9701_s22_qp_23
A paper of Chemistry, 9701
Questions:
5
Year:
2022
Paper:
2
Variant:
3

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G belongs to a group of compounds called ethers. H H C H H C H H C H H C H H O G When G, C4H10O, is heated, thermal decomposition occurs. C4H10O→ C2H6+ CO+ CH4∆H = –7.00 kJ mol–1 The atoms in a molecule of CO are held together by a triple covalent bond. One of these bonds is a coordinate (dative covalent) bond. Draw a dot-and-cross diagram to show the arrangement of outer electrons in a CO molecule. Use ● to represent electrons from an oxygen atom. Use × to represent electrons from a carbon atom.  Calculate the bond energy of C≡O using the bond energy values in Table3.1 and the enthalpy change, ∆H, for the thermal decomposition of G. Show your working. Table 3.1 bond bond energy / kJ mol–1 C–C C–O (in G) C–H  bond energy (C≡O) = kJ mol–1  When G, C4H10O, is heated in a sealed container, an equilibrium mixture is produced. C4H10OC2H6+ CO+ CH4Complete the expression for the equilibrium constant, Kc, for this reaction. State the units of Kc. Kc =  units =  Thermal decomposition of G in the presence of I2 affects the activation energy, Ea, for the reaction. Table3.2 shows Ea for the thermal decomposition of G with and without I2. Table 3.2 reaction Ea (with I2) / kJ mol–1 Ea / kJ mol–1 C4H10O→ C2H6+ CO+ CH4143 State what effect adding I2 to the reaction mixture has on the value of Kc. Explain your answer. Fig. 3.2 shows the Boltzmann distribution of energies for molecules of G at constant temperature, T °C. Sketch, on Fig.3.2, the Boltzmann distribution of energies for molecules of G at a higher temperature, (T+100) °C. number of molecules energy Ea  The functional group in G is an oxygen atom bonded to two carbon atoms. H H C H H C H H C H H C H H O G G, H and J are structural isomers with molecular formula C4H10O. H and J are straight chain molecules. Table3.3 shows the boiling points and reactions of G, H and J when heated under reflux with excess acidified K2Cr2O7. Table 3.3 G H J boiling point / °C heat under reflux with excess acidified K2Cr2O7 remains orange orange to green orange to green Identify the type of structural isomerism shown between G and H using the information in Table3.3. Identify the type of structural isomerism shown between H and J using the information in Table3.3. Draw a possible structure for H and for J. State the systematic name for each structure. H name J name  K has molecular formula C3H6O. When K is added to 2,4-dinitrophenylhydrazine, an orange precipitate forms. When K is warmed with Tollens’ reagent, a silver mirror forms. Draw the displayed formula of K. K  
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2-methylpropene reacts with HCl at room temperature. The major organic product is 2-chloro-2-methylpropane. Complete Fig. 4.1 to show the structure of the intermediate and mechanism for this reaction. Include charges, dipoles, lone pairs of electrons and curly arrows as appropriate. C C H H H Cl Cl C H3C H3C CH3 CH3 H3C  Explain why, in this reaction, 2-chloro-2-methylpropane is produced at a higher yield than 1-chloro-2-methylpropane. Two bottles labelled Q and M each contain a straight-chain halogenoalkane with molecular formula C4H9X, where X represents Cl, Br or I. A sample from each bottle is added to separate samples of equal amounts of aqueous silvernitrate in ethanol. In each reaction, the same organic product, T, and a precipitate are made, as shown in Fig.4.2. Q T M AgNO3in ethanol AgNO3in ethanol Table4.1 describes the colour of each of the precipitates made. Table 4.1 halogenoalkane added to AgNO3in ethanol colour of precipitate Q white M yellow Identify the functional group present in T and name the type of reaction that occurs using the information in Fig.4.2 and Table4.1. functional group in T type of reaction  Construct an ionic equation to describe the formation of the yellow precipitate produced when M reacts with AgNO3in ethanol. Describe which reagent, Q or M, will produce a precipitate more quickly when each is added to AgNO3in ethanol. Explain your answer. reagent  When pure T is added to alkaline I2, a yellow precipitate and an anion, L, are made. Identify the anion L. Deduce the structure of the straight-chain halogenoalkane M.  
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