9701/23 · May/June 2026
Download PDFThe chlorides of Period 3 elements show different physical and chemical properties.
Complete Table 1.1. Table 1.1
| element | formula of chloride | type of bonding in the chloride | type of reaction, if any, of the chloride with cold water |
| sodium | |||
| silicon |
Write an equation for the reaction of with an excess of cold water.
The reaction of chlorine with cold water is used in water purification. Write an equation for the reaction of chlorine with cold water.
Explain the use of chlorine in water purification.
The relative strength of , and as oxidising agents can be compared by adding to separate samples of and . Describe the relative reactivity of , and as oxidising agents.
Complete Table 1.2 to describe the reactions of with separate samples of and . Table 1.2
| aqueous halogen | colour of aqueous halogen | appearance after is added | halide ions present in the mixture after the reaction |
| pale green | |||
| red–brown |
Describe what is observed when , followed by , are added to a sample of . observation after addition of ........................................................................................ observation after addition of .......................................................................................
Group 18 elements exist as colourless gases at room temperature and pressure. Table 2.1
| atom | relative volume of atom |
| neon | 172 |
| argon | 287 |
| krypton | 355 |
| xenon | 446 |
Use Table 2.1 to describe and explain the variation in atomic radius down Group 18.
Identify one Group 18 element from Table 2.1 that behaves most like an ideal gas under standard conditions. Explain your answer.
A sample of of gas occupies at and . Calculate the relative molecular mass, , of assuming that behaves as an ideal gas. of .........................................................
The conditions used for the conversion of sulfur dioxide to sulfur trioxide in the Contact process are carefully controlled. reaction 1

Complete Figure 3.1 to show the reaction pathway diagram for reaction 1. Draw arrows to represent the enthalpy change, , and activation energy, .
Define Le Chatelier's principle.
In industry, reaction 1 occurs at and with a catalyst. Complete Table 3.1 by using the terms 'increase', 'decrease' or 'no change'. Table 3.1
| use temperature greater than | without catalyst | |
| effect on value of equilibrium constant, | ||
| effect on yield of product at equilibrium | ||
| effect on rate of reaction |
A sealed tube that initially contains only of and of is left to reach equilibrium. At equilibrium, of is present and the total pressure is . reaction 1 Complete Table 3.2. Table 3.2
| amount initially/mol | 2.00 | 2.00 | 0 |
| amount at equilibrium/mol | 1.96 | ||
| mole fraction at equilibrium | 0.01325 | 0.3377 |
Table 3.3 shows the mole fractions at equilibrium of , and under different conditions. Table 3.3
| mole fraction at equilibrium | 0.360 | 0.019 | 0.621 |
Calculate at using the data from Table 3.3. Include units in your answer. ............................................................... units ...............................................................
The structure of compound is shown in Figure 4.1. Figure 4.1




Complete Table 4.1. Table 4.1
| primary hydroxyl groups | secondary hydroxyl groups | tertiary hydroxyl groups | |
| number of groups in one molecule of |
Complete Table 4.2 to show what is observed when separate samples of are added to each reagent. State 'none' if no reaction occurs. Table 4.2
| reagent | observation with |
| 2,4-dinitrophenylhydrazine (2,4-DNPH) | |
| Fehling's reagent | none |
Suggest why Fehling's reagent does not react with but does react with aldehyde functional groups.
Figure 4.1 is repeated for use in 4(b). is completely oxidised by heating under reflux with an excess of acidified to produce organic compound . Describe the colour change in this reaction. colour of mixture at start of the reaction ............................................................................ colour of mixture after the reaction ....................................................................................
Draw the structure of .
Compounds , and are structural isomers of . Describe structural isomerism.
Identify which of structures , , and show stereoisomerism. Explain your answer by referring to the relevant parts of the molecule that cause stereoisomerism.
reacts with reagent to produce compound . Name reagent .
Exactly of one of the isomers, , , or , is completely oxidised by of acidified to produce only one organic compound with molecular formula . Identify which isomer, , , or , is used in this reaction.
Complete the equation for this reaction.
Propane, , reacts with in the presence of ultraviolet light to produce different organic products, including those shown in Table 5.1. Table 5.1
| structure of product | systematic name of product |
| 1-chloropropane | |
| 2-chloropropane | |
| 2,3-dimethylbutane | |
| hexane | |
| 2-methylpentane |



Complete Table 5.1.
Name the mechanism for the reaction of propane and in the presence of ultraviolet light.
The mechanism for this reaction involves three stages. stage 1 initiation stage 2 propagation stage 3 termination During the initiation reaction, a chlorine free radical is produced. Complete Figure 5.1 to describe the arrangement of electrons in a chlorine free radical.
Suggest a reaction sequence of two propagation reactions that result in forming . propagation reaction 1 ............................................. ................................................................. propagation reaction 2 ................................................................... ........................................
Suggest a reaction sequence of one propagation reaction followed by a termination reaction that results in forming . propagation reaction 3 ......................................... ..................................................................... termination reaction ...............................................................
Compound has the molecular formula . Figure 5.2 shows the mass spectrum of . Explain the difference in relative abundance of the peaks at and .
Complete Table 5.2. Table 5.2
| value of peak | molecular formula of species responsible for peak |
| 84 | |
| 86 | |
| 88 |






