By: IZZATI, RAUDAH, WAN ALIA.
10.1 COMPARE THE SIMILARITIES AND
 DIFFERENCES IN THE STRUCTURE OF THE
         NATURAL PIGMENTS:
ANTHOCYANINS, CAROTENOIDS, CHLOROP
           HYLL AND HEME
Anthocyanins.
Carotenoids.
Chlorophyll.
Heme.
SIMILARITIES
• BETWEEN HEME AND CHLOROPHYLL
- Contain a planar heterocyclic unit called a
  porphin whose structure contain a cyclic
  system of conjugated double bonds.
- Porphins with substituents in positions 1 to 8
  are called porphyrins.
Resonance structure of porphine




 Conjugate double bonds is possible by means of alternating single and
 double bond.
DIFFERENCES
ANTHOCYANIN           CAROTENOID             CHLOROPHYLL             HEME
1. Has a C6C3C6      1. Derived from a       1. 2 types of           1. Hemoglobin
skeleton with 2      40-carbon polyene       chlorophyll:            contains 4 heme
conjugated benzene chain.                    -chlorophyll a: blue-   subunits while
rings isolated by an                         green                   myoglobin contains
oxygen-containing                            -chlorophyll b :        one heme ring
pyran ring.                                  yellow-green

2. Always have a      2. May be              2. Chlorophyll b        2. A haemoglobin
sugar residue at      terminated by cyclic   differs from            molecule contains 4
position 3 and        end-groups and         chlorophyll a by        protein chains
glucose occur at      may be                 having an aldehyde      while myoglobin
position 5,7,3’ and   complemented           (-CHO) group in         molecule contains
4’.                   with oxygen            placed of a methyl      one protein chain
                      containing             group
                      functional groups.     (-CH3).
3. It is porphyrin   3. Each heme ring
pigments,            contains one iron
composed of 4        ( II) ion
pyrrole ring to form
tetrapyrrole with
magnesium ion
complex in the
centre of the ring.
                    4. The iron in the
                    heme group is
                    coordinated to the
                    four nitrogen atoms
                    in the prophyrin
                    ring and also to a
                    nitrogen atom from
                    the histidine
                    residue of the
                    hemoglobin protein
                    known as the globin
5. The 6 position
around the iron of
the heme is
occupied by oxygen
when the
haemoglobin
protein is
oxygenated
10.2 EXPLAIN WHY
ANTHOCYANINS, CAROTENOIDS, CHLOROP
    HYLL AND HEME GROUP FORM
  COLOURED COMPOUND WHILE MANY
   OTHERS ORGANIC MOLECULES ARE
           COLOURLESS.
a) Chromophores are unsaturated groups of atoms in
   organic compounds whose electron absorb
   radiation in the visible and ultraviolet region of the
   electromagnectic spectrum.
b) The wavelength of light absorb by different
   chromophores are characteristic of the
   chromophores and can be used for their
   identification.
c) They can change with temperature, solvent, extend
   of conjugation and the presence of saturated
   groups.
d) Anthocyanins
• The absorbance spectrum is similar with
  cyanidin.
• Cyanidin is the parent compound of the
  anthocyanins but lacks of glucose residue.
• Under acidic conditions (low pH) cynidin is
  red.
• Graph




• The absorbance at 375 nm lies in the UV region of the electromagnetic
  spectrum so it has no effect on the observed colour f cyaniding
• But, the absorbance at the 530 nm lies in the blue-green region of the
  visible spectrum hence cyaniding transmits the complementary colour
  of the eye, namely red.
• Although the absorbance spectra of anthocyanins will be similar with
  cyanidin but it will vary with due to the presence of differential
  functional group.
• The colours of anthocyanins will also vary with temperature and pH
  due to the presence of forms in equilibrium.
e) In Carotenoids and Chlorophyll
• Different molecule absorb light at different wavelength
   because of differences in their electronic structures.




• Figure 2 shows the absorption spectra of the two closely
  related chlorophylls (a and b) and carotenoid found in plant.
• It is the electronic arrangement of a molecule that is responsible for
  the absorption of light in the ultraviolet and visible region of the
  electromagnetic spectrum.
• It is the electron in the molecule that are largely responsible for
  the absorption of light in the visible.
• A bond consist of two electron in a spin pair arrangement-one
  electron spins clockwise and the other spins anticlockwise.
• The total potential energy increases as a result of absorption of
  light.
• The absorption of light by electron in a bond can be viewed in
  terms of an energy level diagram. (Figure 3)

                                        *


                                      hf (photon)

                           Figure 3
• The diagram shows the light wave (photons) as a
  squiggly arrow.
• One of the electron and has absorbed this
  energy and moved from the ground state( ) to an
  excited state ( *).
• Now the two electrons will no longer have
  complementary spins.
• This energy jumped occurs only when light of
  exactly the right wavelength (energy) is absorbed.
• The reflected light will have a different energy
  from the incident light and will have a different
  colour.
f) Heme
• As the heme group is in red colour so the
   intensity of absorption of electron is high at
   the blue-green region of visible
   electromagnetic. spectrum.
• Therefore the reflected light is red in colour.
10.3 DEDUCE WHETHER ANTHOCYANINSAND
  CAROTENOIDS ARE WATER SOLUBLE OR
   FAT SOLUBLE FROM THEIR STRUCTURE.
Natural pigment        Explaination



                       -freely soluble in water but
                       poorly soluble in non-polar
                       organic solvents
                       -presence of 1 or more residues
                       helps the anthocyanins
                       maintains its solubility in water.
        Anthocyanins   -the sugar residue contain 1 or
                       more OH- group which can
                       hydrogen bond with water
                       molecules.
                       -if sugar is hydrolyse, the
                       solubility decreases.
Natural pigment         Explaination


                        -poorly soluble in water but freely
                        soluble in non-polar organic solvent
                        because it is essentially hydrocarbon
                        in nature of the solvent.
                        -the polar functional groups
                        outweighed by the much larger
                        polyene backbone, which is
          Carotenoids   hydrophobic.
                        -dissolving carotenoid in water would
                        be an energetically unfavoured
                        process as hydrogen bond between
                        water molecules would be replaced
                        by VDW
                        -carotenoids that are soluble in water
                        contains carboxylic functional group.
THANK YOU 

Presentation organic chem

  • 1.
  • 2.
    10.1 COMPARE THESIMILARITIES AND DIFFERENCES IN THE STRUCTURE OF THE NATURAL PIGMENTS: ANTHOCYANINS, CAROTENOIDS, CHLOROP HYLL AND HEME
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
    SIMILARITIES • BETWEEN HEMEAND CHLOROPHYLL - Contain a planar heterocyclic unit called a porphin whose structure contain a cyclic system of conjugated double bonds. - Porphins with substituents in positions 1 to 8 are called porphyrins.
  • 8.
    Resonance structure ofporphine Conjugate double bonds is possible by means of alternating single and double bond.
  • 9.
    DIFFERENCES ANTHOCYANIN CAROTENOID CHLOROPHYLL HEME 1. Has a C6C3C6 1. Derived from a 1. 2 types of 1. Hemoglobin skeleton with 2 40-carbon polyene chlorophyll: contains 4 heme conjugated benzene chain. -chlorophyll a: blue- subunits while rings isolated by an green myoglobin contains oxygen-containing -chlorophyll b : one heme ring pyran ring. yellow-green 2. Always have a 2. May be 2. Chlorophyll b 2. A haemoglobin sugar residue at terminated by cyclic differs from molecule contains 4 position 3 and end-groups and chlorophyll a by protein chains glucose occur at may be having an aldehyde while myoglobin position 5,7,3’ and complemented (-CHO) group in molecule contains 4’. with oxygen placed of a methyl one protein chain containing group functional groups. (-CH3).
  • 10.
    3. It isporphyrin 3. Each heme ring pigments, contains one iron composed of 4 ( II) ion pyrrole ring to form tetrapyrrole with magnesium ion complex in the centre of the ring. 4. The iron in the heme group is coordinated to the four nitrogen atoms in the prophyrin ring and also to a nitrogen atom from the histidine residue of the hemoglobin protein known as the globin
  • 11.
    5. The 6position around the iron of the heme is occupied by oxygen when the haemoglobin protein is oxygenated
  • 12.
    10.2 EXPLAIN WHY ANTHOCYANINS,CAROTENOIDS, CHLOROP HYLL AND HEME GROUP FORM COLOURED COMPOUND WHILE MANY OTHERS ORGANIC MOLECULES ARE COLOURLESS.
  • 13.
    a) Chromophores areunsaturated groups of atoms in organic compounds whose electron absorb radiation in the visible and ultraviolet region of the electromagnectic spectrum. b) The wavelength of light absorb by different chromophores are characteristic of the chromophores and can be used for their identification. c) They can change with temperature, solvent, extend of conjugation and the presence of saturated groups.
  • 14.
    d) Anthocyanins • Theabsorbance spectrum is similar with cyanidin. • Cyanidin is the parent compound of the anthocyanins but lacks of glucose residue. • Under acidic conditions (low pH) cynidin is red.
  • 15.
    • Graph • Theabsorbance at 375 nm lies in the UV region of the electromagnetic spectrum so it has no effect on the observed colour f cyaniding • But, the absorbance at the 530 nm lies in the blue-green region of the visible spectrum hence cyaniding transmits the complementary colour of the eye, namely red. • Although the absorbance spectra of anthocyanins will be similar with cyanidin but it will vary with due to the presence of differential functional group. • The colours of anthocyanins will also vary with temperature and pH due to the presence of forms in equilibrium.
  • 16.
    e) In Carotenoidsand Chlorophyll • Different molecule absorb light at different wavelength because of differences in their electronic structures. • Figure 2 shows the absorption spectra of the two closely related chlorophylls (a and b) and carotenoid found in plant.
  • 17.
    • It isthe electronic arrangement of a molecule that is responsible for the absorption of light in the ultraviolet and visible region of the electromagnetic spectrum. • It is the electron in the molecule that are largely responsible for the absorption of light in the visible. • A bond consist of two electron in a spin pair arrangement-one electron spins clockwise and the other spins anticlockwise. • The total potential energy increases as a result of absorption of light. • The absorption of light by electron in a bond can be viewed in terms of an energy level diagram. (Figure 3) * hf (photon) Figure 3
  • 18.
    • The diagramshows the light wave (photons) as a squiggly arrow. • One of the electron and has absorbed this energy and moved from the ground state( ) to an excited state ( *). • Now the two electrons will no longer have complementary spins. • This energy jumped occurs only when light of exactly the right wavelength (energy) is absorbed. • The reflected light will have a different energy from the incident light and will have a different colour.
  • 19.
    f) Heme • Asthe heme group is in red colour so the intensity of absorption of electron is high at the blue-green region of visible electromagnetic. spectrum. • Therefore the reflected light is red in colour.
  • 20.
    10.3 DEDUCE WHETHERANTHOCYANINSAND CAROTENOIDS ARE WATER SOLUBLE OR FAT SOLUBLE FROM THEIR STRUCTURE.
  • 21.
    Natural pigment Explaination -freely soluble in water but poorly soluble in non-polar organic solvents -presence of 1 or more residues helps the anthocyanins maintains its solubility in water. Anthocyanins -the sugar residue contain 1 or more OH- group which can hydrogen bond with water molecules. -if sugar is hydrolyse, the solubility decreases.
  • 22.
    Natural pigment Explaination -poorly soluble in water but freely soluble in non-polar organic solvent because it is essentially hydrocarbon in nature of the solvent. -the polar functional groups outweighed by the much larger polyene backbone, which is Carotenoids hydrophobic. -dissolving carotenoid in water would be an energetically unfavoured process as hydrogen bond between water molecules would be replaced by VDW -carotenoids that are soluble in water contains carboxylic functional group.
  • 23.