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Neutrons
no charge, in nucleus
Protons
Positive charge, in nucleus
Electrons
Negative charge, outside nucleus
Alkali Metals
-Group one
-soft and silvery
-melt at low temp
-produce H2 with water
-single electron
Alkaline Earth Metals
-Group 2
-soft
-in nature as oxides
-2 electrons
Halogens
-Group 17
-very reactive
-F and C are gases
-Br and I are solids
Noble Gases
-Group 18
-colorless, odorless gas
-full outer shell
-unreactive
-low temp crygenics
-absorb and emit electromagnetic radiation
Transition Metals
-Groups 3-12
-Highly colored compound
Lanthanides and Actinides
-Heavy metals
-can form compound in several oxidation states
-actinides are radioactive in nature
Atomic Radii
Size of the atom
Increase left and down table
Ionic Radius
Distance between nucleus and outermost ion
Increase left and down table
Electronegativity
Tendency for an atom to attract electrons toward itself
Increase right and up table
Ionization Energy
Minimum energy to lose outer most ion
Increase right and up table
Octet Rule
-Elements try to attain number of electrons as closest noble gas
-Want to have 8 in outer shell
-Will gain or lose electrons
Electron Configuration
Distance of electrons within the levels
-conttrols chem and physical properties
-N
-I
-M1
-M2
-Principle Energy
-subshell
-orbital
-spin
How many electrons and sub shells?
-n=1
-n=2
-n=8
-holds 8 electrons, two subshells
-holds 18 electrons, three sub shells
How many orbitals and shape?
-s
-p
-d
-f
-3 orbitals, dumbbell
-5 orbitals, clover
-7 orbitals
Hund's Rule
orbitals of equal energy are each occupied by one electron before any orbital is occupied by a second electron, and all electrons in singly occupied orbitals must have the same spin
Ionic Bond
attraction of oppositely charged ions
large difference in electronegativity
Covalent Bond
sharing electrons of uncharged atoms
small difference in electronegativity
Lewis Structure
Diagram of an element showing its valence electrons as dots
Discrete Ions
Hydroxide, Carbonate, Bicarbonate, Sulfate, Sulfite, Nitrate, Nitrite
VSEPR
Valence shell electron pair repulsion theory
Lone Pairs
Treated like bonding pairs and repelled by valence electrons; slightly more repulsive
Order or repulsion
Lone pair-lone pair > lone pair-bond pair > bond pair-bond pair
What direction is the atom?
-line
-dashed
-filled
-in the plane of the paper
-backward into the page
-forward from the page
Mole
the amount of a substance that contains as many units there atoms in an element
Avogadro's number
6.022 x 10^23
State symbols
-s
-l
-g
-aq
-solid
-liquid
-gas
-aqueous
Solubility of ionic substances
-solubility in water varies
-depends on relative attraction of ions for each other and for water molecules
Solubility of non ionic substances
-water dissolves non-ionic substances
-polar substances are only soluble in polar solutions
Concentration
A measurement of how much solute exists within a certain volume of solvent
Molarity (M) = mol/L
Theoretical and Percentage Yields
-amt of product when limiting reagent is completely consumed
-actual yield of a product in % of theoretical (actual/theoretical x 100)
Electrolyte
-strong
-weak
-non
a substance that dissolves to give a solution that contains ion
-mainly ions
-mainly molecules
-doesn't conduct
Oxidation Rules
1. oxidation # of an ion equal the charge on that ion
2 oxidation # of an uncharged element is 0
3. an increase in oxidation # indicates oxidation
4. a decrease in oxidation # indicates reduction
5. -oxidation # of H = -1 in compounds with metals, +1 in compounds with nonmetals
-oxidation # of O = always -2, except peroxide = -1
-oxidation # of F = always -1
-oxidation # of all other halogens = -1 except if bound to oxygen or halogen w/ large atomic weight
6. oxidation # of a compound w/ several atoms is = sum of oxidation # of all atoms
Half Reactions
split reactions into reduction and oxidation to see electron transfer
step 1: reduce ions
step 2: balance half equation; add electrons, water, or H ions
step 3: combine half equations
Isotopes
atoms with the same number of protons but different number of neutrons
Radioactive Decay
1. alpha
2. beta
3. y-emission
4. position emission
5. electron capture
unstable nucleus emits radiation, forms another nucleus
1. helium nucleus ejected
2. neutron converted to proton
3. nucleons reorganize into more stable arrangement, high energy photons released
4. unstable nuclides which are neutron deficient, proton -> neutron + high energy position
5. nucleus captures electron from electron cloud
Radioactive Half-life
Time to reach half of initial value
Carbon Properties
1. can form 4 strong, stable bonds to a lot of elements
2. can form stable double bonds and triple bonds
3. suitable electronegativity for polar bonds
4. abundant
Hybridization
mixing of atomic orbitals to produce equivalent # of hybrid orbitals - energetically favorable
Sigma Bond
single bond between 2 atoms
Hydrocarbon
most simple organic molecule, contains C & H, acyclic or cyclic
Alkanes
Saturated hydrocarbons with one covalent bond between carbon atoms and each have sp3 hybrid orbitals - CnH2(n+2)
Alkenes
unsaturated hydrocarbons with greater than or = 1 double or triple bonds between carbon atoms - CnH2n
Pi-bond
contains electrons for chem reeactios - weaker and broken to two sigma bonds
Naming
1. Parent
2. Suffix
3. Prefix
4. Locants
1. describes main carbon section
2. identifies the principle functional group
3. identifies the substituents on the main chain or ring
4. shows where the substituents are located
Naming Rules
1. identify longest carbon chain containing the most functional groups
2. identify the most important functional group and add suffix
3. name and substituents, if >1 add number (di, triple, tetra)
4. specify substituents location, hyphen to separate # and letters, commas to operate # and #
Nucleophiles
Nucleus loving, electron rich reagent that forms a bond by donating an electron pair -becomes a neg charged anion
Electrophiles
Electron loving, electron deficient reagent that forms a bond by accepting an electron pair - becomes pos charged cation
Organic Reaction Mechanism
Step-by-step account of how a reaction of organic compounds take place
- use curly arrow
1. creating bonds
2. shared pair moves to adjacent binding location
3. breaking bonds