2025 P1 Q021 Q30
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2025 P1 Q021 Q30
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2025 A Level H2 Chemistry Paper 1 Suggested Solutions - Q21 to Q30
Question 21
Answer: B
Topic: Carboxylic Acid and Derivatives
Explanation:
For each of the compounds 1 to 3, we hydrolyse the ester with sulfuric acid to form carboxylic acid and alcohol, followed by oxidation of alcohol with dichromate(VI) to form carboxylic acid. If there is only 1 organic compound product then it could be ester J.
Ester 1 will form only ethanoic acid on hydrolysis followed by oxidation.
Ester 2 will form propanoic acid and propanone as final products.
Ester 3 will form butanoic acid and ethanoic acid as final products.
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Question 22
Answer: B
Topic: Nitrogen Compounds and Polymers
Explanation:
The building blocks of proteins are alpha-amino acids where the amine group is bonded to the carbon directly bonded to acid group.
Only 2,6-diaminohexanoic acid is alpha-amino acid. The other two are beta-amino acids hence not found in proteins.
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Question 23
Answer: A
Topic: Carboxylic Acid and Derivatives
Explanation:
A is correct. Product formed is ethyl ethanamide.
B is wrong. Product formed should be phenyl ethanoate with 2 oxygen atoms instead of 1.
C is wrong. Product formed should be 1-methylethyl ethanoate instead of 1-methylethyl propanoate.
D is wrong. Product formed should be ethanoic acid instead of ethanal.
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Question 24
Answer: B
Topic: Nitrogen Compounds and Polymers
Explanation:
To compare base strengths between the 3 compounds, we focus on lone pair availability on nitrogen for donation.
Phenylamine Y is the least basic since lone pair of N is delocalised into benzene ring and less available for donation.
Z is a primary amine with 1 electron donating alkyl group which increase nitrogen's electron density and lone pair availability for donation, hence more basic than Y.
X is a secondary amine with 2 electron donating groups therefore should be more basic than Z.
Finally the base strength in increasing order should be Y, Z, X.
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Question 25
Answer: C
Topic: Organic Chemistry Synthesis
Explanation:
The synthesis routes with reagents and conditions are given so we just need to verify if the correct final product is formed for each route.
Route 2 is wrong since we start off with chloromethylbenzene to form benzoic acid but we want to form phenylethanoic acid (with an additional carbon) instead.
Route 3 is wrong since in step 3 there is no reaction between 2 alcohols to form ester.
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Question 26
Answer: C
Topic: Electrochemistry
Explanation:
The chlorine half cell should undergo reduction and silver half cell oxidation and Ecell can be calculated to be +0.56V.
On adding sodium chloride to the silver half cell, AgCl ppt is formed which lowers the Ag+ concentration. This shifts the position of equilibrium for silver half cell to the left, and E value should decrease (less than +0.8V).
Since silver half cell is the anode, a less positive E for oxidation means Ecell will increase (greater than +0.56V).
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Question 27
Answer: A
Topic: Electrochemistry
Explanation:
From the balanced equation we can deduce 6 moles of electrons are transferred between the reactants.
Using formula dG = -nFEcell we can calculate dG to be -625 kJ mol-1.
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Question 28
Answer: C
Topic: Electrochemistry
Explanation:
To be reduced by Ni, the E value for M2+/M half cell must be greater than -0.25V. Therefore answer must be Sn2+.
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Question 29
Answer: B
Topic: Electrochemistry
Explanation:
To find charge of copper ion, we need to determine mole ratio of electrons to Cu.
Mole of electrons can be determined via Faraday's equations Q = I.t = n.F
Mole of copper is its mass over atomic mass.
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Question 30
Answer: B
Topic: Transition Elements
Explanation:
Element M must be a transition metal with larger atomic mass and smaller radius than Ca. Hence M must have greater density than Ca.
MCl2 will have more exothermic lattice energy compared to CaCl2 since M2+ is smaller than Ca2+ and magnitude of lattice energy for MCl2 should be greater.
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