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BY Dr. EKHLAQUE
ekhlaquebiotech@gmail.com
Functional groups give specific properties
found together in a variety of different molecules.
Each functional group has specific properties that,
when attached to a larger molecule, in turn give
the larger molecules specific properties.
several functional groups in biology, including
alcohols, aldehydes, ketones, acids, amines,
phosphates, and thiols.
 An important biological molecules containing functional
groups is the amino acids, which have both a carboxyl group
and an amino group attached to the same carbon atom, called
the α carbon.
 Also attached to the α carbon atom are a hydrogen atom and a
side chain, or R group
 Different side chains have different chemical compositions,
structures, and properties.
 Each of the 20 amino acids found in proteins has a different
side chain that gives it its distinctive chemical properties.
 Because they possess both carboxyl and amino groups, amino
acids are simultaneously acids and bases.
Isomers have different arrangements of the
same atoms
Isomers are molecules that have the
same chemical formula but different
arrangements of the atoms.
(The prefix iso- meaning “same,”).
we will consider two: structural
isomers and optical isomers.
Structural isomers
It differ in how their atoms are joined together.
Consider two simple molecules, each composed
of 4 carbon and 10 hydrogen atoms bonded
covalently, both with the formula C4H10.
These atoms can be linked in two different ways,
resulting in two forms of the molecule:
Optical isomers
 The carbon atom has four different atoms or groups
attached to it.
This pattern allows two different ways of making the
attachments, each the mirror image of the other.
Such a carbon atom is an asymmetrical carbon, and the
pair of compounds are optical isomers of each other.
You can imagine your right and left hands as optical
isomers.
Just as a glove is specific for a particular hand, some
biochemical molecules can interact with one optical
isomer of a compound, but are unable to “fit” the other.
Cont…
The α carbon in an amino acid is an asymmetrical
carbon because it is bonded to four different
functional groups.
Therefore, amino acids exist in two isomeric
forms, called D-amino acids and L-amino acids.
D and L stand for right (dextro) and left (levo),
respectively.
Only L-amino acids are commonly found in most
organisms, and their presence is an important
chemical “signature” for life.
Molecules vary in size
Some are small, such as H2 and CH4.
Others are larger, such as a molecule of table
sugar (Sucrose, C12H22O11), which has 45
atoms.
Still other molecules, especially proteins
such as hemoglobin, are gigantic, sometimes
containing tens of thousands of atoms.
Functional group in Biiology

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Functional group in Biiology

  • 2. Functional groups give specific properties found together in a variety of different molecules. Each functional group has specific properties that, when attached to a larger molecule, in turn give the larger molecules specific properties. several functional groups in biology, including alcohols, aldehydes, ketones, acids, amines, phosphates, and thiols.
  • 3.
  • 4.  An important biological molecules containing functional groups is the amino acids, which have both a carboxyl group and an amino group attached to the same carbon atom, called the α carbon.  Also attached to the α carbon atom are a hydrogen atom and a side chain, or R group  Different side chains have different chemical compositions, structures, and properties.  Each of the 20 amino acids found in proteins has a different side chain that gives it its distinctive chemical properties.  Because they possess both carboxyl and amino groups, amino acids are simultaneously acids and bases.
  • 5. Isomers have different arrangements of the same atoms Isomers are molecules that have the same chemical formula but different arrangements of the atoms. (The prefix iso- meaning “same,”). we will consider two: structural isomers and optical isomers.
  • 6. Structural isomers It differ in how their atoms are joined together. Consider two simple molecules, each composed of 4 carbon and 10 hydrogen atoms bonded covalently, both with the formula C4H10. These atoms can be linked in two different ways, resulting in two forms of the molecule:
  • 7. Optical isomers  The carbon atom has four different atoms or groups attached to it. This pattern allows two different ways of making the attachments, each the mirror image of the other. Such a carbon atom is an asymmetrical carbon, and the pair of compounds are optical isomers of each other. You can imagine your right and left hands as optical isomers. Just as a glove is specific for a particular hand, some biochemical molecules can interact with one optical isomer of a compound, but are unable to “fit” the other.
  • 8.
  • 9. Cont… The α carbon in an amino acid is an asymmetrical carbon because it is bonded to four different functional groups. Therefore, amino acids exist in two isomeric forms, called D-amino acids and L-amino acids. D and L stand for right (dextro) and left (levo), respectively. Only L-amino acids are commonly found in most organisms, and their presence is an important chemical “signature” for life.
  • 10.
  • 11. Molecules vary in size Some are small, such as H2 and CH4. Others are larger, such as a molecule of table sugar (Sucrose, C12H22O11), which has 45 atoms. Still other molecules, especially proteins such as hemoglobin, are gigantic, sometimes containing tens of thousands of atoms.