Organic Synthesis - exam practice
Organic Synthesis
Question 1 of 15
1 of 15
Which pair of compounds can bothbe separately hydrolysed in acidic conditions to form propanoic acid?
Question 2 of 15
2 of 15
Which set of reagents is not suitable for the step indicated?

Question 3 of 15
3 of 15
Which reaction may be used to make a carboxylic acid in a single step?
Question 4 of 15
4 of 15
Energy is released in the human body by the oxidation of glucose in a complex sequence of reactions. Part of this sequence is the Krebs cycle.
One reaction in the Krebs cycle is the conversion of fumaric acid into malic acid.
HO2CCH=CHCO2H ➔ HO2CCH(OH)CH2CO2H
fumaric acid malic acid
Which reagents could achieve this transformation in the laboratory?
Question 5 of 15
5 of 15
The compound ‘leaf alcohol’ is partly responsible for the smell of new-mown grass.
CH3CH2CH=CHCH2CH2OH
leaf alcohol
What will be formed when ‘leaf alcohol’ is oxidised using an excess of hot, acidified K2Cr2O7(aq)?
Question 6 of 15
6 of 15
Which pair of reagents will take part in a redox reaction?
Question 7 of 15
7 of 15
Which reaction would not give ethanoic acid?
Question 8 of 15
8 of 15
Which compound could be formed by a one-step reaction from 1-chloropropane?
Question 9 of 15
9 of 15
Which statement about the reactions of methanol is correct?
Question 10 of 15
10 of 15
Which statement about the purification of a solid by recrystallisation is correct?
Question 11 of 15
11 of 15
Which substance cannotbe made in a single step from C2H4?
Question 12 of 15
12 of 15
Which of these reagent(s) will not react with HOCH2CH2CH2COOH?
Question 13 of 15
13 of 15
Which one of the following reacts with ethanoic acid andwith phenol?
Question 14 of 15
14 of 15
Which compound does not react with nucleophiles?
Question 15 of 15
15 of 15
Which is the mechanism for this conversion?
