Other Organic Compounds - UTM OpenCourseware
Transcript of Other Organic Compounds - UTM OpenCourseware
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Dr Nik Ahmad Nizam Bin Nik Malek, BSc (Ind. Chem.)(UTM), MSc (Chem)(UTM), PhD (Chem)(UTM), A.M.I.C
Senior Lecturer,
Department of Biotechnology and Medical Engineering
Faculty of Biosciences and Medical Engineering
Other Organic Compounds
BIO-ORGANIC CHEMISTRY (Organic Chemistry for Biology Students)
(SQBS 1603)
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Other Functional Groups
• Alkyl halides – Organic molecules containing halogen atom
• F, Cl, Br and I
• Organic compounds that contain sulfur (S) – Thiol group: Sulfhydryl group
– Disulfide Bridge
• Organic compounds that contain fosforus (P) – Phosphate
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Alkyl Halides
The haloalkanes: Halo-group
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• Classification
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C X Alkyl halide X = F, Cl, Br, I
C
H
X
H
R C
H
X
R'
R C
R''
X
R'
R
Primary (1)
Secondary (2)
Tertiary (3)
Alkyl Halides
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Naming Alkyl Halides • Give the IUPAC name of the following alkyl halide
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Cl
H3C
H2C
CH
CH3
H2C
CH2
CH
Cl
CH3
7 C’s : heptane
1
2
3
4
5
6
7
Cl (Chloro) at C2
Methyl at C5
2-chloro-5-methylheptane
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Halogenation
• The addition of halogen (X2) to an alkene
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C C X X C
X
C
XX = Cl or Br
Alkene Alkyl dihalide
C C
H
H H
H
Cl2 C
Cl
H
CH H
Cl
H
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Hydrohalogenation
• The addition of HX (X = Cl or Br) to an alkene
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C C H-X C
H
C
XX=Cl or Br
C C
H
H H
H
HCl C
H
H
CH H
Cl
H
Alkene Alkyl halide
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Hydrohalogenation
• Markovnikov’s rule
– In the addition of HX to an unsymmetrical
alkene, the H atom bonds to the less
substituted carbon atom
The carbon that has more H’s to begin with.
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Hydrohalogenation
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C C
H
H3C H
H
HCl C
H
H
CH3C H
Cl
H
C
Cl
H
CH3C H
H
H
or
1-Chloro-propanePropene
2-Chloro-propane
C C
H
H3C H
H
According to Markovnikov’s rule
the H atom bonds to the less substituted carbon atom (has more H’s )
Only product
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Thiols
• Thiols group: organic compounds that
contain a sulfhydryl group
– SH group
– Similar to alcohol (OH group)
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S
H
O
H
Hydroxyl Thiol
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Naming Thiols
• Name the parent hydrocarbon as an
alkane and add the suffix –thiol.
• Number the carbon chain to give the SH
group the lower number
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SH
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SH
1 2
3 4
5
5 C’s : pentane
Thiol at C2
methyl at C3 and C4
3,4-dimethyl-2-pentanethiol
Naming Thiols
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Physical properties of thiols
• Sulfur is only as electronegative as carbon
– Thus, thiol group does not have the same
functionality than molecules containing oxygen
(alcohol, ether, ester etc) or nitrogen (amide
and amine).
– Non-polar molecule.
– Hydrogen bonding is impossible.
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Disulfide Bridge
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S
H H
S
S S
Two neighboring thiol groups can join
together
Disulfide bridge
disulfide bridge have a vital role in stabilizing the structure of proteins. It firmly linking together amino acids from different parts of the protein to help “lock” the protein in the place.
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Phosphate
• phosphate (ionized form)
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OP-O
O
O-
PO43-
Phosphate ion
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• Phosphate in biological compounds
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Adenosine triphosphate (ATP)
Phosphate
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REFERENCES
• Crowe, J., Bradshaw, T. and Monk, P. (2006), Chemistry for the Biosciences: The Essential Concepts, Oxford University Press, Oxford.
• Horton, H.R., Moran, L.A., Scrimgeour, K.G., Perry, M.D. and Rawn J.D. (2006). Principles of Biochemistry, 4th Edition. Pearson International Edition.
• Smith, J.G. (2010). General, Organic and Biological Chemistry. McGraw-Hill Higher Education.
• Denniston, K.J., Toping, J.J. and Caret, R.L. (2008). General, Organic and Biochemistry, 6th edition. McGraw-Hill Higher Education.
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MY PROFILE
Dr Nik Ahmad Nizam Bin Nik Malek,
BSc (Ind. Chem.)(UTM), MSc (Chem)(UTM), PhD (Chem)(UTM), A.M.I.C Senior Lecturer,
Department of Biotechnology and Medical Engineering,
Faculty of Biosciences and Medical Engineering,
Universiti Teknologi Malaysia.
Email: [email protected], [email protected]
Website: http://www.staff.blog.utm.my/niknizam/