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Introduction to Organic Chemistry

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Title: Introduction to Organic Chemistry


1
Introduction to Organic Chemistry
  • CHEM 2124 General Chemistry II
  • Alfred State College
  • Professor Bensley

2
Learning Objectives
  • Recognize the characteristic features of organic
    compounds.
  • Predict the shape around atoms in organic
    molecules.
  • Use shorthand notation to draw organic molecules.
  • Recognize the common functional groups and
    understand their importance.

3
Learning Objectives
  • Distinguish organic compounds from ionic
    inorganic compounds.
  • Determine whether or not an organic compound is
    polar or non-polar.
  • Determine solubility properties of organic
    compounds.

4
I. Introduction to Organic Chemistry
Organic chemistry is the study of compounds
that contain the element carbon.
5
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6
II. Characteristics of Organic Compounds
  • All organic compounds contain carbon atoms and
  • most contain hydrogen atoms.
  • Carbon forms single, double, and triple bonds to
  • other carbon atoms.
  • Some compounds have chains of atoms and some
  • compounds have rings.

7
II. Characteristics of Organic Compounds
4. Organic compounds may also contain elements
other than carbon and hydrogen.
THE RULE OF HONC
8
III. Drawing Organic Molecules
A. Condensed Structures
  • Some bond lines can be drawn in for effect or to
  • show specific bonding.

9
III. Drawing Organic Molecules
A. Condensed Structures
  • Identical groups can be condensed further

10
III. Drawing Organic Molecules
B. Skeletal Structures
11
IV. Functional Groups
A. Hydrocarbons
  • Alkanes
  • Alkenes
  • Alkynes
  • Aromatics

B. Compounds Containing a Single Bond to a
Heteroatom
C. Compounds Containing a CO (Carbonyl) group
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13
V. Properties of Organic Compounds
14
V. Properties of Organic Compounds
A. Polarity
  • A covalent bond is nonpolar when two atoms of
  • identical or similar electronegativity are
    bonded.
  • If the individual polar
  • bonds (dipoles) cancel
  • in a molecule, the
  • molecule is nonpolar.
  • If the individual bond
  • dipoles do not cancel, the
  • molecule is polar.

15
V. Properties of Organic Compounds
B. Solubility
  • The rule of solubility is like dissolves like.

CH3CH2OH ethanol
CH3CH2CH2CH2CH2CH3 hexane
  • small polar molecule
  • O atom present
  • H2O soluble
  • organic solvent soluble
  • small nonpolar molecule
  • no O or N present
  • H2O insoluble
  • organic solvent soluble

cholesterol
16
VI. Shapes of Organic Molecules
VSEPR theory The most stable arrangement
keeps the groups on a central atom as far away
from each other as possible.
17
VI. Shapes of Organic Molecules
To draw a 3-D tetrahedron in 2-D, we use
  • a solid line for bonds in the plane
  • a wedge for a bond in front of the plane
  • a dashed line for a bond behind the plane
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