9701_s23_qp_23
A paper of Chemistry, 9701
Questions:
6
Year:
2023
Paper:
2
Variant:
3

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A neutralisation reaction occurs when NaOHis added to H2SO4. equation 1 2NaOH+ H2SO4Na2SO4+ 2H2ODefine enthalpy change of neutralisation, ∆Hneut . In an experiment, 50.0 cm3 of 2.00 mol dm–3 NaOHis added to 60.0 cm3 of 1.00 mol dm–3 H2SO4in a polystyrene cup and stirred. Both solutions have a temperature of 21.4 °C before mixing. The maximum temperature of the mixture is measured. Use equation 1 to calculate the amount, in mol, of H2SO4that is neutralised in the experiment. amount of H2SO4 neutralised = mol Calculate the theoretical maximum temperature of the mixture in this experiment. Assume that: • enthalpy change of neutralisation, ∆Hneut , of NaOHand H2SO4is –57.1 kJ mol–1 • full dissociation of H2SO4occurs • the specific heat capacity of the final solution is 4.18 J g–1 K–1 • 1.00 cm3 of the final solution has a mass of 1.00 g • there is no heat loss to the surroundings • the experiment takes place at constant pressure. Show your working. theoretical maximum temperature = °C The enthalpy change of neutralisation of CH3COOHand NaOHis –55.2 kJ mol–1. Complete the equation for the reaction. CH3COOH + NaOH Values for the enthalpy change of neutralisation, ∆Hneut , are shown in Table 3.1. Table 3.1 reagents ∆Hneut / kJ mol–1 NaOH + HCl –57.1 NaOH + CH3COOH –55.2 Suggest why the value for ∆Hneut of the weak acid, CH3COOH, reacting with NaOH is different to the value obtained using the strong acid, HCl. Assume that the values are determined under the same conditions.
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Compound W, CH2=CHCN, is used to make an addition polymer which is present in carbon fibres. Draw one repeat unit of the addition polymer of W. CH3CHO is used in a two-step synthetic route to form W, as shown in . In step 1, CH3CHO is heated with HCN in the presence of KCN. CH3CHO CH3CH(OH)CN CH2=CHCN step 1 step 2 W Name the mechanism for the reaction in step 1 in . Complete to show the mechanism for the reaction in step 1. Include all products, charges, dipoles, lone pairs of electrons and curly arrows, as appropriate. O H CH3 C N C Suggest a suitable reagent and conditions for step 2 in . shows the infrared spectrum of W, CH2=CHCN. wavenumber / cm–1 S T transmittance / % 50 Table 6.1 bond functional groups containing the bond characteristic infrared absorption range (in wavenumbers) / cm–1 C–O hydroxy, ester 1040–1300 C=C aromatic compound, alkene 1500–1680 C=O amide carbonyl, carboxyl ester 1640–1690 1670–1740 1710–1750 C≡N nitrile 2200–2250 C–H alkane 2850–2950 N–H amine, amide 3300–3500 O–H carboxyl hydroxy 2500–3000 3200–3600 Use Table 6.1 to identify the bonds responsible for the absorptions marked S and T on . S T Molecules of W, CH2=CHCN, do not show stereoisomerism. Describe stereoisomerism. Describe the two essential features of an alkene molecule that cause it to show geometrical stereoisomerism. Molecules of CH3CH(OH)CN exist as a pair of optical isomers. Draw three-dimensional diagrams in the boxes to show the optical isomers of CH3CH(OH)CN. isomer 1 isomer 2 Propanenitrile is heated with hydrogen gas and a platinum catalyst. The only product is propylamine. Construct an equation for this reaction. Propylamine can also be formed in a two-step synthesis from propan-1-ol, as shown in . CH3CH2CH2OH CH3CH2CH2Cl CH3CH2CH2NH2 step 1 SOCl 2 step 2 Name the type of reaction in step 1 in . Identify the reagent and conditions for step 2 in .