Title: Organic Chemistry
1Organic Chemistry
2Syllabus
- How to contact me?
- Exams.
- Grading policy.
- Lecture schedule.
- Homework problems.
- Tutoring center, K-211.
3Why study organic chemsitry?
Page 256
the fundamental processes of organic
chemistry are the same in the living cell
4Topics you should know from General Chemistry
- Atom - Orbitals (s p) and electronic
configuration. - Molecule - Covalent bonding, Lewis structure,
octet rule, molecular orbital (?, ?, ?, ?),
hybridization (sp3, sp2,sp), geometry (planar,
Td), formal charge, empirical formula, isomers,
dipole moment, molecular bond, resonance
structure. - Intermolecular Forces - dipole-dipole, van der
Waal dispersion, hydrogen bonding. - Acid-Base - Definitions, pH, Ka, pKa, acid
strength, structure and acidity. - Kinetics - Rates, rate law, Ea, activated
(transition state) complex, intermediate,
reaction mechanism, molecularity (unimolecular,
bimolecular), exergonic endergonic reaction
profile. - Thermodynamics - Reaction spontaneity.
- Organic chemistry.
5Atom - orbitals
SchrÖdinger equation, H?E?
n, ? , m?, Quantum Numbers.
Principle (energy), n 1, 2, 3, , 7, ...
Angular momentum (shape), ? 0(s), 1(p), 2(d),
3(f), ...
Magnetic (orientation), m? - ?, , 0, , ?
Spin, ms ½, -½
6Atomic orbitals - s and p
n1, ? 0, m? 0, ms ½
n2, ? 1, m? 0, ? 1, ms ? ½
7Atomic orbitals - orbital
n2, ? 1, m? 0, 1, or -1, ms ½ or -½
8Atomic orbitals -periodic table
Aufbau Principle
Pauli Exclusion Principle
Hunds Rule
Periodic Table
Textbook
http//www.webelements.com/
9Atomic orbitals - periodic table
10Molecule - covalent bonding
- Lewis Structure, Kekulé structure, octet rule.
- Molecular orbital theory, MOLCAO, bonding
orbital, antibonding orbital. - Hybridization - sp3, sp2, sp, , geometry for
sp3(tetrahedral(Td), 109o), sp2(planar, 120o),
sp(linear, 180o).
11sp3
25 s, 75 p
420 kJ/mol
106 pm
376 kJ/mol
Ethane
12sp2
33 s, 67 p
444 kJ/mol
Ball Spoke
611 kJ/mol
Ethene
Space-Filling
13sp
50 s, 50 p
552kJ/mol
Acetylene
835kJ/mol
14Examples(molecular formula, formal charge,
isomers, hybridization)
- CH4
- NH3
- H2O
- CH3
- CH3-
- H3O
- C2H6
- C2H4
- C2H2
- C2H6O