In this lesson, I learned about some basic properties of acids and alkalis, as stated in the title. I learned that universal indicators and natural indicators change colour based on the pH of the solution they are in. I also learned about the effect of acids and alkalis on Methyl Orange and Phenolphthalein. I read that such indicators have a sharp change in their colours and are used in a kind of volumetric analysis known as titration. Universal indicator is not good for titration because its change in colour at the end point of titration is not sharp. One of the 16 Habits of Mind states the need for accuracy and precision. If the change in colour is not sharp, we cannot get an accurate end point. I read that the error for titration is only 0.1ml thus a sharp change is needed.
Lesson 2: Strength of Acids and Alkalis
In this
lesson, I learned about how the strength of acids and alkalis affect its
electrical conductivity. Strong acids and alkalis disassociate and ionize
completely in water. For example, the gas hydrogen chloride ionizes completely
in the presence of water:
HCl (aq) à H+ (aq) + Cl-
(aq)
Weak acids
and alkalis disassociate and ionize partially in water. Such acids and alkalis
prefer remain as molecules rather than ions. Organic acids in particular behave
this way. For example, hydrogen ethanoate ionizes partially and some of
hydrogen ethanoate remain as molecules:
CH3COOH (aq) ↔ CH3COO-
(aq) + H+ (aq)
It is quite
easy to grasp the concept that strong acids and bases ionize more easily.
However, how do ions such as the hydrogen ion (H+) and hydroxide ion
(OH-) conduct electricity. I would like to find out more.
Lesson 3: pH Changes
Here we
performed a down-sized form of titration on hydrochloric acid using sodium
hydroxide. The concentration of both hydrochloric acid and sodium hydroxide is
0.1M or 0.1mole/litre. I read that one mole is about 6 × 1023 molecules.
Another experiment was performed: copper (II) oxide was added in access to
hydrochloric acid. This time, an interesting observation was made. The pH
increased till pH 7 where no increased was observed no matter how much copper
(II) oxide was added. Later, I learned that copper (II) oxide is not soluble in
water and thus is not an alkali. It does not release hydroxide ions. However,
it does “absorb” H+ ions by reacting to form water.
Lesson 4: When Dilute Acid Meets Metals…
Finally
after all of the basics, comes the most interesting part – chemical reactions. We
know that acids react with metals (metals which are more reactive than
hydrogen) to form a salt and hydrogen gas. But how does it work? This is
basically a Redox reaction. A Redox reaction is also known as an
oxidation-reduction reaction. Oxidation is the loss of electrons by a substance
while reduction is a gain of electrons by a substance. A Redox reaction
basically has both happening at the same time. For example, hydrochloric acid
reacts with magnesium metal to form magnesium chloride and hydrogen gas.
Firstly, we
can express the reaction in a chemical equation:
2HCl (aq) + Mg (s) à MgCl2 (aq) + H2
Then, we
convert it into an ionic equation (Cl- ions are omitted because they
do not change in their oxidation state):
Mg (s) + 2H+ (aq) à Mg2+ (aq) + H2 (g)
In the
reaction, magnesium loses its electrons and thus is oxidized:
Mg à Mg2+ + 2e-
Hydrogen
gains electrons and is oxidized:
2H+ + 2e- à H2
The next
interesting part is with the testing of hydrogen gas. Place a burning splint
(yes burning and not just lighted) into the test-tube containing the gas. If
the flame is extinguished with a ‘pop’ sound, the gas is hydrogen gas. The
reason is because when hydrogen gas mixes with oxygen gas found in the
atmosphere, it forms an explosive mixture. The burning splint ignites the
explosive mixture and the shockwave from the explosion puts out the flame. At
the same time, one hears the ‘pop’ sound.
Finally, the
last interesting part is about why copper does not react with acids. What I was
told was that copper is less reactive than hydrogen, that is copper is “not
willing” to “take over” the chloride ions from hydrochloric acid. But I am a
little unsure if we use a more concentrated acid like 4mol/dm3. I
have read that in the past, alchemists used aqua
regia or ‘royal water’ (which is in fact a mixture of concentrated
hydrochloric acid and nitric acid) to dissolve gold. And we all know gold is
even less reactive than copper.
Lesson 5: When Dilute Acid Meets Carbonates…
In this
lesson, we perform one of the oldest science experiments – the volcano. I
recall that when I was young, I mixed vinegar and baking soda together to
produce a messy fizz. Today, I know the vinegar is a kind of acid – ethanoic
acid – and baking soda is actually sodium hydrogen carbonate. Below is their
reaction:
CH3COOH (aq) + NaHCO3
(aq) à CH3COONa (aq) + H2O (l)
+ CO2 (g)
Lesson 6: When Acid Meets Alkali…
I find this
one of the more boring experiments as there isn’t much reaction happening – no
effervescence, no precipitation and no colour change. In fact, not many of the
ions change during neutralization:
H+ (aq) + OH- (aq) à H2O (l)
However, no
matter how pathetic it looks, it is the basis of a more complex volumetric
analysis. Titration. I believe that everything we learn today is in preparation
of what we would be learning tomorrow. That is why I always learn the most I
can every day.
Lesson 7: When Alkali Meets Ammonium Salts…
This
experiment is in fact somewhat similar to that of adding acid to carbonate
salts. Both of these reactions liberate a gas – one of them is acidic and the
other is alkaline. Both the gases form weak acids/alkalis as both gases prefer
to remain as covalent compounds instead of forming ionic compounds. It seems
that these two reactions are quite similar. In fact, I am considering a kind of
salt – ammonium carbonate. Water is an amphoteric substance (it behaves both
like an acid and an alkali) and when mixed with ammonium carbonate, will it
liberate carbon dioxide and ammonia gas? Below is the possible equation:
H2O (l) + (NH4)2CO3
(aq) à 2H2O (l) + 2NH3 (g) + CO2
(g)
Then again,
this could just be my imagination running wide.
Lesson 8: Preparation of Soluble and Insoluble
Salts
These two
methods use the idea of filtration either to remove the insoluble reactant or
to extract the insoluble product. The first method works when the reactant
(metal, metal oxide and metal carbonate) is insoluble. The second method works
when the salt produced is insoluble. However, what happens if both the
reactants and salts are soluble? Then we need to use titration to determine the
end point or such that both reactants are used up completely and not leftover.
For example, what if we want to prepare sodium nitrate? We know that we need
sodium cations and nitrate anions. The sodium cations can come from sodium
hydroxide while the nitrate anions can come from nitric acid. Below is the
reaction:
NaOH (aq) + HNO3 (aq) à NaNO3 (aq) + H2O (l)
At the end
point of titration, sodium hydroxide and nitric acid would have been completely
used up leaving only sodium nitrate solution left, which can be obtained
through crystallization. Salts are very useful substances. Salts such as sodium
chloride can be obtained from the sea easily. However, not all salts are
available in nature. For such salts, we need to prepare them ourselves.
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