9701_w22_qp_21
A paper of Chemistry, 9701
Questions:
5
Year:
2022
Paper:
2
Variant:
1

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Some of the common chlorides of Period3 elements are shown in the list. NaCl MgCl 2 Al Cl 3 SiCl 4 PCl 5 From this list, identify: all the chlorides that have giant ionic structures in the solid state all the chlorides that react vigorously with water to form strongly acidic solutions the chloride that dissolves in water to form a neutral solution the chloride formed from the element with the highest melting point. NaCl is one product of the reaction of chlorine gas and cold aqueous sodium hydroxide. Identify the other products. PCl 5 reacts with alcohols to form chloroalkanes. Identify this type of reaction. Draw the structure of the organic product formed in the reaction of an excess of PCl 5 with butane-1,3-diol.  Sulfur, S8, reacts with chlorine to form several different chlorides. The most common are S2Cl 2 and SCl 2. SCl 2 forms when sulfur reacts with an excess of chlorine. reaction1 S8+ 4Cl 2→ 4S2Cl 2∆Hr = –58.2 kJ mol–1 reaction2 S2Cl 2+ Cl 22SCl 2∆Hr = –40.6 kJ mol–1 SCl 2 is a cherry-red liquid that reacts vigorously with water to form an acidic solution. Use this information to deduce the bonding and structure shown by SCl 2. Explain your answer. Calculate the enthalpy change of formation, ∆Hf, of SCl 2. You may find it useful to use Hess’s Law to construct an energy cycle.  enthalpy change of formation of SCl 2, ∆Hf = kJ mol–1  State the effect of a decrease in pressure on the position of equilibrium in reaction2. Explain your answer. Fig.3.1 shows the two structural isomers of S2Cl 2. isomer I isomer II Cl Cl S S Cl Cl S S Define the term structural isomer. Suggest a value for the Cl –S–S bond angle in isomerI. Explain your answer. bond angle = ° explanation  Draw a dot-and-cross diagram to show the bonding in isomerII. Show outer shell electrons only.  
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Lactones are cyclic esters. Under suitable conditions, lactones form from molecules that have both an alcohol and a carboxylic acid functional group. Equation1 shows an example of the formation of a lactone. equation 1 + H2O OH OH O O a lactone O Fig.5.1 shows the synthesis of lactoneP from compoundM. O OH HO M N P hot concentrated acidified KMnO4reaction 1 NaBH4 5-hydroxyhexanoic acid reaction 2 reaction 3 M reacts with hot concentrated acidified KMnO4to form N, C6H10O3, in reaction1. Draw the structure of N.  N is reduced by NaBH4 to form 5-hydroxyhexanoic acid in reaction2. Construct an equation for reaction2 using molecular formulae. In the equation, use [H] to represent one atom of hydrogen from the reducing agent. Reaction2 is a nucleophilic addition. Suggest why reaction2 creates a mixture of two organic compounds. Draw lactoneP, the product of reaction3.  A student monitors the progress of reaction2 using infrared spectroscopy. Use Table5.1 to suggest why it is difficult to distinguish between N and 5‑hydroxyhexanoic acid using infrared spectroscopy. Table 5.1 bond functional group 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 2850–3100 N–H amine, amide 3300–3500 O–H carboxyl hydroxy 2500–3000 3200–3650 Unknown lactoneQ is analysed using mass spectrometry. Table5.2 shows information from the mass spectrum. Table 5.2 peak m/e abundance M+ 95.5 M+1 3.15 Use these data to deduce the structure of Q. Show your working. Q