IBDP Chemistry -Reactivity 2.2 How fast? The rate of chemical change - IB Style Questions For SL Paper 2 -FA 2025
Question
Bromine, \(Br_2(l)\), and methanoic acid, \(HCOOH(aq)\), react in the presence of sulfuric acid.
\[ Br_2(l) + HCOOH(aq) \rightarrow 2\,HBr(aq) + CO_2(g) \]
(a) Suggest an experimental method that could be used to determine the rate of reaction.
(b) The sulfuric acid is a catalyst in this reaction. Explain how a catalyst increases the reaction rate.
(c) Methanoic acid can react with ethanol to produce an ester. Draw the full structural formula of the organic product and state its name.
Structural formula:
Name:
Structural formula:
Name:
(d) (i) Write the equation for the complete combustion of ethanol.
(ii) Determine the enthalpy change for the combustion of ethanol, in \(kJ\,mol^{-1}\), using section 11 of the data booklet.
(ii) Determine the enthalpy change for the combustion of ethanol, in \(kJ\,mol^{-1}\), using section 11 of the data booklet.
(e) Bromine also reacts with but-2-ene.
(i) Identify the type of reaction.
(ii) Predict the structural formula of the reaction product.
(iii) Draw the structure of a section of a polymer formed from three monomers of but-2-ene.
(i) Identify the type of reaction.
(ii) Predict the structural formula of the reaction product.
(iii) Draw the structure of a section of a polymer formed from three monomers of but-2-ene.
Most-appropriate topic codes (IB Chemistry 2025):
• Reactivity 2.2: How fast? The rate of chemical change — parts (a), (b)
• Structure 3.2: Functional groups: Classification of organic compounds — part (c)
• Reactivity 1.3: Energy from fuels — part (d)(i)
• Reactivity 1.2: Energy cycles in reactions — part (d)(ii)
• Reactivity 3.4: Electron-pair sharing reactions — parts (e)(i), (e)(ii)
• Structure 2.4: From models to materials — part (e)(iii)
• Structure 3.2: Functional groups: Classification of organic compounds — part (c)
• Reactivity 1.3: Energy from fuels — part (d)(i)
• Reactivity 1.2: Energy cycles in reactions — part (d)(ii)
• Reactivity 3.4: Electron-pair sharing reactions — parts (e)(i), (e)(ii)
• Structure 2.4: From models to materials — part (e)(iii)
▶️ Answer/Explanation
Detailed solution
(a)
One suitable method is to measure the volume of \(CO_2\) produced with time using a gas syringe (or a pressure sensor).
The rate can be found from \(\Delta(\text{volume of }CO_2)/\Delta t\) or from the gradient of a volume–time graph.
One suitable method is to measure the volume of \(CO_2\) produced with time using a gas syringe (or a pressure sensor).
The rate can be found from \(\Delta(\text{volume of }CO_2)/\Delta t\) or from the gradient of a volume–time graph.
(b)
A catalyst provides an alternative reaction pathway with a lower activation energy, \(E_a\).
This means a greater fraction of particles have \(E \ge E_a\) at the same temperature, so there are more successful collisions per unit time and the rate increases.
A catalyst provides an alternative reaction pathway with a lower activation energy, \(E_a\).
This means a greater fraction of particles have \(E \ge E_a\) at the same temperature, so there are more successful collisions per unit time and the rate increases.
(c)
Ester formed from methanoic acid and ethanol is ethyl methanoate.
Structural formula:
\(H{-}C(=O){-}O{-}CH_2{-}CH_3\)
Name: ethyl methanoate

Ester formed from methanoic acid and ethanol is ethyl methanoate.
Structural formula:
\(H{-}C(=O){-}O{-}CH_2{-}CH_3\)
Name: ethyl methanoate
(d)
(i)
\[ CH_3CH_2OH(l) + 3O_2(g) \rightarrow 2CO_2(g) + 3H_2O(g) \]
(ii)
Using average bond enthalpies (data booklet section 11):
Bond breaking (reactants)
In \(CH_3CH_2OH\): \(1\,C{-}C,\ 5\,C{-}H,\ 1\,C{-}O,\ 1\,O{-}H\)
In \(3O_2\): \(3\,O{=}O\)
\[ E_{\text{break}} = 1(346) + 5(414) + 1(358) + 1(463) + 3(498) \] \[ = 346 + 2070 + 358 + 463 + 1494 = 4731\ \text{kJ} \]
Bond forming (products)
In \(2CO_2\): \(4\,C{=}O\)
In \(3H_2O\): \(6\,O{-}H\)
\[ E_{\text{form}} = 4(804) + 6(463) = 3216 + 2778 = 5994\ \text{kJ} \]
\[ \Delta H \approx E_{\text{break}} – E_{\text{form}} = 4731 – 5994 = -1263\ \text{kJ mol}^{-1} \]
✅ \(\Delta H_{\text{comb}} \approx -1263\ kJ\,mol^{-1}\).
(i)
\[ CH_3CH_2OH(l) + 3O_2(g) \rightarrow 2CO_2(g) + 3H_2O(g) \]
(ii)
Using average bond enthalpies (data booklet section 11):
Bond breaking (reactants)
In \(CH_3CH_2OH\): \(1\,C{-}C,\ 5\,C{-}H,\ 1\,C{-}O,\ 1\,O{-}H\)
In \(3O_2\): \(3\,O{=}O\)
\[ E_{\text{break}} = 1(346) + 5(414) + 1(358) + 1(463) + 3(498) \] \[ = 346 + 2070 + 358 + 463 + 1494 = 4731\ \text{kJ} \]
Bond forming (products)
In \(2CO_2\): \(4\,C{=}O\)
In \(3H_2O\): \(6\,O{-}H\)
\[ E_{\text{form}} = 4(804) + 6(463) = 3216 + 2778 = 5994\ \text{kJ} \]
\[ \Delta H \approx E_{\text{break}} – E_{\text{form}} = 4731 – 5994 = -1263\ \text{kJ mol}^{-1} \]
✅ \(\Delta H_{\text{comb}} \approx -1263\ kJ\,mol^{-1}\).
(e)
(i)
This is an electrophilic addition reaction (addition of \(Br_2\) across the \(C{=}C\) double bond).
(ii)
Product is 2,3-dibromobutane:
\(CH_3CHBrCHBrCH_3\).
(iii)
A section of an addition polymer from three monomers of but-2-ene can be shown as:
\[ {-}CH(CH_3){-}CH(CH_3){-}CH(CH_3){-}CH(CH_3){-}CH(CH_3){-}CH(CH_3){-} \] (three repeating units of \(\left[{-}CH(CH_3){-}CH(CH_3){-}\right]\)).![]()
