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CLAIRE N. MONGCAL, LPT
ALCOHOLS
(ORGANIC CHEMISTRY)
TABLE OF CONTENTS
PROPERTIES
01
STRUCTURE
02
REACTIONS
04
03
NOMECLATURE
05
06
USES/
APPLICATIONS
ACTIVITY
OF
ALCOHOLS
01
PROPERTIES
WHAT IS ALCOHOL?
Alcohols are the organic compounds in which a hydrogen
atom or an aliphatic carbon is replaced with the hydroxyl
group. Thus an alcohol molecule consists of two parts;
one containing the alkyl group and the other containing
the hydroxyl group. They have a sweet odor. They exhibit
a unique set of physical and chemical properties. These
physical and chemical properties of alcohols are mainly
due to the presence of hydroxyl group. The alcohol
structure depends on various factors.
Properties of alcohol can be explained by the
following points –
 Alcohols are colorless.
 They generally give a sweet smell except for glycerol and a few
lower alcohols.
 They are flammable and produce a blue flame.
 They don’t produce any smoke while burning.
 They are generally liquid at room temperature. Although glycerol is a
viscous liquid.
 Boiling Point of Alcohol - They generally have higher boiling points if
we compare them with other hydrocarbons. For example, ethanol
shows a boiling point of 78.29℃ while hexane shows a boiling point
of 69℃. This is because of the presence of intermolecular hydrogen
bonding between hydroxyl groups of alcohols. The boiling point of
alcohol increases with an increasing number of carbon atoms in
organic alcoholic compounds.
 Alcohols work as suitable solvents for many organic compounds as
organic compounds are insoluble in water.
 Alcohols are acidic in nature. They react with metals such as sodium,
potassium etc. It is due to the polarity of the bond between a hydrogen
atom and the oxygen atom of the hydroxyl group. Primary alcohols are
more acidic than secondary and tertiary alcohols.
 Due to the polar -OH bond in alcohols, they are more soluble in water
than other simple hydrocarbons. For example, methanol and ethanol
are miscible in water.
OF
ALCOHOLS
02
STRUCTURE
Alcohol structure is mainly attributed
to the presence of the hydroxyl group.
In alcohols, the carbon atom of the
main chain is bonded to the oxygen
atom of the hydroxyl group by a sigma
(σ) bond. This sigma bond is formed
due to the overlap of an sp3
hybridized
orbital of carbon with an sp3
hybridized
orbital of oxygen. Due to the repulsion
between the unshared electron pairs
of oxygen, the bond angle of C-O-H
bonds in alcohols is slightly less than
the tetrahedral angle (109°-28′).
Alcohols are considered to be as the derivatives of water
where one among the hydrogen atoms are replaced by
alkyl group, which is typically represented by the letter R
in an organic structure. Alcohol also comes in different
structures and forms.
Alcohols are known to be one among most of the
commonly occurring organic compounds. These are
utilized in the form of sweeteners, preparation of
perfumes, and sometimes in the process of synthesizing
other compounds, wherein some others are abundantly
manufactured in organic chemicals coming in various
industries.
Alcohols are differentiated based upon the presence of the
hydroxyl group attached. The location of this hydroxyl
group as well will change the physical and chemical
properties of any alcohol.
Classification of alcohol based on the number of OH present.
1. Monohydric alcohols- contains one OH group. (CnH2nOH )
Example: CH3CH2OH
2. Dihydric alcohols- contains 2 OH group. (CnH2n(OH)2)
Example: CH2-OH
CH2-OH
Main Types of Alcohols
ETHANO
L
ETHYLENE GLYCOL
3.Trihydric alcohols- contains 3 OH group. ( (CH2)n(OH)3 )
Example:
4. Polyhydric alcohols- contains many OH group.
Example:
GLYCEROL
GLUCOSE
There are three types of alcohol based on the number of
carbons (Monohydric). Alcohols are classified as primary,
secondary or tertiary alcohols.
The classification is done in accordance with the carbon
atom of an alkyl group is attached to the hydroxyl group.
Most of the alcohols are known to be colorless liquids or
even are said to behave as solid at room temperatures.
Alcohols with less molecular weight are said to be highly
soluble in water; and with their increase in molecular
weight, they tend to become less soluble and their vapor
pressures, boiling points, densities, and the viscosities to
increase.
Let us study in brief about the types of monohydric alcohols.
1. Primary Alcohols
Primary alcohols are those alcohols where the carbon atom of the
hydroxyl group (OH) is attached to only one single alkyl group.
Some examples of these primary alcohols include Methanol
(propanol), ethanol, etc. The complexity of this alkyl chain is
unrelated to the classification of any alcohol considered as primary.
The existence of only one linkage among –OH group and an alkyl
group and the thing that qualifies any alcohol as a primary. (RCH2OH)
2. Secondary Alcohols
Secondary alcohols are those where the carbon atom of the
hydroxyl group is attached to two alkyl groups on either side. The
two alkyl groups present may be either structurally identical or even
different. Some examples of secondary alcohols are given below.
(R2CHOH)
3. Tertiary Alcohols
Tertiary alcohols are those which feature a hydroxyl group attached
to the carbon atom which is connected to 3- alkyl groups. The
physical properties of these alcohols mainly depend on their
structure. The presence of this -OH group allows the alcohols in the
formation of hydrogen bonds with their neighboring atoms. The
bonds formed are weak, and this bond makes the boiling points of
alcohols higher than its alkanes. (R3CHOH ) Examples of tertiary
alcohols include-
OF
ALCOHOLS
03
NOMECLATURE
As with other types of organic compounds,
alcohols are named by both formal and common
systems. The most generally applicable system
is that adopted at a meeting of the
International Union of Pure and Applied Chemist
ry
(IUPAC) in Paris in 1957. Using the IUPAC
system, the name for an alcohol uses the -ol
suffix with the name of the parent alkane,
together with a number to give the location of
the hydroxyl group. The rules are summarized in
a three-step procedure:
1.The longest continuous chain (LCC) of carbon atoms containing
the OH group is taken as the parent compound -- an alkane with the
same number of carbon atoms. The chain is numbered from the
end nearest the OH group.
2.The number that indicates the position of the OH group is
prefixed to the name of the parent hydrocarbon, and the -e ending
of the parent alkane is replaced by the suffix -ol. (In cyclic alcohols,
the carbon atom bearing the OH group is designated C1, but the 1
is not used in the name.) Substituents are named and numbered as
in alkanes.
3.If more than one OH group appears in the same molecule
(polyhydroxy alcohols), suffixes such as -diol and -triol are used. In
these cases, the -e ending of the parent alkane is retained.
13.-ALCOHOLS and its functional gro.pptx
13.-ALCOHOLS and its functional gro.pptx
13.-ALCOHOLS and its functional gro.pptx
13.-ALCOHOLS and its functional gro.pptx
OF
ALCOHOLS
04
REACTIONS
 Oxidation Reaction of Alcohol – Alcohols produce aldehydes and
ketones on oxidation. The reaction is given below –
C₂H₅OH + 2O CH₃COOH + H₂O
Ethanol Ethanoic acid
 Combustion of Alcohol – On heating ethanol gives carbon dioxide
and water and burns with a blue flame. The reaction is given below –
C₂H₅OH + 3O₂ 2CO₂ + 3H₂O
→
→
 Dehydration of Alcohol – Alcohol can be dehydrated in an acidic
medium. The removal of water molecules from a compound is called
dehydration. Upon dehydration of alcohol alkenes are produced. The
reaction is given below –
C2H5OH (conc. H₂SO₄,▵)→C₂H₄ + H₂O
 The reaction of Alcohol With Metal – Due to its acidic nature alcohol
reacts with metal and forms alkoxide. For example, when ethanol
reacts with sodium forms sodium ethoxide and hydrogen gas. The
reaction is given below –
2C₂H₅OH + 2Na →2C₂H₅ONa + H₂
 Formation of Halides From Alcohols – Alcohol reacts with HCl and
forms alkyl halides by removal of hydroxyl groups. The reaction is
given below
ROH + HCl (Zn) → R-Cl + H₂
 Esterification – Alcohol reacts with a carboxylic acid in presence of a
catalyst and forms ester. It is called Fischer esterification. The
reaction is given below –
C₂H₅OH + C₂H5COOH →C₄H₈O₂ + H₂O
13.-ALCOHOLS and its functional gro.pptx
OF
ALCOHOLS
05
USES/
APPLICATION
 Alcohols are consumed as beverages where the alcohols
specifically consist of 30–40 per cent of ethanol by volume.
 These are used as an anti-freezing agent with a mixture of a
solution containing ethylene glycol dissolved in water.
 Alcohol ethanol is used as an antiseptic agent.
 Some alcohols are used as fuels in internal combustion engines
like the methanol.
 In the field of medicine, a few of them are used
as preservatives for the specimens in laboratories.
Uses of Alcohols
06
ACTIVITY
NAME THE FOLLOWING…
1.What is alcohol?
2.What are the different types of alcohols?
3.Differentiate Monohydric, Dihydric,
Trihydric and Polyhydric.
4.Differentiate Primary, Secondary and
Tertiary alcohols.
5.What are the uses of alcohol?
THANK
YOU!

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13.-ALCOHOLS and its functional gro.pptx

  • 1. CLAIRE N. MONGCAL, LPT ALCOHOLS (ORGANIC CHEMISTRY)
  • 4. WHAT IS ALCOHOL? Alcohols are the organic compounds in which a hydrogen atom or an aliphatic carbon is replaced with the hydroxyl group. Thus an alcohol molecule consists of two parts; one containing the alkyl group and the other containing the hydroxyl group. They have a sweet odor. They exhibit a unique set of physical and chemical properties. These physical and chemical properties of alcohols are mainly due to the presence of hydroxyl group. The alcohol structure depends on various factors.
  • 5. Properties of alcohol can be explained by the following points –  Alcohols are colorless.  They generally give a sweet smell except for glycerol and a few lower alcohols.  They are flammable and produce a blue flame.  They don’t produce any smoke while burning.  They are generally liquid at room temperature. Although glycerol is a viscous liquid.
  • 6.  Boiling Point of Alcohol - They generally have higher boiling points if we compare them with other hydrocarbons. For example, ethanol shows a boiling point of 78.29℃ while hexane shows a boiling point of 69℃. This is because of the presence of intermolecular hydrogen bonding between hydroxyl groups of alcohols. The boiling point of alcohol increases with an increasing number of carbon atoms in organic alcoholic compounds.  Alcohols work as suitable solvents for many organic compounds as organic compounds are insoluble in water.
  • 7.  Alcohols are acidic in nature. They react with metals such as sodium, potassium etc. It is due to the polarity of the bond between a hydrogen atom and the oxygen atom of the hydroxyl group. Primary alcohols are more acidic than secondary and tertiary alcohols.  Due to the polar -OH bond in alcohols, they are more soluble in water than other simple hydrocarbons. For example, methanol and ethanol are miscible in water.
  • 9. Alcohol structure is mainly attributed to the presence of the hydroxyl group. In alcohols, the carbon atom of the main chain is bonded to the oxygen atom of the hydroxyl group by a sigma (σ) bond. This sigma bond is formed due to the overlap of an sp3 hybridized orbital of carbon with an sp3 hybridized orbital of oxygen. Due to the repulsion between the unshared electron pairs of oxygen, the bond angle of C-O-H bonds in alcohols is slightly less than the tetrahedral angle (109°-28′).
  • 10. Alcohols are considered to be as the derivatives of water where one among the hydrogen atoms are replaced by alkyl group, which is typically represented by the letter R in an organic structure. Alcohol also comes in different structures and forms. Alcohols are known to be one among most of the commonly occurring organic compounds. These are utilized in the form of sweeteners, preparation of perfumes, and sometimes in the process of synthesizing other compounds, wherein some others are abundantly manufactured in organic chemicals coming in various industries.
  • 11. Alcohols are differentiated based upon the presence of the hydroxyl group attached. The location of this hydroxyl group as well will change the physical and chemical properties of any alcohol. Classification of alcohol based on the number of OH present. 1. Monohydric alcohols- contains one OH group. (CnH2nOH ) Example: CH3CH2OH 2. Dihydric alcohols- contains 2 OH group. (CnH2n(OH)2) Example: CH2-OH CH2-OH Main Types of Alcohols ETHANO L ETHYLENE GLYCOL
  • 12. 3.Trihydric alcohols- contains 3 OH group. ( (CH2)n(OH)3 ) Example: 4. Polyhydric alcohols- contains many OH group. Example: GLYCEROL GLUCOSE
  • 13. There are three types of alcohol based on the number of carbons (Monohydric). Alcohols are classified as primary, secondary or tertiary alcohols.
  • 14. The classification is done in accordance with the carbon atom of an alkyl group is attached to the hydroxyl group. Most of the alcohols are known to be colorless liquids or even are said to behave as solid at room temperatures. Alcohols with less molecular weight are said to be highly soluble in water; and with their increase in molecular weight, they tend to become less soluble and their vapor pressures, boiling points, densities, and the viscosities to increase.
  • 15. Let us study in brief about the types of monohydric alcohols. 1. Primary Alcohols Primary alcohols are those alcohols where the carbon atom of the hydroxyl group (OH) is attached to only one single alkyl group. Some examples of these primary alcohols include Methanol (propanol), ethanol, etc. The complexity of this alkyl chain is unrelated to the classification of any alcohol considered as primary. The existence of only one linkage among –OH group and an alkyl group and the thing that qualifies any alcohol as a primary. (RCH2OH)
  • 16. 2. Secondary Alcohols Secondary alcohols are those where the carbon atom of the hydroxyl group is attached to two alkyl groups on either side. The two alkyl groups present may be either structurally identical or even different. Some examples of secondary alcohols are given below. (R2CHOH)
  • 17. 3. Tertiary Alcohols Tertiary alcohols are those which feature a hydroxyl group attached to the carbon atom which is connected to 3- alkyl groups. The physical properties of these alcohols mainly depend on their structure. The presence of this -OH group allows the alcohols in the formation of hydrogen bonds with their neighboring atoms. The bonds formed are weak, and this bond makes the boiling points of alcohols higher than its alkanes. (R3CHOH ) Examples of tertiary alcohols include-
  • 19. As with other types of organic compounds, alcohols are named by both formal and common systems. The most generally applicable system is that adopted at a meeting of the International Union of Pure and Applied Chemist ry (IUPAC) in Paris in 1957. Using the IUPAC system, the name for an alcohol uses the -ol suffix with the name of the parent alkane, together with a number to give the location of the hydroxyl group. The rules are summarized in a three-step procedure:
  • 20. 1.The longest continuous chain (LCC) of carbon atoms containing the OH group is taken as the parent compound -- an alkane with the same number of carbon atoms. The chain is numbered from the end nearest the OH group. 2.The number that indicates the position of the OH group is prefixed to the name of the parent hydrocarbon, and the -e ending of the parent alkane is replaced by the suffix -ol. (In cyclic alcohols, the carbon atom bearing the OH group is designated C1, but the 1 is not used in the name.) Substituents are named and numbered as in alkanes. 3.If more than one OH group appears in the same molecule (polyhydroxy alcohols), suffixes such as -diol and -triol are used. In these cases, the -e ending of the parent alkane is retained.
  • 26.  Oxidation Reaction of Alcohol – Alcohols produce aldehydes and ketones on oxidation. The reaction is given below – C₂H₅OH + 2O CH₃COOH + H₂O Ethanol Ethanoic acid  Combustion of Alcohol – On heating ethanol gives carbon dioxide and water and burns with a blue flame. The reaction is given below – C₂H₅OH + 3O₂ 2CO₂ + 3H₂O → →
  • 27.  Dehydration of Alcohol – Alcohol can be dehydrated in an acidic medium. The removal of water molecules from a compound is called dehydration. Upon dehydration of alcohol alkenes are produced. The reaction is given below – C2H5OH (conc. H₂SO₄,▵)→C₂H₄ + H₂O  The reaction of Alcohol With Metal – Due to its acidic nature alcohol reacts with metal and forms alkoxide. For example, when ethanol reacts with sodium forms sodium ethoxide and hydrogen gas. The reaction is given below – 2C₂H₅OH + 2Na →2C₂H₅ONa + H₂
  • 28.  Formation of Halides From Alcohols – Alcohol reacts with HCl and forms alkyl halides by removal of hydroxyl groups. The reaction is given below ROH + HCl (Zn) → R-Cl + H₂  Esterification – Alcohol reacts with a carboxylic acid in presence of a catalyst and forms ester. It is called Fischer esterification. The reaction is given below – C₂H₅OH + C₂H5COOH →C₄H₈O₂ + H₂O
  • 31.  Alcohols are consumed as beverages where the alcohols specifically consist of 30–40 per cent of ethanol by volume.  These are used as an anti-freezing agent with a mixture of a solution containing ethylene glycol dissolved in water.  Alcohol ethanol is used as an antiseptic agent.  Some alcohols are used as fuels in internal combustion engines like the methanol.  In the field of medicine, a few of them are used as preservatives for the specimens in laboratories. Uses of Alcohols
  • 34. 1.What is alcohol? 2.What are the different types of alcohols? 3.Differentiate Monohydric, Dihydric, Trihydric and Polyhydric. 4.Differentiate Primary, Secondary and Tertiary alcohols. 5.What are the uses of alcohol?