Organic Chemistry Organic Chemistry Historically the distinction between inorganic and organic substances was based on whether or not they were produced by living systems It was believed that some sort of life force was needed to synthesize them ID: 647333
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Slide1
Organic Chemistry
The study of carbon-based compounds and their properties.Slide2
Organic ChemistrySlide3
Organic ChemistrySlide4
Historically the distinction between inorganic and organic substances was based on whether or not they were produced by living systems. It was believed that some sort of “life force” was needed to synthesize them.
Organic ChemistrySlide5
In 1828, the German chemist Freidrich Wohler (1800-1882) prepared urea from the inorganic salt ammonium cyanate by simple heating.
NH
4
OCN
H
2
N—C—NH
2
O
urea
however...Slide6
Hydrocarbons:
contain only hydrogen and carbon
Hydrocarbons
Aliphatic
Aromatic
Alkanes Alkenes Alkynes Cyclic
Hydrocarbons can be divided into different types, depending on their bonding.Slide7
Naming Organic Molecules
Alkanes
- - Carbon chain, no double or triple bonds. All
single bonds
(saturated)
Alkenes
- - Carbon chain, contains
double bond
(s)
(unsaturated)
Alkynes
- - Carbon chain, contains
triple bond
(s) (unsaturated)Slide8
Naming Organic Molecules
There are two parts to the main name of each molecule…
prefix: tells the # of carbons in main chain or ring
suffix: tells the type of bonding in the chain or ringSlide9
Prefix:
indicates number of carbon atoms in the main chain or ring
meth-
eth-
prop-
but-
pent-
6 hex-
7 hept-
oct-
non-
dec-Slide10
Suffix:
indicates types of bonds present
Alkanes: (all single bonds) ___ -ane
Alkenes: (double bond) ___ -ene
Alkyne: (triple bond) ___ -yneSlide11
Saturated Hydrocarbons: the
ALKANES
:
chains of carbon connected by single bonds:
contain only single C-C bondsSlide12
Saturated v. Unsaturated fats
Saturated
with
H
Single bonds
are free to
rotate, so
these fats
can pack
tightly
(solid @
room temp)Slide13
Which one is saturated?Slide14
For a bit of a demonstration…Good Eats fat train analogy
Watch episode from 1:30 to 5:00Slide15
ALKANESSlide16
ALKANESSlide17
ALKANESpropane, C3H
8Slide18
ALKANESbutane, C4H
10Slide19
ALKANESpentane, C5H
12Slide20
ALKANEShexane, C6H
14Slide21
ALKANESoctane, C8H
18Slide22
Don’t write this example down, but watch to see where we’re going with this…Slide23
(Although you will be required to include the H’s if you take IB Chemistry)Slide24Slide25Slide26
“Normal” v. Branched“normal” hydrocarbons are straight chains; no branching
Branched-chain hydrocarbons – isomers of “normal” hydrocarbons; have same formula, but different structuresSlide27
n-butaneSlide28
2-methlypropaneSlide29
n-pentaneSlide30
2-methylbutaneSlide31
Are there any other pentane isomers?Slide32
Another branched alkane: 2,2-dimethylpentaneSlide33
cyclopentane
CycloalkanesSlide34
CycloalkanescyclobutaneSlide35
Cycloalkanes________________________
m
ethyl-
e
thyl-
1
2
3
3
2
1
green
or
red
?
-ethyl- -
methylcyclopentane
1
3Slide36
Unsaturated Hydrocarbons: ALKENES – contain C-C double bonds
2-penteneSlide37
Unsaturated Hydrocarbons: ALKENES – contain C-C double bonds
2,4-hexadieneSlide38
Unsaturated Hydrocarbons: ALKYNES – contain C-C triple bonds
1-butyneSlide39
Unsaturated Hydrocarbons: ALKYNES – contain C-C triple bonds
3-ethyl-1-pentyneSlide40
Aromatic Hydrocarbons:
benzene
– the simplest aromatic hydrocarbon; has a symmetrical ring structureSlide41
Aromatic Hydrocarbons:
benzene
– can be drawn like this…Slide42
Derivatives of benzene:
1-ethyl-2-methylbenzeneSlide43
Derivatives of benzene:
1,2-dimethyl-4-propylbenzeneSlide44
For your homework:
If a halogen is attached, use the following prefixes:
fluoro
-
chloro
-
bromo
- iodo-
(instead of methyl-, ethyl-, propyl-, etc.)