘physical and chemical’ processes to treat water – most described all the processes well BUT the fact that the Q said ‘Describe the physical and chemical processes…’ rather than just ‘describe the processes…’ should have been a clue that you needed to identify which were physical and which were chemical. In addition ‘purify’ and ‘sanitise’ were in the Q – this needed o be addressed in general – ie WHY this is needed for drinking water (colour / flavour/ health). Which the definition of these terms is debateable some sources report: purification= removing unwanted particles (eg flocculation, sedimentation, filtering) while sanitation refers to removing pathogens – eg adding chlorine.

 

2003

Q26)  

First you have to link the concept of ‘nutrients’ to nitrate and phosphate (at least N and P) pollution (eg from agriculture or sewage treatment). Then outline the process of eutrophication. When it came to assessing the tests to monitor eutrophication most identified turbidity, BOD, DO and nitrate/phosphate tests as indicators of turbidity and outlined them BUT few assessed them (ie DO, BOD, turbidity indicate if eutrophication IS occurring, while nitrate and phosphate readings indicate whether eutrophication MAY occur) and very few actually said WHAT the readings would be IF there was eutrophication (ie high BOD, turbidity, N and P but low DO). Both the assess and the identification of the typical readings in eutrophication are critical for this sort of question.

REMEMBER  - Always refer to DO as an OXYGEN CONCENTRATION

 

2004

Q21a)

The intro to this question related to ‘water testing’ thus your qualitative and quantitative answer should relate to water testing – ie testing for the ‘presence’ of chemicals vs testing for the actual concentration of chemicals

 

Q21c)

Ba(NO3)2 (aq) (or BaCl2 (aq)) is used to test for phosphate and sulfate (both make a white ppt) BUT you need to specify that the barium phosphate ppt is soluble in acidic conditions but the barium sulfate ppt is not.

& Again – the NH3 we add in the flow charts Is NOT to form a precipitate it is used to neutralise the acid we added inn the previous steps. If phosphate is present it won’t for a precipitate with barium in acidic conditions but will form a precipitate once the acid has been neutralised – hence the addition of the ammonia.

 

2005

Q21b)

AAS is not a CHEMICAL test – take care to read the questions carefully.

Q21c)

We did a whole case study on lead…

A Q for you – which of these two answers - both which take equal time to write would be more likely to score highly?:

1)      Lead ion concentration in water needs to be monitored because it is toxic and if not monitored could cause harm.

2)      Lead ion concentration in water needs to be monitored because it is a neutrotoxin and if not monitored could cause harm.

Q25)

TDS means Total DISSOLVED solids – ie you only want to measure the soluble ions – hence filtering out all the non-soluble solids before evaporating the filtrate to crystallise the dissolved solids. Ie you only use the mass of the solid in the evaporating basin

Q26)

When asked for sources of contamination in a catchment, their effects and treatments:

First - make the features distinct. Don’t talk about all the features, then all their pollutants then all their treatments – this reads like a brain dump and is not clear to the markers that you UNDERSTAND the connections between source-pollutant-treatment. Instead talk about source1- pollutants from that source-treatments for that pollutant. Then talk about source 2 – its pollutants…

Second – an easy strategy is to choose ONE aspect that can cause turbidity (and turbidity is suspended particles NOT ions) eg mining, construction, agricultural soil run off, land clearing/logging = soil erosion, urban areas = excess stormwater run off. And then say how these particles can be removed by coagulation, sedimentation and filtering. THEN choose ONE aspect that can cause bacteria (pathogens) – eg sewage treatment, agriculture (manure, dead animals) and describe how chlorine must be used to treat this.

Finally – don’t jump straight to membrane filters as a ‘one-size-fits-all’ solution to water treatment. It is only used in specialist applications at the moment.

 

2006

Q27c)

 Remember that EDTA reacts with both Mg2+ and Ca2+ (and, as said above, both are assumed to be Ca for hardness analysis) BUT AAS will only test for one metal at a time so the AAS reading for Ca will be less than the EDTA test for Ca

 

2008

Q12)

Remember an estuary has salt water thus TDS will be VERY high. Towns have sewage systems so E coli will be high and DO low

Q17)

This is a question where you have to read and answer VERY carefully. But if you do red it is VERY simple. Identify one feature (eg farmland) link it to one pollutant/problem (soil erosion from cleared land = increased sediment and turbidity in the water) and to a treatment (by flocculating, sedimenting and filtering). Then repeat again for a second feature (eg town, sewage, E.coli, disease, chlorine)

 

2009

Q25a)

Always show data on the graph (draw the lines) –use  ruler and use the scale to determine the EXACT numbers

Q25b)

You must refer to the maximum value – ie each under or over. Then give a reason why one might be well under, one just under and one well-over

Q25)

No matter how good your answer is – if you don’t use the proper chemistry terminology – ie you don’t say ‘eutrophication’ – you wont get full marks. Also – re a ‘water quality issue’ NB that eutrophication and algae affect the taste, odur and can cause disease.

 

2010

Q10)

You need to know your ion testing. Ba’s flame colour is APPLE GREEN and it forms insoluble Ba-sulfate. Cu’s flame colour is EMERALD GREEN and copper sulfate is SOLUBLE!.

Q25)

Make sure you define both correctly (DO is a concentration of dissolved oxygen) BOD is the amount of oxygen used by microorganisms to decompose the organic matter in water over a 5 day period. Make sure you say why BOTH need to be monitored – DO needed for life (DO needed to measure BOD), BOD sign of organic pollutants/eutrophication…

Q31ai)

See 2005 Q25

Q31aii) Silver chloride is a WHITE ppt that darkens in sunlight (ie our ‘photography’ experiment from last year

Q31b)

Hardness- ie Ca2+ ins often occurs in bore water or water from a limestone aquifer or waterway. Limestone is CaCO3 so = lots of Ca in the water

 

2011

Q28)

For your two tests you need to

·        Outline them

·        ID if physical or chemical

·        ID the principle. Here are some easy ones suspended solids scatter light (turbidity test – physical) dissolved solids conduct electricity (TDS probe – physical), dissolved solids crystallise when the solution is evaporated (TDs – physical), Ca and Mg react with EDTA in a 1:1 ratio (Hardness – chemical)

Q31)

Impressed with the fact that mot used data from the table and made plausible reasons WHY the TDS etc increased on Tue and bacteria on Thu (one possibility is high rainfall = erosion on Tue and an consequent sewage overflow on Thu).

Thursday, 25 July 2013

Trial (& HSC) Study Tips


STRATEGY #1

Throughout the year you have been doing a huge amount of work on the HSC booklets.

I tried to do my part by writing comments to highlight any questions that contained tricks, needed a specific approach/strategy or were challenging for the class as a whole.

Now it is time to make those booklets, those comments and all that hard work to pay dividends.

This works for Pre-Trial and Pre-HSC.

It is a tried-and-tested Dr Burg approved method of study.
 
1) Get out all the HSC booklets from the year (even if you haven't done them, this is still a valuable exercise).

2) Get some paper (draw up 2 columns), a pen and 2 highlighters of different colour.

3)Start with one Focus-Area booklet (I'd start with 9.6.7 and work backwards to 9.2.1).

4) Click on the link to the comments - the links are at the bottom of this post below strategy 4.

5) Go through the HSC booklet and look at all the questions that I specifically made a comment on.

6) Read the question. See if you can remember the trick, the strategy, the problem or just the key things to say for this question. Check my comment - see if you have an "ahhh, that's right" moment.

7) If you remembered all the tricks, strategies, and are happy with that Q - move on.

8) If you thought to yourself "I know that topic pretty well, but I'd better check this again to remind myself those tricks" then highlight that question one colour. Also make a note of the Focus area, year and Q # in one column of your paper (“revise”).

9) If you thought to yourself "I really need to do this again" highlight this in the other colour and make a note (Focus area, year, Q#) in the second column (“redo”) on your paper. You can also do this for questions you got no/v.low marks for first-time around  if you wish.

10) Don't revise or redo the questions now, just keep working through the focus areas as above.

11) Once you have reached the end you will have a list of questions to revise and a list to redo.

12) In your Chemistry study time redo the "redo" questions – using whatever resources you need until you understand the concept/question. Then it can be shifted into the revise column.

13) At the end of study sessions (or for a pre-bedtime-routine) read over the "revise" questions.

14) Why this strategy can work:

a) It is thorough. All the important concepts have been covered in HSC questions so you are covering the course by looking at the questions.

b) It is study. By revising the questions and comments you are bringing all the strategies, concepts, tricks back into your short/medium term memory and strengthening their place in your long-term memory.

c) It is high-gain. By redoing the questions that trouble you, you are focussing the bulk of your time into the areas where you can make the biggest improvements.

 
STRATEGY #2

1) Focus-area by focus-area make a list of the things &/or questions that you DO NOT want to see in the Trial/HSC. I.e. you are making your own personal “HSC-paper-from-hell”.

2) Study those topics as though you *knew* that the list was the exact paper you were going to have to sit.

3) You have just negated your “HSC-paper-from-hell” and have turned your weaknesses into strengths.

 
STRATEGY/TIP #3

At the end of the Literacy/Numeracy assessment I noted to you all that there were a few questions that very few students submitted (Q4, Q7, Q9, Q11, Q14, Q17, Q19, Q21, Q23, Q24, Q26, Q27, Q37, Q38) At the time I remarked how I really need some extra assessment information on those topics and that it was lucky that there was an assessment exam coming up.
I found it interesting that when I marked the 9.4.2 and 9.4.3 HSC booklets that the students who had done the essays on the Haber process, impacts of the Haber process, AAS techniques, AAS trace elements and pollution wrote very good extended response answers on those topics. Make of this what you will, but I am still happy to check, correct and provide feedback on ½ page essays…


 
STRATEGY #4
This is really an ‘exam-room’ tip that I thought of when writing the 9.3.4 Feedback.

You need to get in the mindset (to be hyper-aware) that that you need to distinguish yourself. The only way to distinguish yourself is through what you write. No matter how much you know - if you don’t include detail, address the verb, define terms etc, there is no way of distinguishing you from someone who knows nothing. Ask yourself :

  • Could someone who was trying to ‘wing it’ write my answer?

  • What have I added that cannot be ‘winged’ that makes me stand out?


HSC FEEDBACK LINKS















9.4.5 – Water Analysis & Treatment



9.6.3 – Electrolysis



9.6.7 – Conservation & Restoration
 
Remember this - All it takes is "Just Work"!
 
 
 
And watch this before your study/exams etc - How could you not want to do well and dominate the state after watching this ?

 
 
 

Monday, 22 July 2013

9.3.4 HSC Q Feedback


2001

Q21) Key idea – IONS in solution allow charge flow (conductivity) – at start barium and hydroxide ions carry current, but their concentration and thus conductivity decrease as acid is added.. At equivalence point = no free ions = no conductivity. After equivalence point increasing acid concentration increases sulphate and hydrogen ions = increasing conductivity.

2003

Q23a) You would think that I had never tried to trick you by giving you volumes in mL rather than litres. CONCENTRATION CALCULATIONS ARE IN LITRES!

Q24) Always define the key Chemistry term – ie neutralisation. Also give an example chemical and you could possibly also talk about skin spills.

2004

Q22b) As inconvenient as it sometimes is, you have to answer the question asked. If they ask for equations to show why dihydrogen phosphate is amphiprotic you have to do it. You can’t just substitute other chemicals!

2005

Q9) Buffers are a mixture of a weak acid and its conjugate base. Conjugate bases have ONE less proton than the acid (not two, hence dihydrogen phosphate and hydrogen phosphate are buffers but dihydrogen phosphate an phosphate are not).

Q21) Try and link the scientists together specifically noting what the previous model couldn't explain (ie in the scientific method new theories are proposed when old theories can't explain all observations), eg Lavoisier said they contained oxygen based on his experiments but Davy disproved this when.... Arrhenius developed Davy’s theory by noting that acids ionise to produce H+ in aqueous solutions.... But could not explain amphiprotic substances, acidic salts or acids in non-aqueous solutions. BL theory explained acids in all solvents by noting that they were proton donors. It is critical that you note that BL realised the importance of the solvent. Ie a substance would be an acid in a solvent IF it could donate a proton to that solvent. It is vital that you use chemical equations. Eg show how Arrhenius explained the acidity of HCl (by producing hydrogen ions) compared to BL (producing hydronium ions). And this means you have to be careful, Arrhenius said acids ionise to produce hydrogen ions NOT hydronium ions (that is  BL concept).

2006

Q9) Equivalence I when equal # of hydroxide and hydrogen ions have been added. Many strong acid/base neutralisation reactions are not 1:1 in terms of acid to base molecules (eg H2SO4:NaOH = 1:2) but are always 1:1 H+ to OH-.

Q11) Arrhenius modelled acids as chemicals that ionised to produce hydrogen ions. The higher the % ionisation the stronger they were. pH was a concept that was developed from his model but was not part of is model.

Q21b) To show a given salt is acidic (or basic) you have to show one of its ions reacting with water to donate (or accept) a proton to produce hydronium (or hydroxide). The parent acid/base argument is useful for titration questions only. BUT NB these salts are weak acids and bases – the equations MUST have an equilibrium sign.

2007

Q25) Show two equations to show it is amphiprotic(ie reacting with OH- and H3O+) and could also that it is cheap (not absolutely critical but most people overlooked it).

2008

Q8) Arrhenius said that acids ionise to produce hydrogen ions, BL said they were proton donors

Q26) Define key terms ie define buffer

Q27b) See 2006 Q21b above

Q28c) NEVER, NEVER, NEVER use c1v1=c2v2 unless it is a dilution.

*Find the moles of one species

*Find the moles of the other via a mole ratio

*Do the calculation to find what it is you are asked to find.

2009

Q14) Excellent Q to do – make sure you can do this Q. I have a feeling a similar one is coming in this year’s HSC

Q21) – an excellent Q to do again for revision

a) The more base that has to be added to neutralise the more moles of acid there are. Because they are both in equal volumes you can determine their relative concentrations. The weaker acid will have an equivalence point at higher pH.

d) Answer the Q. The end point ideally happens at the exact equivalence point but as long as the colour change occurs within the ‘steep’ part of the curve, the endpoint (ie amount of base added hen the titration stops) will match the equivalence point.

2010

Q8) Davy said that acids contained replaceable hydrogen. Arrhenius said they IONISED in water to produce hydrogen ions.

Q28) You should show your calculation for the mass of standard. You must say how the conical flask, pipette and burette are cleaned. You have to say which indicator is used and should explain why. Don’t forget that titrations are repeated until 3values within 0.1ml and averaged.

2011

Q15) At equivalence point the moles of H+ = moles of OH-. The number of moles of acid base needed only depends on the mole ratio, not on strength.

Q18) – this is very similar to 2001 Q23

Q26a) You actually need to calculate both concentrations (from solid and from titration) to show how the values are different, not just say that NaOH absorb water and CO2 from the air.

Q29) If asked a Q about a scientist’s acid theory, you must outline the theory. Ie what ar the basics of BL and Arrhenius theory. In this case re why we still use Arrhenius NB that most everyday acid are aqueous and the Arrhenius model is simple and convenient to use (eg calculating pH, comparing strength etc).

Monday, 25 March 2013

Experiment #13

'Results' shown here in glorious colour.

Sulfuric Acid


Hydrochloric Acid


Acetic Acid
(systematically known as Ethanoic acid))


Citric acid
(systematically known as 2-hydroxypropane-1,2,3-tricarboxylic acid)

Worksheet

Q2) & Q3)
Unless the acid/base is strong (ie NaOH, KOH, HCl, HNO3, H2SO4) you MUST use the equilibrium arrow. AND you must include states!

Q2) & Q3) & Q4) & Q5)
  • When an acid donates a proton it is losing one unit of positive charge. Thus the conjugate base must have one less positive charge. Eg H2SO4 (aq) + H2O(l) => HSO4-(aq) + H3O+(aq) The conjugate base (HSO4-) has one less H and one less positive charge than the parent acid (H2SO4)
  • When a base accepts a proton it is gaining one unit of positive charge. Thus the conjugate acid must have one more positive charge. Eg NH3(aq) + H2O(l) => NH4+(aq) + OH-(aq) The conjugate acid (NH4+) has more H and one more positive charge than the parent base (NH3)
  • Simply put - when writing chemical reactions the atoms AND charge must balance.
  • Always show states

  • Q6 & Q7)
    It is good practise to show the H+ ion transfer in acid/base reactions - this is especially tru if you are having trouble identifying the conjugate pairs. The acid is what has donated the proton. The conjugate base is the resulting species that has one less H+. Similarly the base is the substance that accepts the proton. The conjugate acis is that new species with one extra H+.

    Q8)
    For stepwise dissociation, there can only be as many ionisations as there are 'donatable' protons. Citric acid is triprotic thus there will be three ionisations. Don't forget that the conjugate bases produced by these ionisations will have one less H  and one less + charge each time. Finally - the questions specified that these were all weak acids so use the appropriate arrows.

    Q9)
    NEVER show an amphiprotic substance donating AND accepting protons to water. Water is either more acidic or more basic than the amphiprotic substance not both. Eg bicarbonate ions will always accept protons from water (making the solution slightly basic), but will not donate them to water.  SO when showing how a species is amphiprotic write one reaction where it is accepting protons from H3O+ (strong acid) and one where it is donating protons to OH- (strong base).

    Summary

    The expression/language/communication in these summaries was generally very poor and many did not answer the questions that were asked. I can't stress enough how important it is to express yourself clearly in Chemistry. You need to know your definitions and terms thoroughly and  need to use correct definitions and explanations. You notes are full of examples of explanations and definitions designed specifically for the HSC course. Please use them. But, as disappointed as I am, I now have an excuse to post my new Chemistry pic!

    (A) You MUST know where the double bonds are in citric acid and you must know which H is removed from acetic and which H's from citric acid. You must remember to i) include and ii) draw correctly the hydroxyl group in citric acid. You were asked to draw the acetic acid and its conjugate so you need to do this and label them as such. In addition, the conjugate base should have a – sign next to where the H was removed. Finally - you needed to draw 'ball-and-stick' models, structural diagram are not sufficient (and it using coloured circles you need to include a key).

    (B) Don’t even think about copying and pasting anything into a experiment summary ever again.

    (C) This is the most important concept. It is vital you use the correct wording. Poor selection of words conveys that you don’t understand the difference between strong and weak, because IF you completely understood the difference THEN you would not use poor wording. Strong means that EACH acid molecule is ionized. It does NOT mean that ‘every hydrogen is removed’, or ‘all hydrogen’s ionized’. It is important that you understand this distinction. Weak acids have only SOME of their molecules ionized (or some of their molecules donate a proton). This is very different to the incorrect ‘ only some of their hydrogen’s are ionised’, or 'only some of the hydrogens came off the molecule; or ‘some of their hydrogen’s are removed’.

    (D) Give the % ionisation equation! and make sure you define it correctly (see above). Also you need to give examples - ie you should specify the exact % ionisation for hydrochloric, acetic and citric acids.

    (E) You need to say WHY a BASE is formed when an acid donates a proton (and vice versa) and you must define what a CONJUGATE PAIR is – i.e. answer the question

    (F) You must explain WHY strong acids/bases produce very weak conjugates and why weak acids/bases produce weak conjugates – not just state that they do – ie again, answer the question

    (G) The conclusion must answer the aim. SO -1) What did you use to model acids?, 2) How did you use those models to model strong and weak?

    (H) Don't forget that you have to explain why structural formulae (diagrams) are more useful than molecular formulae for organic compounds. i) It allows you to see what the functional group is and where its is ii) it helps you to predict the properties of the compound. iii) there are many isomers of organic compounds and the structural diagram allows you to clearly determine the isomer. Eg see here for all the isomers of this simple molecular formula C4H8O2




    Sunday, 17 March 2013

    Experiment #12

    Results Table

    Errors in pH measurement lead to big errors when calculating % ionisation. That is because the formula
    [H+] = 10-pH  being an exponential gives big differences in [H+] calculations for small differences in pH
    In addition because the pH probes accuracy is +/- 0.05 pH units that alone can lead to large errors in %ionisation calculations. I have calculated the range of % ionisation values for each reading so you can see how a big a difference +/- 0.05 pH error can make. In your summary you need to calculate the [H+] and % ionisation using the pH reading given in the table (but you may wish to note the range).
    NB - I went back nd remeasured some of the values after I did my calculations as some were very different - one of the probes was not calibrated correctly and I think that the times that students tested the solutions with the probe not fully submerged made a difference too.
    CHEM
    CONC (mol/L)
    pH (+/- 0.05)
    HIGH (%I)
    LOW (%I)
    NH3
    0.1
    11.6
    3.5
    4.5
    NaOH
    0.1
    12.9
    70.8
    89.1
    -
    -
    -
    -
    -
    H2SO4
    0.001
    2.8
    141.3
    177.8
    HCl
    0.001
    3
    89.1
    112.2
    H2SO4
    0.01
    1.9
    112.2
    141.3
    HCl
    0.01
    2
    89.1
    112.2
    C6H8O7
    0.1
    2.1
    7.1
    8.9
    CH3COOH
    0.1
    2.7
    1.8
    2.2
    H2SO4
    0.1
    0.9
    112.2
    141.3
    HCl
    0.1
    1.1
    70.8
    89.1
    HNO3
    0.1
    1
    89.1
    112.2
    HCl
    1
    0.1
    70.8
    89.1
    
    Summary
    A)     Look at your Focus 3 booklet. Identify that pH is a function of [H+]. Identify ALL the factors that can affect pH. Identify specifically how they affect [H+] and thus pH (eg increasing concentration increases [H+] and thus decreases pH). Make sure you don’t make the mistake of saying that increasing the acidity increases the pH. More acidic means a LOWER pH.

    B)      You need to identify the natural source AND a practical application of each acid and base. Eg CaCO3 being found in limestone is not a ‘use’ of CaCO3

    C)      You need to explain why all factors that can effect pH must be kept constant if using pH to compare acid strength. This comes straight from our notes.

    D)     Conclusions are not personal. Conclusions should state the findings – ie what was the order of strength of the four acids?

    E)      The diagram must have equal numbers of anions and cations. It must have a key and the cations MUST be H+

    F)      Your table needed to include [H+] with units (which you need to calculate from pH) and the degree of ionisation of each acid (which you also need to calculate).

    G)     You need to show all equations used for relating [H+] and [OH-] to pH (4 minimum).

    H)     For the USES of acids in food: identify the acid and what it is used for. Saying acetic acid is in vinegar is not a use – instead you need to say the acetic acid in vinegar is used for…