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Transcript
More Organic
Today
Review hydrocarbons
Functional Groups
Condensation Reaction
Biopolymers
Principles of Chemistry II
© Vanden Bout
How many carbons and hydrogens in the following?
A.
6 C, 14 H
B.
6 C, 15 H
C. 6 C, 16 H
D. 7 C, 15 H
E.
3H
1H
1H
2H
1H
3H
3H
7 C, 14 H
Principles of Chemistry II
© Vanden Bout
Other side-chains
Halogens
F Fluoro
Cl Chloro
Br Bromo
I Iodo
OH group
hydroxy
NH2 group
amino
Benzene Ring
phenyl
Principles of Chemistry II
© Vanden Bout
Cyclic Hydrocarbons
the carbon chain connects back to itself
cyclobutane
Principles of Chemistry II
© Vanden Bout
Structural Isomers
hexane (C6H14)
doc cam
Principles of Chemistry II
© Vanden Bout
Nomenclature with functional group
Put the number by before the functional group suffix
you'll be tested on this one
you'll be
understood
IUPAC
name
1 butene
but-1-ene
Principles of Chemistry II
© Vanden Bout
Name this compound
A.
2-methyl pent-5-ene
B.
2-methyl hex-3-ene
C. 1,1-dimethyl pent-2-ene
D. 5-methyl hex-3-ene
E.
5-methyl hex-4-ene
Principles of Chemistry II
© Vanden Bout
Dienes
Two double bonds
5 carbon chain, parent
penta
no side chains
two double bonds diene
position 1 and 3
penta-1,3-diene
Principles of Chemistry II
© Vanden Bout
Alkyne
Carbon Carbon Triple Bond
Suffix -yne
6
5
4
3
2
1
2 methyl hex-3-yne
Principles of Chemistry II
© Vanden Bout
Other functional groups
Common
Ethanol
R OH
R = Generic representation
of the rest of the molecule
functional group
-OH group is an alcohol
suffix is -ol
Principles of Chemistry II
© Vanden Bout
Name this compound
OH
A. heptan-2-ol
B.
hexan-4-ol
C. 2-ethylbutan-1-ol
D. 2-ethylpentan-1-ol
E. hexan-3-ol
Principles of Chemistry II
© Vanden Bout
Ketone
R
O
C
Common
Acetone
(nail polish remover)
R
carbon double bonded to an oxygen
bonded to carbons on either side
suffix is -one
Principles of Chemistry II
© Vanden Bout
Which of the following is a ketone?
O
H
A
O
O
O
B
C
A. A
B.
B
C. C
butan-3-one
D. A & B
E. all three
Principles of Chemistry II
© Vanden Bout
Aldehyde
R
O
C
Common
Formaldehyde
(Fetal Pig Storage)
H
carbon double bonded to an oxygen
bonded to carbon on one side
(like a ketone at the end of a chain)
suffix is -al
Principles of Chemistry II
© Vanden Bout
Name this compound
H
O
A. hex-3-enal
B.
hex-3-en-1-al
C. hex-3-en-6-al
D. hex-6-al-3-ene
E. hexene6-3-al
Principles of Chemistry II
No need to number aldehyde
its always at the end
H shown to emphasize the
functional group
© Vanden Bout
Carboxylic Acid
R
O
C
Common
Acetic Acid
(vinegar)
OH
carbon double bonded to an oxygen
bonded to carbon on one side
OH on the other side
suffix is -oic acid
Principles of Chemistry II
© Vanden Bout
Name this compound
O
OH
A. methanoic acid
B.
No need to number carboxylic acid
its always at the end
ethanoic acid
C. propanoic acid
this compound is also
commonly known as acetic acid
D. 3 hydroxy propan-2-one
E. propanol
Principles of Chemistry II
© Vanden Bout
Ester
R
O
C
Common
lots of flavorings
O R'
carbon double bonded to an oxygen
bonded to carbon on one side
OR on the other side
suffix is -oic acid
Principles of Chemistry II
© Vanden Bout
Name this compound
O
O
A. ethyl butanoate
B.
butyl methanoate
C. methyl heptanoate
D. butyl ethanoate
No need to number ester
name the two sides
part with the carboxyl (C=O)
is the parent
other part is like the side chain
E. pentyl ethanoate
Principles of Chemistry II
© Vanden Bout
Ether
R
O
Diethyl Ether
(knocks you out)
R'
carbon oxygen in the middle of the chain
suffix is -ether
Principles of Chemistry II
© Vanden Bout
O
Treat as two "side chains"
methyl ethyl ether
Principles of Chemistry II
© Vanden Bout
Primary Amine
R NH2
-NH2 group is an amine
suffix is -amine
Principles of Chemistry II
© Vanden Bout
Amide
R
O
C
R"
N R'
carbon double bonded to an oxygen
bonded to carbon on one side
N on the other side
suffix is -amide
Principles of Chemistry II
© Vanden Bout
Naming amide
Treat part with C=O as parent
parts on the N as sidechains
O
pentanamide
NH2
O
N-ethyl-N-methylpentanamide
N
Principles of Chemistry II
© Vanden Bout
NH2
O
Amine
Ether
O
Ketone
O
Amide
N
Principles of Chemistry II
© Vanden Bout
OH
OH
O
Alcohol
Carboxylic Acid
OH
O
Ester
O
Alkene
Principles of Chemistry II
© Vanden Bout
Important Reaction for Biochemistry
Formation of an Amide
The don't call them functional groups for nothing
Carboxylic Acid
Primary Amine
O
R
C
OH
Principles of Chemistry II
H
N
R'
H
© Vanden Bout
Carboxylic Acid
Primary Amine
O
R
C
OH
H
N
R'
H
O
H
C N
R
R' + H2O
Amide + Water
Principles of Chemistry II
© Vanden Bout
Amino Acid
O
H2N
C
C
OH
R
Carboxylic End and Amine End
Can react with itself
(or similar molecules) in a chain
Principles of Chemistry II
© Vanden Bout
Polypeptide
Two distinct ends
N-terminus is an amine
C-terminus is a carboxylic acid
Principles of Chemistry II
© Vanden Bout
Carboxylic Acid
Alcohol
O
R
C
OH
O
R'
H
O
C O
R
R' + H2O
Ester + Water
Principles of Chemistry II
© Vanden Bout
Triglycerides
Fatty Acid
(carboxylic acid with long chain)
Gylcerol
HO
OH
C12H25COOH
OH
O
C12H25CO
O
OCC12H25
O
OCC12H25
Makes Trigylceride
Principles of Chemistry II
© Vanden Bout
The three fatty acids can
all be the same or different
High levels of triglycerides is linked to
build up of plaque in the arteries
= heart disease
Principles of Chemistry II
© Vanden Bout
Alcohol
R
Alcohol
OH
R
O
HO
R'
R' + H2O
Ether + Water
Principles of Chemistry II
© Vanden Bout
Sugars
Glucose
(key factor for sugars lots of hydroxyls)
They can react to form chains of sugars
polysaccharide
Principles of Chemistry II
© Vanden Bout
Celluose
Very long ether chain
(pretty much all plant material)
Principles of Chemistry II
© Vanden Bout
Condensation Reactions
(two molecules make one + water)
Carboxylic Acid + Amine = Amide + water
Carboxylic Acid + Alcohol = Ester + water
Alcohol + Alcohol = Ether + water
Principles of Chemistry II
© Vanden Bout