Module 6 Flashcards

1
Q

Important acids to know:
6.1.1 Investigate the correct IUPAC nomenclature and properties of common inorganic acids and bases

A

Hydrochloric acid: HCl
Nitric acid: HNO3
Ethanoic (acetic) acid: CH3COOH
Sulfuric acid: H2SO4
Carbonic acid: H2CO3
Phosphoric acid: H3PO4
Citric Acid: C6H8O7

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2
Q

Important bases to know:
6.1.1 Investigate the correct IUPAC nomenclature and properties of common inorganic acids and bases

A

Sodium hydroxide: NaOH
Ammonia: NH3
Potassium hydroxide: KOH
Calcium hydroxide: Ca(OH)2
Magnesium hydroxide: Mg(OH)2
Sodium carbonate: Na2CO3

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3
Q

How to name organic acids
Acids with oxyanions
Oxyanions with the central atom being in a reduced state
6.1.1 Investigate the correct IUPAC nomenclature and properties of common inorganic acids and bases

A

If in aqueous form, drop the ide at the end for the anion and change it to ic and then add acid to the end. The word hydrogen changes to hydro as a prefix.
E.g. Hydrochloric acid or HF (hydrofluoric acid)

If it ends with ate, it is dropped and changed to ic. The hydrogen isn’t included in the name.
H2SO4: sulfuric acid

The suffix ite is dropped with ous.
H2SO3: sulfurous acid
HNO2: nitrous acid

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4
Q

Properties of acids and bases
6.1.1 Investigate the correct IUPAC nomenclature and properties of common inorganic acids and bases

A

Acid:
Sour taste
Can burn skin (corrosive)
Conductive in solution
Turn blue litmus red
pH<7
Base:
Bitter taste
Soapy feel in aqueous solution
Can burn skin (caustic)
Conductive in solution
Turn red litmus blue
pH.7

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5
Q

Acid + base reaction
Acid + carbonate reaction
Acid + metal reaction
6.1.1 Investigate the correct IUPAC nomenclature and properties of common inorganic acids and bases

A

Acid + base -> salt + water
Acid + carbonate ->salt + water + carbon dioxide
Acid + metal -> salt + hydrogen
Note: name of salt is cation base and anion acid

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6
Q

Define indicator
Examples of indicators and their characteristics range
6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Substances which change colour based on the pH of the environment
Indicator. pH Acidic range Transition range Basic range
transition
range
Methyl 3-4 Red (M<3.1) Orange (3.1<M<4.4). Yellow (M>4.4)
orange
Bromothymol. 6-7.5 Yellow (B<6). Green (6<B<7.6) Blue (B>7.6)
blue
Litmus. 5.5-8 Red. Purple Blue
Phenolphthalein. 8-10. Colourless. Pale pink Pink/magenta

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7
Q

Example of natural indicator and how it functions
6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Red cabbage contains weak acids called anthocyanins. Acids change colour based on the no of removable protons that remain attached to the molecule. For a diprotic anthocyanin molecule:
H2Antho(aq)⇌ H+(aq) + HAntho-(aq)
red. blue
HAntho-(aq)⇌ H+(aq) + Antho2-(aq)
blue yellow
According to LCP, as [H+] changes, the eq will shift. This will elicit a colour change hence acting as a pH indicator.
When an acid is added, the [H+] increases and the eq shifts left towards H2Antho. Thus, as the environment becomes more acidic, the colour tends to approach the rend end of the spectrum.
Conversely, when a base is added, the [OH-] increases and consumes free H+ causing [H+] to decrease. By LCP, the eq shifts right producing more Antho2-. This causes the colour to approach the yellow end of the spectrum as the environment becomes more alkaline.
Note: many acid-base indicators are also weak acids and function like this

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8
Q

Compare a natural indicator to a universal indicator and justify its use
6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

The red cabbage indicator is successfully able to classify substances into pH ranges based on colour changes, and hence fulfils the essential function of an indicator. However, it is less precise in identifying a specific pH for an approximately neutral substance in comparison to universal indicator (UI). For instance, the pH 4-7, the red cabbage indicator shows various shades of purple which are difficult to distinguish whilst UI moves through a number of more distinctive colour changes. However, red cabbage indicator can be better for substances with pH <3 or pH>11 but these substances are less common. Thus, red cabbage indicator is most likely to be useful in broadly categorising substances as acidic, basic or approximately neutral but less useful in comparing substances with marginally different pH values.

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9
Q

Indicator vs pH probe
6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Indicators pH probe
Accuracy: Relatively broad pH range Specific pH usually to 2dp
Reliability: Inter-trial variability due to colour. Highly reproducible measurements
range interpretation
Inter-investigator variability (changing person)
Validity: Destructive (1) Non-destructive
Not ideal for coloured solutions (2) Valid for all aqueous settings
Adding too much indicator changes pH (3)
Other: Cheap and portable Expensive and less portable
No maintenance Very susceptible to environment, requires calibration with
buffer solutions (4) and storage in electrolyte (5)

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10
Q

Compare indicators and pH probe through these questions
How are indicators destructive
Why aren’t indicators not ideal for coloured solutions
How do indicators affect pH
Importance of buffer solutions
How is it stored

6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

1: Indicators are destructive as they contaminate the sample solution whilst pH probes don’t
2. Acid-base indicators aren’t ideal for coloured solutions as their colour can interfere with interpretation. Excludes if coloured solutions are diluted such that the colour is sufficiently faint.
3. Indicators are themselves weak acids or bases so only few drops should be added
4. Buffer solutions are solutions with stable pH. Usually, three buffer solutions are used with stable pHs of 4, 7 and 10 to calibrate the pH probe before use.
5. pH probes should be stored in a solution of KCl to maintain the internal electrodes. They must never be stored dry as this will cause the internal electrode to degrade.

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11
Q

Why do oxides of non-metal elements (C, N, S) tend to be acidic. GIve 4 examples

6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Since they form acids when reacted with water
Co2(g) + H2O(l) ⇌H2CO3(aq) carbonic acid
2NO2(g) + H2O(l) ⇌HNO2(aq) + HNO3(aq) nitrous acid and nitric acid
SO2(g) + H2O(l) ⇌H2SO3(aq) sulfurous acid
SO3(g) + H2O(l) ⇌H2SO4(aq) sulfuric acid

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12
Q

Why do oxides of metal elements (Na, K, Ca) tend to be basic

6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Since they form hydroxide bases when reacted with water
Na2O(s) + H2O(l)⇌2NaOH(aq) sodium hydroxide
K2O(s) + H2O(l) ⇌wKOH(aq) potassium hydroxide
CaO(s) + H2O(l) ⇌Ca(OH)2 (aq) calcium hydroxide

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13
Q

`Equations of
CO2(g) + NaOH (aq)
H3PO4(aq) + CaO(s)
SO2(g) + K2O

6.1.1 Conduct an investigation to demonstrate the preparation and use of indicators as illustrators of the characteristics and properties of acids and bases and their reversible reactions

A

Acid-base reactions can be written using acidic or basic oxides as one or both reagents. The products are salt and water or simply salt. When an acidic oxide reacts with a base, the anion of the product salt is derived from the aqueous acid that the acidic oxide forms if it were reacted with water
CO2(g) + NaOH (aq) ⇌2Na2CO3(aq) + H2O(l)
H3PO4(aq) + CaO(s) ⇌2Ca3(PO4)2 (s) + 3H2O(l)
SO2(g) + K2O (s)⇌2 K2SO3(s) as reactant states are gas and solid meaning water cannot exist

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14
Q

State Lavosier’s theory. Give an example that works and doesn’t. Assess limitations and strengths
State Davy’s theory. Give an example that works and doesn’t. Assess limitations and strengths

6.16 Explore the changes in definitions and models of an acid and a base over time to explain the limitations of each model, including but not limited to:
Arrhenius theory
Brønsted-Lowry

A

Acids were substances which contained oxygen such as HNO3.
Pros: Raised need to define acids and bases
Cons: Was wrong CaO is basic.
Acids are substances which contained replaceable hydrogen meaning hydrogen in the compound could be partially or totally removed. Ca(s) + 2HCl (aq) –> CaCl2(aq) + H2(g)
Pros: Worked for many common acids
Cons: Couldn’t explain acidic or basic oxides such as SO2

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15
Q

State Arrhenius theory. Assess limitations and strengths

6.16 Explore the changes in definitions and models of an acid and a base over time to explain the limitations of each model, including but not limited to:
Arrhenius theory
Brønsted-Lowry

A

Acids are substances which in aqueous solution ionised to form H+ ions.
HA(aq) –> H+(aq) + A-(aq)
Bases are substances which in aqueous solution disassociate to form OH- ions.
XOH(aq) –> X+(aq) + OH-(aq)
Pros:
Works for most bases and acids.
Has a common fundamental mechanism of acid-base neutralisation reactions.
Able to explain potency differences between strong and weak acids by relating it to the degree of ionisation
Limitations:
Doesn’t recognise role of solvent in the relative weakness or strength of an acid where this arises from its nature and the solvent. HCl is a strong acid in water and weak in other solvents such as diethyl ether.
Many metal oxides and carbonates are basic but don’t have OH nor do they liberate OH- in aqueous solution.
Only accounted for acid-base neutralisation reactions in ionised form. Some don’t occur in this form e.g. HCl(g) + NH3(g) –> NH4Cl(s) can occur dissolved in benzene or in gaseous phase with molecular rather than ionised reactants

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16
Q

State Brønsted-Lowry theory. Assess limitations and strengths

6.16 Explore the changes in definitions and models of an acid and a base over time to explain the limitations of each model, including but not limited to:
Arrhenius theory
Brønsted-Lowry

A

Acids are substances that tend to donate protons (H+). In aqueous solutions, the acid donates a proton to a water molecule, forming the hydronium ion (H3O+). Therefore, acidity can be shown through hydronium ion formation rather than the release of hydrogen ions.
Arrhenius: CH3COOH(aq)⇌CH3COO-(aq) + H+(aq)
Brønsted-Lowry: CH3COOH(aq) + H2O(l)⇌CH3COO-(aq) + H3O+(aq)
A base is defined as a substance which tends to accept protons
NH3(aq) + H2O(l) ⇌NH4+(aq) + OH-(aq)
Acid-base reactions are generalised as an exothermic proton transfer reaction where the acid donates a proton to a base which accepts the proton.
Pros:
Works for the behaviour of acid, bases and their reactions in non-aqueous solvents.
Considers the role of the solvent in determining acid weakness or strength
Explains existence of amphiprotic substances
HCl(aq) + H2O(l) –> H3O+(aq) + Cl-(aq)
HCl: acting as acid. H2O: acting as base
NH3(aq) + H2O(l) –> NH4+(aq) + OH-(aq)
NH3: acting as base. H2O: acting as acid
Cons:
Cannot explain amphoteric substances that aren’t amphiprotic
BF3(g) + NH3(g) –> BF3NH3(g)
Cannot explain bases and acids that don’t accept/donate protons

17
Q

Amphoteric vs Amphiprotic substances

6.16 Explore the changes in definitions and models of an acid and a base over time to explain the limitations of each model, including but not limited to:
Arrhenius theory
Brønsted-Lowry

A

Amphoteric: Can act as acid or base such as Al(OH)3 and PbO.
Amphiprotic: substance which can act as acid or base specifically due to its ability to either donate or accept protons in different chemical environments such as H2O, HSO4-, H2PO4-, HPO42-, HCO3-
All amphiprotic substances are amphoteric but no vice versa.

18
Q

What are protic substances
State the acid types

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Protic substances have the capacity to act as a proton donor.
Monoprotic: HCl, HNO3, HF, CH3COOH
Diprotic: H2CO3, H2SO4
Triprotic: H3PO4, C6H8O7
Acids donating 2+ protons ionise stepwise:
H2SO4 first ionisation: H2SO4(aq) + H2O(l) –> HSO4-(aq) + H3O+(aq)
Second ionisation: HSO4-(aq) + H2O(l)⇌So42-(aq) + H3O+(aq)
H3PO4 first ionisation: H3PO4(aq) + H2O(l)⇌H2PO4-(aq) + H3O+(aq)
Second ionisation: H2PO4-(aq) + H2O(l)⇌HPO42-(aq) + H3O +(aq)
Third ionisation: HPO42-(aq) + H2O(l)⇌PO43-(aq) + H3O(aq)

19
Q

What is a strong acid

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

A strong acid in water will completely ionise to form hydronium ions (degree of ionisation=100%)
HCl(aq) + H2O(l) –> Cl-(aq) + H3O+(aq)
HNO3(aq) + H2O(l) –> NO3-(aq) + H3O+(aq)
A unidirectional arrow represents the fact it goes to completion
A weak acid doesn’t completely ionise in an aqueous solution to form hydronium ions. If degree of ionisation<100%, it is a weak acid.
CH3COOH(aq) + H2O(l) ⇌CH3COO-(aq) + H3O+(aq)
H3PO4(aq) + H2O(l)⇌H2PO4-(aq) + H3O+(aq)
For weak acids, reversible arrow is used

20
Q

What acids are strong or weak relative to water

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Strong relative to water: HCl, HBr, HI, HNO3, H2SO4 (only first ionisation is strong, 2nd is weak)
Weak relative to water: HF, CH3COOH, H2CO3, H3PO4, C6H8O7
Between D and C is strong in solvent
Wants to accept protons more<——————————————————————>wants to donate protons more
A B C D E

21
Q

Define acid strength in Brønsted-Lowry theory

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Acid strength is defined as its ability to donate a proton to X. This strength depends on the Brønsted-Lowry basic properties of the other species X which may be the solvent and/or reactant. For example, sulfuric acid is a strong acid relative to water (first ionisation). However, it is weak relative to acetic acid as it reversibly protonates. However, it is stronger than acetic acid as it can protonate the latter whilst the reverse cannot happen. If an acid is deemed strong or weak without reference, assume water is the solvent.

22
Q

Explain whether H2O or HCO3- is a stronger acid

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

IN the presence of H2O(l), HCO3- behaves mainly as a brønsted-lowry base, accepting a proton from water. HCO3-(aq) + H2O(l) ⇌H2CO3(aq) + OH-(aq)
Therefore, HCO3- is a stronger base than H2O . Or can explain in context of acid.

23
Q

What are conjugate acid/base pairs
State their relative strengths

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Conjugate base: acid donates a proton forming this
Conjugate acid: base accepts a proton becoming this
HA(aq) + H2O(l)⇌H3O+(aq) +A-(aq)
HA: brønsted-lowry acid
A-: conjugate base
H2O: brønsted-lowry base
H3O+: conjugate acid

Conjugate base of WA tends to be WB
Conjugate base of WB tends to be WA
Conjugate acid of a SA is extremely weak/almost neutral
Conjugate of a SB is extremely weak/almost neutral
Remember: subsequent ionisations of multiprotic acids are much weaker i.e. triprotic weak acid produces less H3O+ than monoprotic strong acid

24
Q

How to demonstrate a species is amphiprotic

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Write one equation with a strong base and another equation with a strong acid. In the presence of a strong base (OH-, NaOH, OH), an amphiprotic substance will behave as a Brønsted-Lowry acid. In the presence of a strong acid (H3O+, HCl, HNO3), an amphiprotic substance will behave as a Bronsted-Lowry base. H2PO4- behaves as a WA in water but is a stronger acid relative to water.
Net ionic equation
H2PO4-(aq) + OH-(aq)–>HPO42-(aq) + H2O(l) acid
H2PO4-(aq) + H3O+(aq) –>H3PO4(aq) + H2O(l) base
Full equation
KH2PO4-(aq) + KOH-(aq)–>K2HPO42-(aq) + H2O(l) acid
KH2PO4-(aq) +KHCl+(aq) –>H3PO4(aq) + KCl (l) base

25
Q

What is a neutralisation reaction

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Neutralisation reactions are an acid-base reaction that usually go to completion and don’t produce H3O+ or OH- (if in aqueous solvent). Reactions with neutral solvents are not neutralisation reactions rather acid-base reactions. Neutralisation reactions don’t have protonated or deprotonated solvent molecules as products. The salt of neutralisation may undergo eq reactions with the solvent to produce H3O+ or OH- (if aqueous) meaning the final solution after neutralisation doesn’t need to be neutral. E.g.
CH3COOH(aq) + NaOH (aq) –> NaCH3COO (aq) + H2O(l) produces a basic salt (NaCH3COO)

26
Q

Cause of neutralisation either going to completion or not

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

Consider CH3COOH(aq) + NaOH(aq) –>NaCH3COO(aq) + H2O(l)
WA vs SB
Using LCP, since CH3COOH(aq) is a weak acid in water, it forms an eq:
Ch3COOH(aq) + H2O(l)⇌CH3COO-(aq) + H3O+(aq)
When hydroxide ions are added, they consume the free H3O+(aq). This reduces [H3O+] and the system shifts right to increase [H3O+] by LCP. As further NaOH (aq) is added , more H3O+ is consumed and the eq constant continues shifting right. Eventually all the CH3COOH is consumed. Hence, a weak monoprotic acid requires the same amount of SB to completely neutralise. Works for strong monoprotic acid as well.

Using Bronsted-lowry
Acetic acid is a weak acid relative to water, but it is a SA relative to NaOH. This is because NaOH is already a SB relative to water and acetic acid is a stronger acid than water. Hence, acetic acid will ionise to completion in the presence of NaOH so the neutralisation reaction is complete.

27
Q

What is the degree of ionisation

6.2.4 Write Ionic Equations to represent the disassociation of acids and bases in water, conjugate acid/base pairs in solution and amphiprotic nature of some salts for example
Sodium hydrogen carbonate
Potassium dihydrogen phosphate

A

In water, aren’t always equivalent with acid HA: deg of ionisation= [H3O+]eq/[HA]initial x 100% OR [A-]/[HA]initial x 100%
Is the ratio of ionised acid molecules to the initial number of acid molecules. [H3O+] or [A-] at eq are surrogates for HA that has ionised. Varies depending on acid concentration and other equilibrium disturbances (temp).

28
Q

How does the degree of ionisation change in HA(aq) + H2O(l)⇌A-(aq) + H3O+(aq). ΔH<0

A

Disturbance Effect on deg of ion Formula used Effect on Ka
Add A-(NaA) Decreases. [A-] ↑ –> shift left (LCP). ↓ [H3O+]eq. [H3O+]eq/[HA] initial. No change
Add H3O+ (HCl). Decreases. [H3O+] ↑ –> shift left (LCP). ↓ [A-]eq. [A-]eq/[HA] initial. No change
Finish it off pg 18