J² + H = Element 119: Kariodisonium
Don't mess with us, we're highly reactive.
Monday, June 6, 2011
Wednesday, June 1, 2011
Functional Groups
-Are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules
-Are generally the most reactive part of the molecule
Halogen Compounds
- contain halogen elements such as F, Cl, Br, I.
- are generally insoluble in water
- compounds containing F are inert, Cl and Br are reactive only under the drastic condition, and I are very reactive
Naming the halogen compounds:Follow the standard rules and put a prefixes of a group attached in front of the main-chain name.
F - fluoro Cl- chloro Br- bromo I - iodo
Nitro Compounds
-Lower nitro alkanes are colorless liquids with a pleasant smell. Higher members are solids
-tend to be explosive (ex. TNT)
Naming the rule: Similar to halogen compounds. Put a prefixes of a group attached in front of the main-chain name. ---- NO2 = nitro
2-Nitropropane
Alcohols
-are organic compounds which contain -OH (hydroxyl) functional group.
- are generally colourless liquids at room temperature
- are soluble in water (smaller alcohols are soluble and larger alcohols are insoluble)
-the hydroxyl group makes the alcohol molecule polar
- are poisonous to some degrees
Naming rule: Follow the standard rules and replace the "E" ending in the parent hydrocarbon chain with the ending "OL".
Aldehydes
- are the organic compounds that contain double bonded oxygen at the end of the chain
-are partially soluble in water
-are very reactive
Naming rule: follow the standard rules and change the parent chain ending to 'AL'Kentones
-are a hydrocarbon chain with a double bonded Oxygen that is not on either end.
-are typically soluble in water
-carbonyl group is polar
Naming rule: follow the standard rules and change the parent chain ending to 'ONE'
Other Functional groups
•Carboxylic Acids
• Esters
• Ethers
• Amides
• Amines
Monday, May 30, 2011
Alkenes & Alkynes
- Are unsaturated, therefore containing double or triple carbon bonds.
- General Formula: CnH2n and CnH2n-2.
- Naming rules similar to Alkanes.
- Endings -ene and -yne are used to name the parent chains in alkenes and alkynes.
Naming Alkenes and Alkynes
- Finds longest continuous chain of carbon atoms. Number the carbons by giving the multiple bond the lowest possible number.
- List and number alkyl groups. Add prefixes if necessary. List them alphabetically.
- Commas used to separate numbers and hyphens are used to separate numbers and letters.
Geometric Isomers
Cis- |
Trans- |
- Labels cis- and trans- are used to distinguish between them.
- Cis- same side
- Trans- across/opposite
Examples:
1-hexene
4-methyl-1-pentene
2,3-dimethyl-1-butene
2,3-dimethyl-2-butene
3-methyl-1-butyne
Thursday, May 26, 2011
Organic Chemistry
Also known as the Chemistry of Carbon compounds
Some properties :
-have low melting points
-weak or non-electrolytes(put in water and break apart)
-can form chains of C2 atoms that linked in a straight line, circular pattern or branched pattern
-can link other atoms in single/double/triple bonds
Alkanes
-are saturated hydrocarbons which are bonded by single bonds
-hydrocarbons = only hydrogen and carbon thus its not possible for another atom to bond to these structures
For naming, hydrocarbons end with '-ane' just cause :)
Carbon= n
2n+ 2=# of H
Hydrocarbons have side branches which are actually hydrocarbon chains.
Akyl groups- removing a hydrogen atom from an orginal alkane
Naming - replace all '-anes' with 'yls'
If there is more than 1 type of alkyl group, put them in alphabetical order with position number in the front, and put a dash in between alkyl group and number.
Some properties :
-have low melting points
-weak or non-electrolytes(put in water and break apart)
-can form chains of C2 atoms that linked in a straight line, circular pattern or branched pattern
-can link other atoms in single/double/triple bonds
Alkanes
-are saturated hydrocarbons which are bonded by single bonds
-hydrocarbons = only hydrogen and carbon thus its not possible for another atom to bond to these structures
For naming, hydrocarbons end with '-ane' just cause :)
Carbon= n
2n+ 2=# of H
Hydrocarbons have side branches which are actually hydrocarbon chains.
Akyl groups- removing a hydrogen atom from an orginal alkane
Naming - replace all '-anes' with 'yls'
If there is more than 1 type of alkyl group, put them in alphabetical order with position number in the front, and put a dash in between alkyl group and number.
Wednesday, May 18, 2011
Chemical Bonding
There are 3 types of Chemical Bonds :
Ionic bonds which rely on the transfer of electrons
Non polar covalent which rely on the sharing of equal amount of electrons
Polar covalent which rely on the sharing of unequal amount of electrons
Electrostatic Force
-is a force that exists between charged particles in ionic compounds as a result of Attraction/ Repulsion
-operates equally in all directions
In ionic bonds, a metal and non-metal bonds together. Metals tend to lose electrons due to its low electronegativity values and non-metals gain electrons since they have high electronegativity values.
Electrongativity is calculated by this method :
ENeg Diff. = lENeg1 - ENeg 2l
Ionic bonds which rely on the transfer of electrons
Non polar covalent which rely on the sharing of equal amount of electrons
Polar covalent which rely on the sharing of unequal amount of electrons
Electrostatic Force
-is a force that exists between charged particles in ionic compounds as a result of Attraction/ Repulsion
-operates equally in all directions
In ionic bonds, a metal and non-metal bonds together. Metals tend to lose electrons due to its low electronegativity values and non-metals gain electrons since they have high electronegativity values.
Electrongativity is calculated by this method :
ENeg Diff. = lENeg1 - ENeg 2l
If ENeg Diff <0.5 it's a non polar covalent bond
If ENeg Diff > 0.5 and <1.8 it's a polar covalent bond
If ENeg Diff > 1.8 it's an ionic bond
In covalent bonds, atoms are held together by intramolecular bonds, they are forces within the molecule and it holds the atoms of the molecule together. These forces are very strong.
However molecules are bonded by intermolecular bonds, which are forces between the molecules itself; they are usually quite weak. In a melting process, only the weak bonds are affected, not the individual molecules.
Polarity
-describes electrical blance of molecule.
-imblance with electrical charge--> polar
-imblance with electrical charge--> polar
-if strength is equal on all sides of molecule--->non polar
Higher electronegativity results in partial negative. (δ- between 0 & -1) Lower electronegativity results in partial positive. (δ+ between 0 & +1) The delta δsymbol represents partial.
Wednesday, May 11, 2011
Electron Dot & Lewis Dot Structures
- Picture representation of the valence electron configuration around an atom.
- Valence electrons represented by dots.
- Nucleus represented by atomic symbol.
- Electrons are placed up to two on each side of the symbol for a maximum of eight, which is a full shell.
- A single electron is placed on each side before pairing them.
- Hydrogen and Helium, only a maximum of 2 electrons (exception).
- Lines between atoms indicate chemical bonds.
- Single lines --> single bonds
- Double lines --> double bonds
- Triple lines --> triple bonds
- Hydrogen and Fluorine never go in center "nucleus"
- Metals are in center
- When one element is singled out, it goes in the center.
Octet Rule
Atoms that combine and form bonds either by transferring electrons to form ions or by sharing electrons in covalent bonds until valence shells are full.
- CNOF (Carbon, Nitrogen, Oxygen and Fluorine) always follow octet rule.
Steps to Drawing a Lewis Structure
1) Pick a Central Atom
- Pick atom with lowest electronegativity
- Central atom: one furthest from obtaining a full shell.
- Connect other atoms with a single bond.
- They might change to double or triple bonds.
2) Count Electrons
- Only worry about the shells in the outer shells.
- Apply Octet Rule: valence shell must contain 8 electrons to be stable.
- Once you know how many electrons to draw around each atom, place them on structure.
- When lone pairs are placed, find atoms that do not fulfill octet rule.
- There may be double or triple bonds formed
- **A pair of electrons form a bond.
- Once electrons are placed, put brackets around the entire structure, if there is a charge on the molecule, write it as a subscript on the upper right, outside the brackets.
Examples:
H2
Cl2
Cl2
H2O
NH₃
O2
NH4+
NH₃
CH₄
O2
N2
NH4+
CO32-
Open circles represent 2 extra electrons from 2- charge.
Wednesday, May 4, 2011
Bohr Model
The Bohr model is the diagram we use today to visualize what an atom looks like.
click to enlarge |
Orbitals: the space occupied by electrons, also known as shells
This is what Bohr believed:
- Electrons have certain energy levels
- When electrons jump to a different orbital, they release a certain spectrum of light
- Ground states are the lowest energy states
- Excited states are when the electrons jump into a higher or lower level
- Each element gives off a certain spectrum of light when they are heated
We use this to identify what elements are present in distant stars
Structure of a Bohr model
Here are the orders of the shells and the maximum electrons they can have
1st shell: 2 electrons
2nd shell: 8 electrons } octet rule
3rd shell: 8 electrons }
In the middle of the diagram, we write the atomic number (number of protons) and the number of neutrons
For example:
The atomic number of chlorine is 17. The atomic mass of chlorine is ~35.
To find the number of neutrons we subtract the atomic number from the atomic mass
35
-17
18
So in the middle of the diagram, we write
17p
18n
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