Edexcel Jan 2013 Paper 4 Q17

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17 Ethanoic acid and ethanol react together to form the ester ethyl ethanoate, CH3COOC2H5, and water. CH3COOH(l) + CH3CH2OH(l) U CH3COOCH2CH3(l) + H2O(l) (a) (i) Give the expression for Kc. (ii) An equilibrium was reached when the amounts of substances shown in the table below were used. Complete the table to show the amounts of each substance present at equilibrium. Component Initial amount / mol Equilibrium amount / mol CH3COOH(l) CH3CH2OH(l) CH3COOCH2CH3(l) 0.40 0.20 0.30 0.00 (iii) Explain why Kc for this reaction has no units. (1) (2) H2O(l) 0.15 (1)(iv) Calculate the numerical value of Kc. (1) *P41214A01728* 17 Turn over<br />
 (b) The esterification reaction above was carried out in the presence of hydrochloric acid as the catalyst. State the effect on the equilibrium position and the rate of attainment of equilibrium if the concentration of the acid catalyst were to be increased. (2)(c) (i) Identify which bonds are broken and which bonds are made in the esterification reaction. Bonds broken: Bonds made: (ii) Explain why H for this reaction is not exactly zero. (A calculation is not required.) (2) (1)(d) (i) State the relationship between Stotal and the equilibrium constant, K, of a reaction. (1) 18 *P41214A01828*<br />
 *(ii) Use entropy considerations and your answer to (d)(i) to predict any effect of an increase in temperature on the value of the equilibrium constant of a reaction for which H is zero. Assume that Ssystem does not change with temperature. (3)(e) An alternative method for preparing ethyl ethanoate is to react ethanoyl chloride with ethanol. (i) Give the equation for the reaction. (ii) Draw the skeletal formula of ethyl ethanoate. (iii) Ethanoyl chloride also reacts with concentrated ammonia. Draw the displayed formula of the organic product of this reaction. (1) (1) (1) *P41214A01928* 19 Turn over<br />
 (f) (i) Complete the equation below for the alkaline hydrolysis of ethyl ethanoate using sodium hydroxide. State symbols are not required. CH3COOCH2CH3 + NaOH o (ii) Explain why the reaction in (f)(i) gives a better yield of the alcohol compared with acid hydrolysis of the ethyl ethanoate. (1) (1)(Total for Question 17 = 19 marks) 20 *P41214A02028*<br />
 BLANK PAGE *P41214A02128* 21 Turn over<br />

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