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Organic chemistry

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Title: Organic chemistry


1
Organic chemistry
  • The carbon compounds

Prof. Paola Valentinis 2A- 2B
Scholastic year 2006/07
2
Glossary
Coal Organic Combustion Rocks plants Sweeteners Laboratory Soaps Term Chemist Theory Mysterious Fibres Phenomena inorganic
3
Organic chemistry
Fill in the blanks using the new words
Organic chemistry was the term applied originally
to the study of substances connected directly
with animals and plants, so it is derived from
the word organism. For this reason it received
the name organic. Such substances were thought to
contain a mysterius vital force wich made it
impossible for man to prepare them from inorganic
ingredients. But in 1828 the German chemist
Friedrich Wohler attempted to prepare crystals of
the inorganic salt ammonyum cyanate by
evaporating its solution . Istead, he obtained
crystals of urea an organic subtance already
known for 50 years an the main constituent of
urine. Over the following years further organic
substances were prepared in the laboratory and
eventually the vital force theory was
abandoned. Today the study of organic chemistry
is very important because it help us to
understand the phenomena living in the world.
Synthetic fibres, plastic, medicines, artificial
sweeteners are product of industrial organic
chemistry and the energy that man uses in every
industrial activity derives mainly from the
combustion of organic material found in coal an
crude oil.
4
carbon
  • The special role of carbon in the chemistry of
    the elements is the result of a combination of
    factors, including the number of valence
    electrons on a neutral carbon atom, the
    electronegativity of carbon, and the atomic
    radius of carbon atoms (see the table below).
  • The Physical Properties of Carbon
  • Electronic configuration 1s2 2s2 2p2
    Electronegativity 2.55 Covalent radius 0.077 nm
  • Carbon has four valence electrons 2s2 2p2 and
    it must either gain four electrons or lose four
    electrons to reach a rare-gas configuration. The
    electronegativity of carbon is too small for
    carbon to gain electrons from most elements to
    form C4- ions, and too large for carbon to lose
    electrons to form C4 ions. Carbon therefore
    forms covalent bonds with a large number of other
    elements, including the hydrogen, nitrogen,
    oxygen, phosphorus, and sulfur found in living
    systems.
  • Because they are relatively small, carbon atoms
    can come close enough together to form strong CC
    double bonds or even C C triple bonds. Carbon
    also forms strong double and triple bonds to
    nitrogen and oxygen. It can even form double
    bonds to elements such as phosphorus or sulfur
    that do not form double bonds to themselves

Even though organic chemistry focuses on
compounds that contain carbon and hydrogen, more
than 95 of the compounds that have isolated from
natural sources or synthesized in the laboratory
are organic.
5
Carbon and life
  • Several factors make carbon essential to
    life.
  • The ease with which carbon atoms form bonds to
    other carbon atoms.
  • The strength of C-C single bonds and the covalent
    bonds carbon forms to other non metals, such as
    N, O, P, and S.
  • The ability of carbon to form multiple bonds to
    other non metals, including C, N, O, P, and S
    atoms.
  • These factors provide an almost infinite variety
    of potential structures for organic compounds,
    such as vitamin C shown in the figure below.

6
hydrocarbons
  • Compounds that contain only carbon and hydrogen
    are known as hydrocarbons
  • Those that contain as many hydrogen atoms as
    possible are said to be saturated. The saturated
    hydrocarbons are also known as alkanes.
  • Carbon not only forms the strong C C single bonds
    found in alkanes, it also forms strong CC double
    bonds. Compounds that contain CC double bonds
    were once known as olefins (literally, "to make
    an oil") because they were hard to crystallize.
    (They tend to remain oily liquids when cooled.)
    These compounds are now called alkenes.
  • Alkenes are examples of unsaturated hydrocarbons
    because they have fewer hydrogen atoms than the
    corresponding alkanes

Compounds that contain C C triple bonds are
called alkynes. These compounds have four less
hydrogen atoms than the parent alkanes
7
Structure and Nomenclature of Hydrocarbons
The alkanes in the table above are all
straight-chain hydrocarbons, in which the carbon
atoms form a chain that runs from one end of the
molecule to the other. The generic formula for
these compounds can be understood by assuming
that they contain chains of CH2 groups with an
additional hydrogen atom capping either end of
the chain. Thus, for every n carbon atoms there
must be 2n 2 hydrogen atoms CnH2n2.
Because an alkene can be thought of as a
derivative of an alkane from which an H2 molecule
has been removed, the generic formula for an
alkene with one CC double bond is CnH2n.
8
pollution
  • Hydrocarbons are a
    precursor to ground-level ozone, a
    serious air pollutant in cities across the United
    States. A key component of smog, ground-level
    ozone is formed by reactions involving
    hydrocarbons and nitrogen oxides in the presence
    of sunlight. Hydrocarbon emissions result from
    incomplete fuel combustion and from fuel
    evaporation. Today's cars are equipped with
    emission controls designed to reduce both exhaust
    and evaporative hydrocarbons.

9
Try yourself synthetizes you an organic
mixtureMAKING SOAP FROM OLIVE OIL
  • INGREDIENTS125 cm3 of vegetable oil100 cm3 of
    water20 g of caustic soda (sodium
    hydroxide)salt (if required)essential oil or
    perfume (optional)

APPARATUSsafety gogglesbeakerglass rodmould
for setting soap
  • METHOD
  • Weigh out your caustic soda onto a folded piece
    of paper. DO NOT TOUCH IT.
  • Pour the oil and water into a big beaker and stir
    with a glass rod until you make an emulsion.
  • Carefully add the caustic soda, slowly and
    stirring all the time. DON'T TOUCH IT !
  • Keep stirring until a thick paste forms. This
    could take half an hour.
  • If you still don't have a paste after half an
    hour, stir in 4 spatulas of salt.
  • Add essential oil or perfume if you want.
  • Pour into mould and leave to set for a few days.
  • Keep your fingers crossed !

10
Lab- work
  • Write a purpose for the lab in you notebook.
    You might also wish to think about the following
    questions. They will help you prepare for the
    lab, but you need not turn them in at the
    beginning of class.
  • What reaction is described by the word
    saponification. What are the products from this
    reaction and what are the required reactants?
  • Draw out the full structure for three of the
    carboxylic acids listed in books table. Identify
    all of the polar bonds, and find the polar and
    non-polar regions of the molecule.
  • What is the most dangerous part of the lab?
  • Why is it critical to clean up all spills
    immediately?

11
bibliography
GCSE chemistry Complete Revision Practice
Roggi- Picking BIO-CHEM Zanichelli
www. thinkQuest.org
www.chemed.chem.purdue.edu.html
12
Thanks for your attentions
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