(a) Give the products of the following reactions: (i) hydrolysis of simple proteins. (ii) alkaline hydrolysis of fats and oils. (b) A combustion tube was pa...

Assessment: WAEC SSCE - Chemistry - 1992 (Essay) Subject: Chemistry

Question 1 Report

(a) Give the products of the following reactions:

(i) hydrolysis of simple proteins.

(ii) alkaline hydrolysis of fats and oils.

 

(b) A combustion tube was packed with small pieces of broken clay pot and the tube maintained at a temperature of 750K. When the vapour of decane was passed into the tube, the main products included a gaseous hydrocarbon X.

(i) Name the process involved in the reaction. Give its industrial application.

(ii) State the function of the pieces of broken pot in the experiment.

(iii) Give one chemical test to distinguish between X and methane.

(iv) Draw a labelled diagram for the laboratory preparation of X.

 

(c)(i) State what would be observed if a piece of sodium was added to 10cm\(^3\) of propanol in a beaker. Write an equation for the reaction.

(ii) Give the main product formed when excess acidified potassium heptaoxodichromate (VI) reacts with each of the following: propan-1- ol: propan - 2 -of; State the type of process involved in the reactions.

Answer Details

(a)

  1. Hydrolysis of simple proteins produces amino acids.
  2. Alkaline hydrolysis of fats and oils produces soap (the sodium or potassium salts of fatty acids) and glycerol.

(b)

  1. The process is cracking. It is used industrially to convert large, less useful and less demanded hydrocarbon fractions into smaller, more useful fractions such as petrol and alkenes.
  2. The broken pieces of clay pot prevent local overheating and provide a medium for more uniform heating in the combustion tube.
  3. Pass each gas through bromine water, or expose it to bromine vapour. Hydrocarbon X decolourises the reddish-brown bromine water because it is an unsaturated hydrocarbon (an alkene), whereas methane produces no change.
  4. Laboratory preparation of ethene
    Ethene is prepared by dehydrating ethanol with concentrated tetraoxosulphate(VI) acid at about 170°C. The ethene formed is collected over water.
figure
Laboratory preparation and collection of ethene by dehydration of ethanol.

Equation:

\[\mathrm{CH_3CH_2OH\ \xrightarrow[170^\circ C]{conc.\ H_2SO_4}\ CH_2{=}CH_2 + H_2O}\]

(c)

  1. There is effervescence as sodium gradually dissolves. Hydrogen gas is evolved and it gives a pop sound with a lighted splint. Sodium propoxide is formed.

    \[\mathrm{2CH_3CH_2CH_2OH + 2Na \rightarrow 2CH_3CH_2CH_2ONa + H_2}\]
  2. With excess acidified potassium heptaoxodichromate(VI):
    • Propan-1-ol is oxidised to propanoic acid, \(\mathrm{CH_3CH_2COOH}\).
    • Propan-2-ol is oxidised to propanone, \(\mathrm{CH_3COCH_3}\).
    The process is oxidation.

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