2011年5月26日星期四

Chemical Bonding!

Chemical bonding only involves the valence e-

Formed when e- attracted by nucleus of another


Electrostatic force- opposite charge attract; like charge repel

- greater distance, smaller attraction

- greater charge, greater force.

- the force operates equally in all directions



Intermolecular force=force between molecules

Intramolecular force=force within a molecule


Only weak bonds break in melting process



Chemical bonds exhibit various degrees of sharing, depending on the amount of attraction.



Polarity=molecule's electrical balance, but imbalance with electrical charge of elements



Ionic=electrons are transferred


Non polar covalent=shared equally

- Electronegativity difference <0.5

- Attain full electron shells

- Simultaneously attracted

- high melting points(except CH4, O2, F2)

Polar covalent= shared unequally

- higher energy=partial negative charge=δ-

- lower energy=partial positive charge=δ+

- arrow indicates the migration of electrons

Example

Organic Chemistry May 26, 2011

The chemistry of carbon compounds
.

Importance
-organic compounds are seen anywhere in our life.
-Examples of organic compounds: sugar, chair.......

Properties of organic compounds.
-low melting point
-weak or non-electrolytes
-can forms chains of carbon atoms that are linked in a
①straight-line
 
②circular pattern
③branched pattern
    -can link with other atoms in:
    single bonds
  double bonds
  triple bonds
*Versatility organic compounds makes it such an important branch of chemistry.
Alkanes (unbranched/straight chain)
-A hydrogen : only contains O,H
There are different types of hydrogen
                             ways to present them
-no-polar molecules → immiscible with water
-geometry: tetrahedron
-alkanes are saturated alkanes( all C atoms are bonded by single bonds)
*Saturated: not possible for another atom to bond to the structure.
-Naming of alkanes: the names of all hydrocarbons end in "-ane"
Ex. The structure of C2H6?
          
     full structure                     
②CH3CH2CH3  
Condensed structure
③C3H8
molecular formula

 
Ball-and-Stick model
Names of Alkanes.
methane   CH4
ethane      C2H6
propane   C3H8
butane      C4H10
pentane    C5H12
hexane     C6H14
heptane    C7H16
octane      C8H18
nonane     C9H20
decane     C10H22
They are homologous series: a series of organic compounds with similar general formula, possess similar properties.
CnH(2n+2) -----only for alkanes.
Branched hydrocarbons
hydrocarbons have "side branches" which are also hydrocarbon chains.
(substituted carbon/ branched carbon)
Ex


* Alkyl group: an alkane which has lost one hydrogen atom.
The bottom part are alkyl group(CH3)
 
The name of this branced hydrocarbon is 2-methylpropane
*"-pronpane" is the parent hydrocarbon(longest chain)
Carbon has 4 bonds.
  10 hydrogens
Naming: the names of all alkyl groups end in "-yl", because they are alkyl.
Ex. C2H6      ethyl  C2H5
      C3H8      propyl C3H7

2011年5月11日星期三

Electron Dot & Lewis Diagrams


- nucleus is represented by the atomic symbol
- for individual elements, # of valence electrons
- electrons are represented by dots around the symbol
- a orbit hold a max of 2 electrons
- each orbital gains 1 electron before pair up

Each bond represents 2 electrons
All valence electron must be used
Each element must have a full valence orbital except H


Ex. CH4


Period Table Trend

Metallic Properties:
- the change from metallic to non-metallic going from left to right across the table
- elements become more metallic going down a family


Atomic Radius:
- Decreases across a row from left to right, increase down a group




Reactivity:
- metal&non-metal show different trend
- most metal: Francium
- most non-metal: Fluorine


Ion charge:
- elements ion charges depend on their group


Melting&Boiling point:
- centre of the table-->highest melting/boiling point
- noble gases have lowest melting point


Ionization Energy
- increases up and right
- hellium highest
- Francium lowest


Electronegativity:
- fluorine has highest electronegativity
- Francium has lowest electronegativity