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Lesson 4. IMPORTANT PROPERTIES OF MONO, DI AND TRIHYDRIC ALCOHOLS (GLYCOL AND GLYCEROL)
Module 2. Alcohols, aldehydes and ketones
Lesson 4
IMPORTANT PROPERTIES OF MONO, DI AND TRIHYDRIC ALCOHOLS (GLYCOL AND GLYCEROL)
- Organic hydroxyl compounds of the general formula R-OH, where ‘R’ is an alkyl or substituted alkyl group
- For example (Fig. 4.1)
- Contain hydroxyl (-OH) group as the functional group - determines characteristics and properties of this family.
Classified on different basis
- Based on number of hydroxyl groups
- According to number of hydroxyl groups content
- As mono-, di-, tri- and polyhydroxy (Fig. 4.2)
- Based on kind of carbon atom/ degree of carbon atom to which –OH is attached.
- According to the kind of carbon atom that bears hydroxyl group
- A carbon atom may be classified as primary, secondary and tertiary
- According to number of carbon atoms attached it (Fig. 4.3)
- Aliphatic alcohols and Aromatic alcohols
- Alcohols of different classes differ in rate and/or mechanism of reaction
- Substitution may also affect the reactivity and physical constants.
- Alcohols are considerably different from hydrocarbons due to presence of polar
–OH group – polar compounds
- Form intermolecular hydrogen bonds – as shown already
- Their boiling points are much higher
- Lower members (methanol, ethanol and propanol-1) are miscible with water
- Ethylene glycol is used as an antifreeze in automobiles.
- Determined by its functional group- hydroxyl group → -OH
- Reactions of an alcohol can involve the breaking of either of two bonds =
1. C-OH bond - leads to removal of -OH group or
2. O-H bond - leads to removal of -H
2. O-H bond - leads to removal of -H
- In either kind substitution or elimination takes place.
- The substitution replaces –OH or –H
- The elimination forms double bond
- There are two principal ways to get the simple alcohols = by hydration of alkenes and by fermentation of carbohydrates
- Alkene - obtained by cracking of petroleum
- converted into alcohol by addition of water (Fig. 4.4)
4.2.3.2 Fermentation of carbohydrates
- Fermentation of sugars by yeast is used for manufacture of ethyl alcohol
Fig. 4.5 Fermentation reactions
- The sugars come from a variety of sources - mostly from molasses from sugar cane or starch from grains (maize, peas, potatoes etc).
Widely used
- As a solvent for lacquers, varnishes, perfumes and flavoring
- As a medium for chemical reactions and in recrystallizations
- As an important raw material for synthesis of aliphatic compounds – alkenes, alkyl halides, ethers, aldehydes, ketones, acids, esters etc
- To be considered as ethyl alcohol
- Generally ethyl alcohol used is a mixture of 95% alcohol and 5% water
- After production alcohol is purified and concentrated by fractional distillation
- In distillation first material to distill is the one which has the highest volatility i.e. lowest boiling point
- In a mixture of ethyl alcohol and water the lowest boiling component is not water (boiling point 100°C) or ethyl alcohol (boiling point 72.30°C) but a mixture of alcohol and water (95:5) since its boiling point is 78.15°C therefore ethyl alcohol is concentrated upto 95%
- A liquid mixture that has the peculiar property of giving a vapour of the same composition is called azeotrope or constant-boiling mixture
- 100% ethyl alcohol is called absolute alcohol
- Obtained by taking advantage of the another azeotrope
- When a mixture containing 150 g of 95% alcohol and 74 g benzene is distilled – a ternary azeotrope consisting of 7.5% water, 18.5% alcohol and 74% benzene distilled off first due to its lower boiling point (64.90°C), leaving pure (anhydrous) alcohol behind
- Traces of water from the absolute alcohol can be removed by treatment with metallic magnesium
- Water is converted into Mg(OH)2 from which alcohol is distilled.
Last modified: Wednesday, 26 September 2012, 4:03 AM