(a)(i) What type of reaction is involved in each of the conversion processes indicated as I to V below?

(ii) Name one isomer of glucose
(iii) Explain why palmwine becomes sour on prolonged exposure to air.
(b)(i) List the reagents and the reaction condition necessary for ethanoic acid to form an alkanoate.
(ii) Give two uses of alkanoates
(c)(i) What is the lUPAC name of the following compound?

(ii) Outline one chemical test to distinguish between methane and the compound in (c)(i) above.
(iii) Write an equation for the combustion of ethene in excess oxygen.
(a)(i) Type of reaction in each conversion (I to V)
| Step | Type of reaction |
|---|
| I | Hydrolysis |
| II | Fermentation (decomposition) |
| III | Dehydration |
| IV | Polymerization |
| V | Oxidation |
(a)(ii) One isomer of glucose: fructose (galactose is also acceptable), each of formula C6H12O6.
(a)(iii) Why palm wine becomes sour on prolonged exposure to air. Palm wine contains ethanol. On exposure to air, bacterial/atmospheric oxidation converts the ethanol to ethanoic (acetic) acid, and it is this acid that gives the drink its sour taste:
\[ CH_3CH_2OH + O_2 \rightarrow CH_3COOH + H_2O \]
(b)(i) Reagents and conditions for ethanoic acid to form an alkanoate
- An alkanol (e.g. ethanol).
- Concentrated H2SO4 (or dry HCl) as catalyst/dehydrating agent.
- Heat, about \(40^\circ\text{C}\) to \(110^\circ\text{C}\), or refluxing.
\[ CH_3COOH + C_2H_5OH \underset{\Delta}{\overset{conc.\,H_2SO_4}{\rightleftharpoons}} CH_3COOC_2H_5 + H_2O \]
(b)(ii) Two uses of alkanoates (esters)
- In the manufacture of perfumes, flavours and cosmetics.
- As solvents in the paint, pharmaceutical and food industries; also for making polyester fibres.
(c)(i) IUPAC name of the compound: but-2-yne, \( CH_3-C{\equiv}C-CH_3 \).
(c)(ii) Chemical test to distinguish methane from but-2-yne. Pass each gas in turn into bromine water (or acidified KMnO4). But-2-yne, being unsaturated, rapidly decolourizes the reagent; methane, being saturated, gives no visible reaction and the colour remains.
(c)(iii) Combustion of ethene in excess oxygen
\[ C_2H_{4(g)} + 3O_{2(g)} \rightarrow 2CO_{2(g)} + 2H_2O_{(g)} \]
(a)(i) Type of reaction in each conversion (I to V)
| Step | Type of reaction |
|---|
| I | Hydrolysis |
| II | Fermentation (decomposition) |
| III | Dehydration |
| IV | Polymerization |
| V | Oxidation |
(a)(ii) One isomer of glucose: fructose (galactose is also acceptable), each of formula C6H12O6.
(a)(iii) Why palm wine becomes sour on prolonged exposure to air. Palm wine contains ethanol. On exposure to air, bacterial/atmospheric oxidation converts the ethanol to ethanoic (acetic) acid, and it is this acid that gives the drink its sour taste:
\[ CH_3CH_2OH + O_2 \rightarrow CH_3COOH + H_2O \]
(b)(i) Reagents and conditions for ethanoic acid to form an alkanoate
- An alkanol (e.g. ethanol).
- Concentrated H2SO4 (or dry HCl) as catalyst/dehydrating agent.
- Heat, about \(40^\circ\text{C}\) to \(110^\circ\text{C}\), or refluxing.
\[ CH_3COOH + C_2H_5OH \underset{\Delta}{\overset{conc.\,H_2SO_4}{\rightleftharpoons}} CH_3COOC_2H_5 + H_2O \]
(b)(ii) Two uses of alkanoates (esters)
- In the manufacture of perfumes, flavours and cosmetics.
- As solvents in the paint, pharmaceutical and food industries; also for making polyester fibres.
(c)(i) IUPAC name of the compound: but-2-yne, \( CH_3-C{\equiv}C-CH_3 \).
(c)(ii) Chemical test to distinguish methane from but-2-yne. Pass each gas in turn into bromine water (or acidified KMnO4). But-2-yne, being unsaturated, rapidly decolourizes the reagent; methane, being saturated, gives no visible reaction and the colour remains.
(c)(iii) Combustion of ethene in excess oxygen
\[ C_2H_{4(g)} + 3O_{2(g)} \rightarrow 2CO_{2(g)} + 2H_2O_{(g)} \]