Showing posts with label acid-base titration. Show all posts
Showing posts with label acid-base titration. Show all posts

Friday, March 25, 2022

Chinese Milk Scandal

 When we buy food from a shop, we assume that food is safe to eat, but sometimes it isn't!

In 2008 six babies died from kidney stones and an estimated 54,000 babies were hospitalized in China after being fed "Infant Formula" (baby milk) adulterated with melamine, an industrial chemical. It is thought that about 300,000 babies in total were affected by what came to be known as the "Chinese Milk Scandal".

Why was melamine added to Infant Formula? And why did it take so long to discover its addition?

Read more in this edition of AUS-e-NEWS:

Subscribe to AUS-e-NEWS at https://www.ausetute.com.au/ausenews.html

 

Tuesday, December 22, 2020

What is an indicator?

What is an acid-base indicator?

What does it do?

Where do we use acid-base indicators?

These and other questions about acid-base indicators can be answered at 

https://www.ausetute.com.au/indicators.html

AUS-e-TUTE Members also have access to the game, test and exam with worked solutions on this topic.

Join AUS-e-TUTE Today!

Sunday, August 2, 2020

Weak Acid - Strong Base Titration Curves

A titration of a weak acid with a strong base results in a titration curve with some notable features, including:
  • buffer zone (weak acid in equilibrium with its conjugate base)
  • point where pH = PKa which can be used to determine pKa, and hence Ka, for the weak acid
  • equivalence point where pH > 7 due to the hydrolysis of the anion

Find out more at https://www.ausetute.com.au/titrcurvwasb.html

AUS-e-TUTE Members should log-in to use the new tutorial, game and test.

Thursday, June 4, 2020

Question Impossible?


See if you can answer it ...

Boric acid, which is a weak acid, was titrated with standardised sodium hydroxide
solution.
Which one of the indicators listed below would be the most suitable to use in this
titration?


  Indicator Range of colour change
 (pH)
 (a) thymol blue 1 – 3
 (b) bromocresol green 3.8 – 5.4
 (c) cresolphthalein 8 – 10
 (d) alizarin yellow 10 – 12

(Note: no further information was given in the question nor in the accompanying Data Book).

You've probably narrowed the answer to either (c) or (d) using a couple of common assumptions:
  • these are aqueous solutions of acid and base
  • the temperature of the solutions is 25C
The salt of a weak acid and a strong base in aqueous solution at 25C will have a pH greater than 7.
So, what now? We need more information, like the value of the acid dissociation constant for boric acid and some information about concentrations and volumes.
Boric acid is a weak acid, Ka = 5.8exp-10 (this information was not provided!)
Because Ka is so low, boric acid is essentially a monoprotic acid, so the salt produced is essentially NaH2BO3
Sodium ions will not hydrolyse but H2BO3- will hydrolyse.

H2BO3- + H2O --> H3BO3 + OH-

Kb for the hydrolysis of
H2BO3-:
Kb = Kw/Ka
= 1exp-14/5.8exp-10
= 1.7exp-5
We need to know the concentration of the salt,
 this wasn't given in the question,
 so we are going to assume a 1.0 mol/L solution
(because the numbers are nice)
[
H3BO3] = x
[OH-] = x
[H2BO3-] = 1.0 - x
and assume x is negligible compared to 1.0
 therefore
[H2BO3-] ~ 1.0

Kb =
[H3BO3][OH-]/[H2BO3-]

1.7exp-5 = x2/[1.0]
take the square root of both sides:
x = 4.1exp-3 = [OH-]
pOH = -log10
[OH-]
= -log[4.1exp-3]
= 2.4

For aqueous solutions at 25C:
pH = 14 - pOH
= 14 - 2.4
= 11.6

So..... drum roll please .... the answer is (d)


Ofcourse, if the concentration of salt was 1exp-5 mol/L,
the pH of the solution would be 9.1 ....
and then the answer would be (c)

If you were unfortunate enough to sit this exam...
 then the answer according to the examiners report was (c) ...
but no details of how they arrived at this answer are provided.

Saturday, March 7, 2020

Indicators for Strong Acid - Strong Base Titrations

When a strong acid is added to a strong base the products are water and a salt.
Water is neutral, that is [H+(aq)] = [OH-(aq)]
 (or [H3O+(aq)] = [OH-(aq)] if you prefer)

The salt of a strong acid and base is made up of a cation that will not react with water to any appreciable extent, and an anion that will not react with water to any appreciable extent, so this salt does not affect the  [H+(aq)] and [OH-(aq)] in the water, that is, the aqueous solution remains neutral.
At 25°C, Kw = [H+(aq)] × [OH-(aq)] = 10-14
Since [H+(aq)] = [OH-(aq)]
Kw = [H+(aq)]2 = 10-14
√[H+(aq)]2 = √10-14
[H+(aq)] = 10-7 mol L-1
 So, at 25°C the pH of this salt solution will be pH = -log10[H+(aq)] = -log10[10-7 ] = 7.0
A suitable indicator is one that changes colour at around pH = 7.00
Suitable indicators, for example, are bromothymol blue (colour change between 6.7 and 7.6) or phenol red (colour change between 6.8 and 8.4)

Phenolphthalein changes colour between pH 8.3 and 10. Phenolphthalein is NOT an appropriate indicator for a strong acid - strong base titration.

If we add a drop of phenolphthalein indicator to an aqueous solution of strong acid, the pH will be less than 7 and the solution will remain colourless. As we add strong base, hydrogen ions react with excess hydroxide ions to produce salt and water, so the pH increases. At pH = 7.0 all the strong acid will have been neutralised by the addition of strong base, BUT the phenolphthalein indicator will not have changed colour!
Phenolphthalein will not change colour until an excess of strong base (hydroxide ions) has been added and we have overshot the equivalence point for the reaction. The volume of strong base we record in this experiment will be too large!.

In strong base such as an aqueous solution of sodium hydroxide, the pH will be high and a drop of phenolphthalein indicator will turn the solution pink.
As we add a strong acid such hydrochloric acid, we will be consuming some of the hydroxide ions, and decreasing the pH. Somewhere between pH 8.3 and 10 we will decide that all our base has been neutralised by the acid because the indicator is now colourless instead of pink. But the reality will be that there is still excess hydroxide ions in solution waiting to be neutralised by the addition of more acid, so the volume of acid we have added, as indicated by the colour change of the indicator will be too low!

Learn all about how to choose an appropriate indicator for different types of acid-base titrations ar
https://www.ausetute.com.au/indicata.html

Sunday, June 9, 2019

Conductometric Titrations

Trying to titrate a weak acid with a weak base using an acid-base indicator is .... annoying!
The end point of the titration is extremely difficult to guage.
If only there was a better way ....
There is!
Let us introduce you to acid-base conductometric titrations in AUS-e-TUTE's new tutorial, game, test and exam resources. AUS-e-TUTE Members should log-in to use these new resources.
Non-members can currently access the "free-to-view" tutorial at https://www.ausetute.com.au/conductab.html

Friday, March 25, 2016

Acid-Base Equilibria and Beginner Teachers

Cathy is a Year 12 student in a Brisbane school (capital city of Queensland, Australia). Last week she had a chemistry exam, the topic was equilibrium which included acids, bases and acid-base titrations. I met her on her way to school on the morning of this exam. When I asked her if she felt confident about her exam, I was horrified by her response,
"Sort of. I've got a new teacher this year and she's not any better than the one I had last year. We did an experiment, she said it took too long so we didn't do any more."
Seasoned teachers are used to:

  • student claims that their teacher is "no good" (especially if the student is performing poorly)
  • student exaggeration (only 1 experiment in a whole term of equilibrium, surely not!)
"Oh come on", I said in my best 'you're kidding me' voice, "you studied equilibrium for a whole term and only did one experiment?"
"Yeah", she confirmed, "we watched a video on titration though".
"Didn't you do a titration experiment?"
"Nah. She said we didn't have time."

Even allowing for the possibility of student exaggeration, the thought that you would play a video showing someone else performing a titration rather than giving your own students the opportunity to carry out even a simple titration, is, quite frankly, appalling. 

From Cathy's description of the teacher I assume this is the teacher's first year out teaching (beginner teacher). Reflecting on my own first year of teaching (a long, long time ago), I remember struggling to meet the requirements of the chemistry syllabus in the time-frame allowed, and, I also remember that while teaching the techniques of titration was time consuming, the students learned more in a few practical sessions than they learned during the whole of the preceding theoretical lessons, and once they have mastered the techniques they can be put to use in real-world problems.

A typical sequence that is often taught for (monoprotic) acid-base equilibria assumes prior knowledge of solutions, concentration (molarity) and equilibrium concepts and calculations (including self-dissociation of water, Kw ):
  1. What are the properties of acids and bases?
  2. How do we define an acid and a base?
  3. What is meant by the terms "strong acid"  and "strong base"?
  4. How do we measure the strength of an acid or a base (pH scale)?
  5. What happens when you add an (Arrhenius) acid to a (Arrhenius) base (neutralisation)?
  6. How much (Arrhenius) acid do we need to add to a known amount of (Arrhenius) base in order to neutralise it (acidic, basic, neutral solutions)?
  7. Discussion of titration techniques, including preparation of a standard solution.
  8. Performing a strong acid - strong base titration.
  9. Using the results of the experiment to calculate the concentration of the unknown acid or base.
  10. Perform calculations for each 1 mL addition of strong acid to strong base in the titration experiment and graph the results (strong acid - strong base titration curve)
  11. Discussion of weak acids (Ka).
  12. Discussion of other acid-base reactions (proton transfer reactions) and other titration curves
  13. What indicator should you use for a particular acid-base reaction? (optional, how does an indicator work)
  14. Titration of weak acid - strong base (such as determination of acetic acid in vinegar)
If you see your students 4 or 5 times a week, this teaching program for acid-base equilibria will take about 4 weeks using a traditional, structured approach. If you have the luxury of being able to time your practical work so that it occurs in the correct sequence, and take time to link the practical work to the theoretical concepts, your students have a good chance of understanding and being able apply the concepts to unfamiliar problems.
If you don't do any experimental work, you could probably bowl it over in 2 to 3 of weeks, and be faced with a lot of bored students wondering why they ever took a course in chemistry.
If you take a student-centered constructivist approach (for example, start with the questions  like "what gives vinegar its tangy taste?",  "if acids are corrosive and burn skin, how come you can drink vinegar?",  "how can you measure the strength of an acid?", "how can we determine which brand of vinegar has the greatest concentration of acetic acid?"), be prepared to add another week (unless you give the students a lot of reading/research for homework). The benefits, however, are enormous. Your students are more likely to be engaged with the content and "on task", they will have to be able to justify decisions they make in order to design and perform experiments thereby linking concepts and practical work, and because they "invest" in the whole learning process they are more likely to be apply the understanding and knowledge gained to other problems.

So, if you are new to teaching acid-base equilibria, here a few suggestions:
  1. Even if you firmly believe that constuctivist approaches to teaching are the most effective way to teach chemistry, be prepared to spend your first year of teaching chemistry taking a more traditional approach, using guided questioning to lead students towards the experiment(s) you need them to do (syllabus requirements) while still giving them "ownership" of the experiment and its results. Keep a list of the misconceptions you come across when you teach, this will help you be better prepared for next year. As you feel more confident in your ability to meet the syllabus requirements within the time you have, and you have a better feel for the misconceptions you will meet, you can start "loosening your hold" and give more time to truly constructivist approaches.
  2. Let the students do as much practical work as possible (students not only need to be exposed the practical techniques of chemistry, they need to do the experiments in order to fully appreciate the significance of what you are trying to teach them). You also need to devote time to discussing the results of their experiments with them, and reinforcing the concepts, calculations, techniques etc involved. 
  3. Spend time discussing the self-dissociation of water (that is, it is a lesson in its own right, not just a passing reference before you discuss acid-dissociation). Students will have been exposed to an "acids and bases" topic sometime between Years 7 and 10, but even so, many of them may still think that an acid has a pH less than 7, a base has a pH greater than 7, and that a neutral substance has a pH of 7. Believe me, it can be an uphill struggle to separate the two concepts of "acid, base, neutral" from the concept of "pH" in a student's mind (and if you don't believe me, think about the number of times you have seen/heard advertisements for products which talk about the "neutral pH" of skin/hair etc). If the students do not have a good grasp of the self-dissociation of water then they will not understand the pH of  aqueous solutions. (And a word of caution, just because a student can calculate the pH of an aqueous solution of base at 25oC, it doesn't mean they understand the relevance of pH + pOH = 14, or [H+][OH-] = 10-14, and if you want to test this statement, ask you students to calculate the pH of 0.001 M NaOH(aq) at 50oC, or ask them to find the pH of 0.01 moles of HCl(g) dissolved in 1 L of ethanol and see what happens, because the chances are they will simply do a pH + pOH = 14 calculation without even thinking about it!)
  4. Spend time making the distinction between "strong acids", "weak acids", "dilute aqueous solutions of acids" and "concentrated aqueous solutions of acids" (similarly for bases) because once again, you are likely to have an uphill struggle to separate the two concepts "strength of an acid/base" and "concentration of an acid/base". Remember, they have already been exposed to statements such as, "I need a cup of strong coffee", or, "this cordial is a bit strong" which, in chemical terms should be "I need a cup of concentrated aqueous solution of coffee (or cordial as the case may be)". On the other hand, they have also been exposed to ads which say things like "concentrated laundry detergent" which is a slightly more appropriate use of the technical term "concentrated" (although I do remember one example that used "concentrated laundry liquid" which introduces the other problem of the loose usage of the word "liquid" instead of "solution"). One way to do this is to give each pair of students a bottle of acetic acid labelled with its concentration, and have them measure its pH with a pH meter. Also provide them with volumetric flask of HCl(aq) of known concentration (say 0.1 M) and have them measure its pH, then have them perform sequential 1:10 dilutions and measure the pH at each stage say they can see that pH is dependent on the concentration of the strong acid and that you can reach a point at which the pH, and therefore the concentration, of a strong acid is the same, and even greater than, the concentration of an aqueous solution of weak acid. When you tabulate the class results and ask them for an explanation be prepared for many of them to believe you somehow "tricked them", it can take time for them to break the strength/concentration misconception and replace it with a more appropriate separation of the two concepts. If the students do this activity themselves, it will easily take a lesson, if you do it as a demonstration it will take about 10 minutes, BUT, it is better for the students to do it themselves partly because it reduces the instances of "there must be a trick in this" thinking, but mostly because they can see the pH change with the concentration and they are going to have to justify that all the way to the point at which the pH of the strong acid is  greater than the pH of a weak acid.
  5. Related to point 2 is the common misconception students may have that when you add an acid to a base you end up with a neutral solution that has a pH of 7. Personally, I think the best way to deal with this is to let the students work it out for themselves before you attempt to explain it to them. For example. give each pair of students a bottle of methyl orange indicator (you will need a fair degree of tolerance in establishing the end-point so don't use a pH meter) and a conical flask and have them add a 10.00 mL aliquot of standardised 0.1 M NaOH to the flask and record what happens to the indicator colour. Have them calculate the moles of hydroxide ions in the flask, as well as calculate the pH of the solution (so they are convinced the indicator is giving a true reading). Then give each pair a 100 mL volumetric flask containing 0.1 M monoprotic acid (some will get a strong acid such as HCl(aq), some will get a weak acid such as acetic acid). . Have them calculate the volume of acid they will need to add to the NaOH(aq) to neutralise it. Have them add this volume (straight from the pipette to the flask), give it a swirl, and record the colour of the indicator. Tabulate the results on the board (yellow vs red). Ask them why some changed colour and some didn't (be prepared to let the students with weak acids try adding more acid, many will believe they made a mistake in the calculations or in adding the solutions), if the students do not come to the realisation that only students with strong acids got a colour change at neutralisation, you can use questions to help guide them. I have found this is a far more effective method than just "telling them" and it need only take 15 minutes if all the solutions and equipment are prepared before hand AND you don't expect them to write it up as a prac (a demonstration takes even less time, but may not be quite as effective, that is, some students will believe you have somehow "tricked" them).
  6. Have the students perform the calculations that will enable them to draw a strong monoprotic acid - strong base titration curve. If you have a class of 20 students, they only need to do one of the calculations each, you can tabulate the results and then they can graph the class results. There are a number of reasons for this, it reinforces the nature of the neutralisation reaction, stoichiometry, and of "limiting reagents" and "reactants in excess". It is also enables them to come to a greater understanding of the shape of the curve than if you just present it to them and discuss key points. Finally, if the students do not have a good grasp of why titration curves are the shapes they are, they will have a much harder time coming to terms with the nature of different indicators and why some indicators are more appropriate than others for particular titrations.
  7. Do use "real-world" examples. The acetic acid concentration of brands of vinegar is not hard to do, and empowers them (if you have mothers whinging that their daughter will now only let them buy brand X because its better value because it has a higher concentration of acetic acid than other brands, then pat yourself on the back for a job well done!) If you are in a position to be able to safely determine the concentration of sulfuric acid in a lead-acid battery, then this is also not hard to do (but check whether it can be done at your school). Similarly, you will find concentrated HCl(aq) available at you local hardware store (for cleaning bricks) or pool suppliers (for addition to pools) and, if your safety guidelines allow, you can determine the concentrations of these.If you are prepared to take your students through back titrations (indirect titrations) then a wealth of new "real-world" opportunities is open to you.
  8. Finally, do not deceive yourself. It is NEVER about what you "teach", it is ALWAYS about what the students "learn". YOU can make up time by giving the students notes you have prepared for them, making them read stuff for homework, making them watch a 30 minute video instead of doing a 2 or 3 day prac, then you can happily tick this off on your list of things to teach, BUT, you must also find out what the students have learned, because you may very well find out that you have been a bit hasty in ticking something off your list! 

Friday, July 17, 2015

HCl as a Primary Standard?

Question: Why is HCl not suitable as a primary standard?
Answer:  There are three main reasons why HCl is not suitable as a primary standard:
  • HCl is not a solid at room temperature and pressure. 
  • HCl cannot be obtained at a very high purity.
  • HCl does not have a high molecular mass.
You can find out more about what makes, and does not make, a primary standard at:
http://www.ausetute.com.au/titrstand.html

Tuesday, June 23, 2015

Which of the following is an acid-base indicator?

Question: Which of the following is an acid-base indicator?
  1. hydrochloric acid 
  2. sodium hydroxide 
  3. water 
  4. phenolphthalein
Answer: Phenolphthalein is an acid-base indicator
  1. Hydrochloric acid is an acid
  2. Sodium Hydroxide is a base
  3. Water is neutral

Sunday, June 21, 2015

What is the best indicator for titration?

Question: What is the best indicator for titration?
Answer: That all depends on what you are titrating!

If you doing an acid-base titration, then you will need to know the relative strengths of the acid and base you going to be using.
Once you have determined an approximate pH for the equivalence point of the neutralisation reaction, you use this as the pH of the endpoint of the titration in order to determine the best acid-base indicator to use.

Wednesday, January 7, 2015

Concentration of Acetic Acid in Vinegar

Here's a strange thing. Most adults wouldn't dream of drinking wine that has been oxidized and "gone bad", just the smell is likely to put most people off! The same people, however, probably have no objection to consuming wine that has been deliberately oxidized, bottled, and marketed as vinegar.

Ofcourse, the chemistry of the oxidation of a mixture like wine is quite complex, but the most important constituent of the mixture is acetic acid (also known as ethanoic acid).

Determining the acidity of your vinegar, or how much acetic acid (ethanoic acid) is present in your vinegar, is quite easy. It's just a simple acid-base titration, and AUS-e-TUTE has just added new resources to help you understand how you can use acid-base titrations to find the concentration of acetic acid in vinegar.

AUS-e-TUTE Members have access to the new tutorial, games, test and exam.

If you are not an AUS-e-TUTE, you can take a sneak peek at the tutorial here