2.1 Simple equilibria and acid-base reactions Flashcards

1
Q

heating of hydrated copper(II) sulfate, CuSO4⋅5H2O

A

Heating blue hydrated copper(II) sulfate crystals causes a colour change to white anhydrous copper(II) sulfate.

This is an endothermic process.

Water is released and instantly turns to steam due to the heat.

Some of the steam condenses on the cooler parts of the boiling tube.

Adding water to white anhydrous copper(II) sulfate turns it back to blue hydrated copper(II) sulfate.

A hissing sound is heard as some water boils from the heat of the reaction.

This is an exothermic reaction.

In a reversible reaction, if one direction is endothermic, the reverse is exothermic.

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2
Q

Dynamic equilibrium

A

is the equilibrium that exists when the rate of the forward reaction equals the rate of the reverse reaction.

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3
Q

A chemical system is in dynamic equilibrium when:

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it is dynamic at the molecular or ionic level
both forward and reverse rates are equal
it is a closed system, i.e. a system where substances cannot leave or enter
it has macroscopic properties, e.g. concentration of the reactants and the products remain the same.
The reaction is reversible

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4
Q

when does equilibrium lie to left and right

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Increasing the concentration of a reactant:
the position of equilibrium moves to the right-hand side, forming more products, e.g. more ethyl ethanoate and water
the concentrations of the additional ethanol and ethanoic acid will decrease as a result of the change.

Increasing the concentration of a product:
the position of equilibrium will move to the left-hand side, forming more reactants, e.g. more ethanol and ethanoic acid
the concentrations of the additional ester and water will decrease as a result of the change.

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5
Q

Equilibrium is a dynamic state

A

at a molecular level change is constantly taking place in both directions at equal rates. Macroscopic properties such as temperature, pressure, mass and volume are constant.

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6
Q

The position of equilibrium can be altered by changing one or more of the following in the system:

A

concentration of the reactants or products
pressure in reactions involving gases
temperature.

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7
Q

Le Chatelier’s principle.

A

When a system in dynamic equilibrium is subjected to a change, the position of equilibrium will shift to minimise the change.

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9
Q

The effect of a catalyst on equilibrium

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In a system at equilibrium, a catalyst speeds up the rate of the forward and reverse reactions equally. Therefore, a catalyst has no effect on the position of the equilibrium. It does, however, allow the state of equilibrium to be established more quickly.

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10
Q

The effect of changing the temperature on the position of equilibrium depends on the enthalpy sign (ΔH):

A

If the reaction is exothermic (ΔH is negative), increasing temperature shifts equilibrium to the left (towards the reactants).

If the reaction is endothermic (ΔH is positive), increasing temperature shifts equilibrium to the right (towards the products).

Decreasing temperature has the opposite effect:

Shifts equilibrium right for exothermic reactions.

Shifts equilibrium left for endothermic reactions.

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11
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12
Q

equilibrium equation

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13
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15
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16
Q

When Kc is large

A

If Kc is very large (Kc&raquo_space;1) the equilibrium lies to the RHS so the reaction mixture contains mostly products

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17
Q

When Kc is small

A

If Kc is very small (Kc &laquo_space;1) the equilibrium lies to the LHS so the reaction mixture contains mostly reactants

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18
Q

Kc close to 1

A

If Kc is close to 1 the mixture contains a similar concentration of both reactant and products

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19
Q

When stating the value for Kc for a particular reaction, it is important to indicate the equation on which the constant is based.

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20
Q

The units for Kc depend upon the number of reactants and products and their stoichiometric quantities. For this general example given in the first equation above:

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21
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22
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23
Q

Calculate the Kc value for experiments 2 – 4 from the table on the previous screen. Is Kc constant?

24
Q

Acid

A

something that produces an excess of H+ ions in an aqueous solution.

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Alkali
something that produces an excess of OH- ions in an aqueous solution.
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Brønsted-Lowry (B-L) definition acid
Acid: donates a proton during chemical reactions: In the first example, water is the base as it accepts a proton from the hydrogen chloride.
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Brønsted-Lowry (B-L) definition base
Base: accepts a proton during chemical reactions; a base is called an alkali if it dissolves in water: In the second example, water acts as an acid donating a proton to the ammonia. Compounds or molecules that can act as both an acid and a base are called amphoteric.
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strong acid
will dissociate fully (100%).
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eg strong acids
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weak acid
only partially dissociates
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eg of weak acid
citric acid and ethanoic acid
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Acids undergo neutralisation reactions with
bases, alkalis and carbonates
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acids + alkalis eg nitric acid and sodium hydroxide full equation, ions present, ionic equation
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acids + carbonates eg sulfuric acid + sodium carbonate full equation, ions present, ionic equation
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acids + metals eg hydrocholric acid and magnesium full equation, ions present, ionic equation
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pH equation, log
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Calculating pH
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primary standard
a solid eg Anhydrous sodium carbonate (Na₂CO₃) primary standard is a very pure chemical used to make a standard solution (a solution of known concentration). ✅ Must be: Very pure Stable (doesn’t react or break down easily) Not hygroscopic (doesn’t absorb water from the air) High Mr (to reduce weighing errors) 🧪 You weigh it accurately, then dissolve in a known volume of water to make a solution with a precise concentration.
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how to make a standard solution
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titration - to determine conc of an acid
The first step is to fill the burette, usually with the acid. Use a small funnel, making sure that the tip of the burette is filled. Remove the funnel after filling and read the level of the acid. Then proceed as follows: A. Use a pipette to add a measured volume (usually 25.0 cm3) of the other solution, in this case the alkali, to a conical flask. B. Add a few drops of indicator to the solution in the conical flask. C. Run acid from the burette to the solution in the flask, swirling as you do so. Stop when the indicator turns colour. This will be your ‘rough’ titration and you know that this is the maximum volume you need to add from the burette. D. Repeat the titration, this time adding the acid dropwise when you near the volume you got in part C, until the indicator just turns colour. This is the endpoint of your titration. Record the volume of acid used (the titre). Repeat until you have at least two readings that are within 0.20 cm3 (called concordant results) of each other and calculate a mean titre.
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acid base titration worked eg of calculating conc of standard solution
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🧪 Back Titration – Key Concept
In a back titration, an excess known amount of a reagent is added to a substance to ensure complete reaction. The unreacted excess is then titrated to determine how much was left over, and from this, you can calculate how much was used in the original reaction.
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eg of back titration and why it was used
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🧪 Double Titration – Concept
A double titration is used when a solution contains two different bases (often of differing strengths, like a strong base and a weak base), and we want to determine the concentration of each base individually. This method takes advantage of the fact that: Different acid-base indicators change colour at different pH values. This allows each base to be quantified separately by selecting the appropriate indicator for each one.
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Double Titration - How it works
Stage 1: Titration of Strong Base A strong acid is added to the solution containing both bases. The first indicator is chosen to change colour at a low pH (e.g. methyl orange), suitable for identifying the end-point of the strong base. At this point, only the strong base has reacted completely with the acid. Stage 2: Titration of Weak Base More acid is added to react with the remaining weak base. A second indicator is used (e.g. phenolphthalein) that changes colour at a higher pH, appropriate for detecting the end-point of the weak base. Now, both the strong and weak bases have reacted, and the titration is complete.
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🧠 Purpose and Application Double titration
From the volume of acid added in each stage: You can calculate the moles of acid reacting with each base. Using stoichiometry, determine the concentration of both bases in the original mixture.
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✅ Key Exam Tips Double titration
Know the pH range of indicators: Methyl orange: ~3.1–4.4 (red to yellow) → good for strong base–strong acid Phenolphthalein: ~8.3–10 (colourless to pink) → good for weak base–strong acid State clearly that the first base neutralised is the stronger base, due to the indicator used. Show separate balanced equations if needed for each reaction.
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🧪 Determining Concentrations of NaOH and Na₂CO₃ via Double Titration
A mixture of NaOH (sodium hydroxide) and Na₂CO₃ (sodium carbonate) can be analysed using a double titration with HCl (hydrochloric acid). Two indicators are used at different pH ranges: Phenolphthalein (changes from pink to colourless at pH ~9) – used in the first titration. Methyl orange (changes from yellow to red/orange at pH ~4) – used in the second titration. 🔁 Stage 1 – Phenolphthalein Titration (Strong base + half carbonate) Reactions during this stage: NaOH + HCl → NaCl + H₂O Na₂CO₃ + HCl → NaHCO₃ + NaCl End point (pH ~9): All NaOH and half of the Na₂CO₃ have reacted. 🔁 Stage 2 – Methyl Orange Titration (Remaining carbonate) Reaction: NaHCO₃ + HCl → NaCl + CO₂ + H₂O The second titre gives the moles of NaHCO₃, which is equal to the moles of Na₂CO₃ (since all Na₂CO₃ becomes NaHCO₃ in stage 1). ➗ Calculations Summary Moles of Na₂CO₃ = moles of HCl from second titre. Moles of NaOH = moles of HCl from first titre − moles of Na₂CO₃. Use the moles and volumes to calculate concentrations of NaOH and Na₂CO₃ in the original mixture.
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