The Alkanols (Alcohols) : (General Formula: C H OH)

THE ALKANOLS (ALCOHOLS)
(General formula: CnH2n+1OH)
The alkanols are a large group of chemicals with a wide range of uses. Ethanol and the other
alkanols undergo a number of reactions based on the presence of the hydroxyl (-OH) functional
group.
Reactions with More Reactive Metals
Highly reactive metals such as sodium, lithium and calcium, react with low molecular mass
alkanols, such as methanol, ethanol and propanol. These reactions give hydrogen gas and salts of
the alkanols, called alkoxides. The equation for the reaction of ethanol with sodium metal is:
+
2𝑁𝑎(𝑠) + 2𝐶𝐻3 𝐶𝐻2 𝑂𝐻(𝑙) → 2𝐶𝐻3 𝐶𝐻2 𝑂− 𝑁𝑎(𝑠) + 𝐻2 (𝑔)
Sodium ethoxide
This reaction is similar to that of sodium and water, but is less vigorous.
Oxidation of Alkanols
Powerful oxidizing agents, such as acidified potassium dichromate (VI) or acidified potassium
manganate (VII), convert alkanols to organic acids. In these reactions, an intermediate alkanal
(or aldehyde) is formed.
𝑤𝑎𝑟𝑚 𝐾𝑀𝑛𝑂4 /𝐻 +
𝐶𝐻3 𝐶𝐻2 𝑂𝐻(𝑙 ) + [𝑂] → 𝐻2 𝑂 + 𝐶𝐻3 𝐶𝐻𝑂(𝑙)
Ethanal (intermediate)
𝑤𝑎𝑟𝑚 𝐾𝑀𝑛𝑂4 /𝐻 +
𝐶𝐻3 𝐶𝐻𝑂(𝑙 ) + [𝑂] → 𝐶𝐻3 𝐶𝑂𝑂𝐻(𝑎𝑞)
Ethanoic acid
During this reaction, the reaction mixture changes from purple to colourless. The same reactions
take place with potassium dichromate (VI), but the colour change is from orange to green.
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Dehydration of Alcohols to form Alkenes
Alkanols react with dehydrating agents, such as concentrated sulphuric acid or anhydrous
aluminium oxides, to form alkenes. The reaction is described as a dehydration. The water is lost
across two adjacent carbon atoms in the alkanol. This results in the formation of a double bond
between the two carbon atoms.
Dehydration can be achieved by:
 Heating the ethanol with excess concentrated sulphuric acid at a temperature of 170°C;
 Passing ethanol vapour over activated alumina (Al2O3) heated to 450°C.
2
Conversion of Alkanols to Esters
Another reaction of alkanols is their conversion to esters.

𝑐𝑜𝑛𝑐.𝐻2 𝑆𝑂4
𝐴𝑙𝑘𝑎𝑛𝑜𝑖𝑐 𝑎𝑐𝑖𝑑 + 𝑎𝑙𝑘𝑎𝑛𝑜𝑙 ⇔ 𝑒𝑠𝑡𝑒𝑟 + 𝑤𝑎𝑡𝑒𝑟
Combustion of Alkanols
The combustion of alkanols is a highly exothermic reaction; hence the use of alkanols, especially
methanol and ethanol, as fuel. Ethanol burns with a blue flame to yield carbon dioxide and water.
2𝐶𝐻3 𝑂𝐻(𝑙) + 3𝑂 2 (𝑔) → 2𝐶𝑂2 + 4𝐻2 𝑂(𝑔) + ℎ𝑒𝑎𝑡

𝐶2 𝐻5 𝑂𝐻(𝑙) + 3𝑂2 (𝑔) → 2𝐶𝑂2 (𝑔) + 3𝐻2 𝑂(𝑔) + ℎ𝑒𝑎𝑡
These equations represent the complete combustion of the alkanols. In an insufficient supply of
oxygen, carbon monoxide, carbon and even hydrogen may be formed. This is similar to the
combustion of hydrocarbons.
Properties and Uses of Alkanols
Like water, ethanol is a polar covalent compound. However, when compared with water, it has a
higher molar mass and higher heat of combustion, but lower melting and boiling points. The
boiling point of water is 100°C, whereas the boiling point of ethanol is 78°C. This suggests that
the intermolecular forces are weaker in ethanol than in water. Ethanol is therefore a more volatile
liquid than water.
These properties make ethanol useful as:
 a solvent;
 a fuel;
 a germicide;
 an antifreeze.
Uses of Ethanol
 Ethanol is a solvent with a wide range of uses:
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o Ethanol dissolves a wide range of substances, both polar and non-polar.
o Ethanol dissolves many compounds that do not readily dissolve in water, so it is a
complementary solvent to water.
o Many useful products are obtained by dissolving suitable substances in ethanol or
ethanol-based solvents. Among these are paints, thinners and polish, inks,
lacquers and varnishes, adhesives, deodorants and colognes, and a wide range of
pharmaceutical preparations.
o Ethanol’s volatility makes its removal as a solvent easy.
o Ethanol’s miscibility with water allows it to act as a solvent in reactions between
ionic and covalent substances.
 Large amounts of energy are released when alkanols are burnt. Alkanols, particularly
ethanol, are finding increasing use as fuels or fuel substitutes for transport and in
industry. In the Caribbean, ethanol is mixed with gasoline to produce gasohol, which is
used as an automobile fuel called E10. E10 is gasoline blended with 10% ethanol. The
ethanol contains oxygen, which raises the octane level of gasoline to prevent engine
knocking.
Production of Rum
Ethanol, the main ingredient in many alcoholic drinks such as beer, wine and rum, is obtained by
the anaerobic fermentation of grapes, sugar, molasses and other carbohydrate materials. In the
Caribbean, molasses, which is a by-product of cane sugar manufacture, is frequently used in
fermentation.
The fermentation process can be summarized as follows:
𝑠𝑢𝑔𝑎𝑟, 𝑠𝑡𝑎𝑟𝑐ℎ𝑦 𝑚𝑎𝑡𝑒𝑟𝑖𝑎𝑙𝑠 𝑜𝑟 𝑚𝑜𝑙𝑎𝑠𝑠𝑒𝑠 + 𝑒𝑛𝑧𝑦𝑚𝑒𝑠 𝑠𝑢𝑝𝑝𝑙𝑖𝑒𝑑 𝑏𝑦 𝑦𝑒𝑎𝑠𝑡

→ 𝑒𝑡ℎ𝑎𝑛𝑜𝑙 + 𝑐𝑎𝑟𝑏𝑜𝑛 𝑑𝑖𝑜𝑥𝑖𝑑𝑒
𝑒𝑛𝑧𝑦𝑚𝑒𝑠;37℃
𝐶6 𝐻12 𝑂6 → 2𝐶2 𝐻5 𝑂𝐻 + 2𝐶𝑂2
Yeasts are unicellular fungi and are the source of the enzymes that are necessary for
fermentation. Yeast cells grow rapidly and bud freely if sucrose, water, specific nitrogen sources,
vitamins and mineral salts are present.
The figure below summarizes the stages in the manufacture of rum from molasses. The final
distillation can be controlled to obtain ethanol for either industrial purposes (99.6% ethanol) or
rum (40% ethanol).
4
The distillate is processed further. Some flavours are removed during the processing and the raw
spirit is matured in oak casks before it acquires the characteristics (colour and taste) of rum.
Production of Beer
Beer is an alcoholic beverage that is brewed mainly from malted barley. Barley is a cereal grain.
Other ingredients involved in the brewing process include hops, yeast and water. Fruit, wheat
and spices are sometimes also used. During the brewing process, the yeast turns the sugars in
malt into alcohol, and the hops provide the bitter flavours in beer and the flowery aroma.
The process of beer-brewing is summarized below into seven (7) major steps:
1. Malting
2. Mashing
3. Fermentation
4. Storage
5. Filtration
6. Pasteurization
7. Packaging
The following flowchart shows the steps involved in brewing:
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The Effects of Ethanol on the Body
Ethanol can have both short-term and long-term effects on the body. Many of the immediate
effects are linked to the small size of the ethanol molecule, which allows it to pass through the
lining of the stomach, and directly into the bloodstream. This is particularly the case if ethanol is
consumed on an empty stomach. Body mass, size of liver, gender and type of alcoholic drink all
influence how rapidly the effects of drinking ethanol become evident.
Some of the short-term effects are:
 initial relaxation
 euphoria
 loss of inhibitions
 impaired co-ordination
 slowed reflexes
 slowed mental processes
 attitude changes
Ethanol is a toxic drug. A concentration of 4 parts per 1,000 in the blood can lead to a deep
anaesthetic effect or even death. When a person consistently consumes more ethanol than the
body can break down, there is a significant rise in the blood ethanol level, which leads, among
other things, to:
 impaired circulation
 accumulation of toxins
 excessive loss of fluids via urination
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 problems of digestion, hence stomach problems
 malfunction of organs such as the pancreas, liver and brain in the long term
In addition, many common drugs, e.g. aspirin and antihistamines, contain ingredients that react
unfavourably with ethanol. The simultaneous use of ethanol and such drugs can lead to
complicated health problems.

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THE ALKANOLS (ALCOHOLS)

(General formula: CnH2n+1OH)

Reactions with More Reactive Metals

Dehydration can be achieved by:

 Passing ethanol vapour over activated alumina (Al2O3) heated to 450°C.

Another reaction of alkanols is their conversion to esters.

2𝐶𝐻3 𝑂𝐻(𝑙) + 3𝑂 2 (𝑔) → 2𝐶𝑂2 + 4𝐻2 𝑂(𝑔) + ℎ𝑒𝑎𝑡

Properties and Uses of Alkanols

These properties make ethanol useful as:

 Ethanol is a solvent with a wide range of uses:

The fermentation process can be summarized as follows:

𝑠𝑢𝑔𝑎𝑟, 𝑠𝑡𝑎𝑟𝑐ℎ𝑦 𝑚𝑎𝑡𝑒𝑟𝑖𝑎𝑙𝑠 𝑜𝑟 𝑚𝑜𝑙𝑎𝑠𝑠𝑒𝑠 + 𝑒𝑛𝑧𝑦𝑚𝑒𝑠 𝑠𝑢𝑝𝑝𝑙𝑖𝑒𝑑 𝑏𝑦 𝑦𝑒𝑎𝑠𝑡

The following flowchart shows the steps involved in brewing:

Some of the short-term effects are:

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