9701_s19_qp_43
A paper of Chemistry, 9701
Questions:
9
Year:
2019
Paper:
4
Variant:
3

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Sketches of the shapes of some atomic orbitals are shown. Identify the type of orbital, s, p, or d. x y z x y z x y z shape of orbital type of orbital  Cadmium forms the two ions, Cd2 2+ and Cd2+. The electronic configuration of cadmium in these ions is shown. ● ● [Kr] 4d105s1 ● ● [Kr] 4d10 Use this information to explain why cadmium is not a transition element. Methylamine, CH3NH2, is a monodentate ligand. State what is meant by the term monodentate in this context. In the presence of aqueous methylamine, [Cd(H2O)6]2+ reacts to form a mixture of two isomeric octahedral complexes. equilibrium 1 [Cd(H2O)6]2+ + 4CH3NH2 [Cd(CH3NH2)4(H2O)2]2+ + 4H2O = –57 kJ mol–1 Complete the three-dimensional diagrams to show the isomers of [Cd(CH3NH2)4(H2O)2]2+. Use L to represent CH3NH2 in your diagrams. Cd Cd  State what is meant by the term stability constant. Complete the table by placing one tick () in each row to suggest how increasing temperature will affect Kstab and the equilibrium concentration of the cadmium complex, [[Cd(CH3NH2)4(H2O)2]2+], for equilibrium1. Explain your answer. decreases no change increases Kstab [[Cd(CH3NH2)4(H2O)2]2+] explanation  EDTA4– is a polydentate ligand. When a solution of EDTA4– is added to [Cd(H2O)6]2+ a new complex [CdEDTA]2– is formed. The values for the stability constants for two Cd2+ complexes are shown. Kstab [Cd(CH3NH2)4(H2O)2]2+ 4.0 × 106 [CdEDTA]2– 4.0 × 1016 A solution containing equal numbers of moles of CH3NH2 and EDTA is added to [Cd(H2O)6]2+. Predict which complex is formed in the larger amount. Explain your answer. Methylamine is a Brønsted-Lowry base. Write an equation showing how methylamine dissolves in water to give an alkaline solution. Methylamine is a useful reagent in organic chemistry. Write an equation for the reaction of ethanoyl chloride with methylamine. Methylamine also reacts with propanone to form compound P as shown. H3C H3C C O H2N CH3 CH3 + H2O + H3C H3C C N P Deduce the type of reaction shown here. 
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Benzene can be converted into cyclohexane. For this reaction name the type of reaction and identify the reagent and conditions needed. type of reaction reagent and conditions  State the bond angles in benzene and cyclohexane. bond angle in benzene bond angle in cyclohexane Explain your answers.  When benzene reacts with SO3, benzenesulfonic acid is produced. SO3H benzenesulfonic acid + SO3 The mechanism of this reaction is similar to that of the nitration of benzene. Concentrated H2SO4 is used in an initial step to generate the SO3H+ electrophile as shown. SO3 + H2SO4 SO3H+ + HSO4 – Draw a mechanism for the reaction of benzene with SO3H+ ions. Include all necessary curly arrows and charges. SO3H benzenesulfonic acid SO3H+  Write an equation to show how the H2SO4 catalyst is reformed. 3-dodecylbenzenesulfonic acid can be prepared from benzenesulfonic acid. 3-dodecylbenzenesulfonic acid SO3H SO3H C12H25 benzenesulfonic acid Suggest the reagents and conditions and name the mechanism for this reaction. reagents and conditions mechanism  When concentrated sulfuricacid is added to water, dissociation takes place in two stages. stage 1 H2SO4 H+ + HSO4 – stage 2 HSO4 – H+ + SO4 2– Ka2 = 1.0 × 10–2 mol dm–3 Ka2 is the acid dissociation constant for stage 2. Write the expression for the acid dissociation constant Ka2. Ka2 =  H2SO4 is considered a strong acid whereas HSO4 – is considered a weak acid. Suggest how the magnitude of the acid dissociation constant for stage1 compares to Ka2. Benzoic acid, C6H5CO2H, is a weak acid. A solution of 0.0250 mol dm–3 benzoic acid has a pH of 2.90. Calculate the Ka of benzoic acid.  Ka = mol dm–3  
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Organochlorine compounds can undergo hydrolysis. R–Cl + H2O R–OH + HCl State and explain the relative rates of hydrolysis of the following compounds. CH3CH2Cl CH3COCl C6H5Cl Epibatidine is a naturally occurring organochlorine compound. Cl N epibatidine N H Epibatidine is a weak base. State what is meant by the term weak base. A molecule of epibatidine contains two nitrogen atoms, both of which can act as a base. Epibatidine reacts with HCl . Complete the structure to suggest the product formed in this reaction. Cl N N H  Polyamides, such as nylon-6, can be prepared from a monomer that contains both an amine and an acyl chloride functional group. nylon-6 monomer H2N (CH2)5 C O Cl When the nylon-6 monomer is hydrolysed, bonds are broken and formed. By considering the two steps in the mechanism of the reaction, complete the table by placing one tick () in each row to indicate the types of bonds broken and formed during the mechanism. σ bonds only π bonds only both σ and π bonds bonds broken bonds formed  Draw two repeat units of nylon-6. The amide bond should be shown fully displayed.  An addition polymer made from two different alkene monomers is called a co-polymer. A section of a polyalkene co-polymer is shown. C CH3 Cl C H H H C C2H5 C H C CH3 CH3 Cl C H H Draw the structure of the two alkene monomers which produce this co-polymer.  Explain why polyamides normally biodegrade more readily than polyalkenes. The alkene phenylethene can be prepared from benzene in three steps. step 1 step 3 step 2 O H phenylethene Deduce the identity of compound H and draw its structure in the box. Suggest reagents and conditions for each of the steps 1–3. step 1 step 2 step 3