(a) The letters R,S,T represent an alkene, an alkene and a terminal alkyne respectively. Which of R, S and T typically undergo(es) the following reactions? ...
(a) The letters R,S,T represent an alkene, an alkene and a terminal alkyne respectively. Which of R, S and T typically undergo(es) the following reactions?
(i) Addition reaction;
(ii) Combustion;
(iii) Substitution reaction.
(b)(i) Name the process by which an alkanol can be converted to an alkene.
(ii) Write the name and structural formula of the third member cf the alkanol series.
(iii) State what would be obtained if a primary alkanol reacted with excess acidified KMnO\(_4\) solution.
(c)(i) Give one chemical test for alkanoic acids.
(ii) Write an equation to show how methanoic acid reacts with ethanol in the presence of mineral acids.
(iii) What is the role of mineral acid in the reaction in (c) ii?
(d) In an experiment, cassava was pressure-cooked to release starch granules, followed by treatment with malt for about 2 hours at 55°C. Yeast was then added and the mixture was left for 2 days at 27°C. An organic product J and a gas H were obtained.
(i) Identify H
(ii) State the class of carbohydrates to which starch belongs and explain what happened to the starch during treatment with malt.
(iii) Draw a labelled diagram of a suitable set-up for obtaining a sample of J from the reaction mixture.
(a)
Taking R as an alkane, S as an alkene and T as a terminal alkyne:
Addition reaction: S and T.
Combustion: R, S and T.
Substitution reaction: R and T.
(b)
The process is dehydration of the alkanol.
The third member is propan-1-ol. Structural formula: CH3CH2CH2OH.
A primary alkanol is oxidised to the corresponding alkanoic acid by excess acidified potassium manganate(VII) solution. For example: \[\mathrm{CH_3CH_2OH + 2[O] \rightarrow CH_3COOH + H_2O}\]
(c)
Add aqueous sodium hydrogencarbonate or sodium carbonate to the acid. Brisk effervescence of carbon dioxide is produced. \[\mathrm{RCOOH + NaHCO_3 \rightarrow RCOONa + CO_2 + H_2O}\]
The mineral acid acts as a catalyst in the esterification reaction.
(d)
H is carbon dioxide, CO2.
Starch is a polysaccharide. The diastase (amylase) enzyme in malt hydrolyses starch to maltose, a reducing sugar. \[\mathrm{(C_6H_{10}O_5)_n + \tfrac{n}{2}H_2O \xrightarrow[55^{\circ}C]{diastase} \tfrac{n}{2}C_{12}H_{22}O_{11}}}\]
Yeast subsequently ferments the sugar to ethanol, J, and carbon dioxide:
Taking R as an alkane, S as an alkene and T as a terminal alkyne:
Addition reaction: S and T.
Combustion: R, S and T.
Substitution reaction: R and T.
(b)
The process is dehydration of the alkanol.
The third member is propan-1-ol. Structural formula: CH3CH2CH2OH.
A primary alkanol is oxidised to the corresponding alkanoic acid by excess acidified potassium manganate(VII) solution. For example: \[\mathrm{CH_3CH_2OH + 2[O] \rightarrow CH_3COOH + H_2O}\]
(c)
Add aqueous sodium hydrogencarbonate or sodium carbonate to the acid. Brisk effervescence of carbon dioxide is produced. \[\mathrm{RCOOH + NaHCO_3 \rightarrow RCOONa + CO_2 + H_2O}\]
The mineral acid acts as a catalyst in the esterification reaction.
(d)
H is carbon dioxide, CO2.
Starch is a polysaccharide. The diastase (amylase) enzyme in malt hydrolyses starch to maltose, a reducing sugar. \[\mathrm{(C_6H_{10}O_5)_n + \tfrac{n}{2}H_2O \xrightarrow[55^{\circ}C]{diastase} \tfrac{n}{2}C_{12}H_{22}O_{11}}}\]
Yeast subsequently ferments the sugar to ethanol, J, and carbon dioxide: