Post on 11-Jan-2016
LE 4-4
Hydrogen
(valence = 1)
Oxygen
(valence = 2)
Nitrogen
(valence = 3)
Carbon
(valence = 4)
LE 4-5
LengthEthane Propane
Butane 2-methylpropane(commonly called isobutane)
Branching
Double bonds
Rings
1-Butene 2-Butene
Cyclohexane Benzene
LE 4-7
Structural isomers differ in covalent partners, as shown in this example of two isomers of pentane.
Geometric isomers differ in arrangement about a double bond. In these diagrams, X represents an atom or group of atoms attached to a double-bonded carbon.
cis isomer: The two Xsare on the same side.
trans isomer: The two Xsare on opposite sides.
L isomer D isomer
Enantiomers differ in spatial arrangement around an asymmetric carbon, resulting in molecules that are mirror images, like left and right hands. The two isomers are designated the L and D isomers from the Latin for left and right (levo and dextro). Enantiomers cannot be superimposed on each other.
LE 4-10aa
STRUCTURE
(may be written HO—)
NAME OF COMPOUNDS
Alcohols (their specific names
usually end in -ol)
Ethanol, the alcohol present in
alcoholic beverages
FUNCTIONAL PROPERTIES
Is polar as a result of the
electronegative oxygen atom
drawing electrons toward itself.
Attracts water molecules, helping
dissolve organic compounds such
as sugars (see Figure 5.3).
LE 4-10ab
STRUCTURE
NAME OF COMPOUNDS
Ketones if the carbonyl group is
within a carbon skeleton
EXAMPLE
Acetone, the simplest ketone
A ketone and an aldehyde may
be structural isomers with
different properties, as is the case
for acetone and propanal.
Aldehydes if the carbonyl group is
at the end of the carbon skeleton
Acetone, the simplest ketone
Propanal, an aldehyde
FUNCTIONAL PROPERTIES
LE 4-10ac
STRUCTURE
NAME OF COMPOUNDS
Carboxylic acids, or organic acids
EXAMPLE
Has acidic properties because it isa source of hydrogen ions.
Acetic acid, which gives vinegarits sour taste
FUNCTIONAL PROPERTIES
The covalent bond betweenoxygen and hydrogen is so polarthat hydrogen ions (H+) tend todissociate reversibly; for example,
Acetic acid Acetate ion
In cells, found in the ionic form,which is called a carboxylate group.
LE 4-10ba
STRUCTURE
NAME OF COMPOUNDS
Amine
EXAMPLE
Because it also has a carboxyl
group, glycine is both an amine and
a carboxylic acid; compounds with
both groups are called amino acids.
FUNCTIONAL PROPERTIES
Acts as a base; can pick up a
proton from the surrounding
solution:
(nonionized)
Ionized, with a charge of 1+,under cellular conditions
Glycine
(ionized)
LE 4-10bb
STRUCTURE
(may be written HS—)
NAME OF COMPOUNDS
Thiols
EXAMPLE
Ethanethiol
FUNCTIONAL PROPERTIES
Two sulfhydryl groups can
interact to help stabilize protein
structure (see Figure 5.20).
LE 4-10bc
STRUCTURE
NAME OF COMPOUNDS
Organic phosphates
EXAMPLE
Glycerol phosphate
FUNCTIONAL PROPERTIES
Makes the molecule of which it
is a part an anion (negatively
charged ion).
Can transfer energy between
organic molecules.
Table 4.1 Functional Groups of Organic Compounds
LE 4-9
Estradiol
Testosterone
Male lion
Female lion
Common Elements found in living organisms
Molecular Composition of 2 cells
LE 5-2a
Short polymer Unlinked monomer
Dehydration removes a watermolecule, forming a new bond
Dehydration reaction in the synthesis of a polymer
Longer polymer
LE 5-2b
Hydrolysis adds a watermolecule, breaking a bond
Hydrolysis of a polymer
The molecules of life
• Carbohydrates (C,H,O)-monomer is a monosaccharide and polymers are polysaccharides
• Lipid-(C,H,O)-in triglycerides (polymer) the 2 monomers are glycerol and fatty acids. Steroids lipids are not monomers or polymers
• Proteins (C,H,O,N,S)-monomers are amino acids and the polymers are polypeptides
• Nucleic acids (C,H,O,N,P)-monomers are nucleotides and the polymers are polynucleotides.