-
Hydrogenation
- Addition of hydrogen to break
- C=C and triple bonds.
ie: CH3CH=CHCH3 + H2 <=>
-
Saturated
- Alkanes
- A molecule whose carbon atoms bond to the maximum number of Hydrogen atoms.
-
Unsaturated
A molecule that contains a carbon-carbon multiple bond to which more hydrogen atoms can be added.
-
Alkene
A hydrocarbon that contains a carbon-carbon double bond.
-
Alkyne
A hydrocarbon that contains a carbon-carbon triple bond.
-
Cis-Trans isomer
Alkenes that have the same connections between atoms but differ in their three-dimensional structures because of the way that groups attach to different sides of the double bond.
-
Addition reaction
A general reaction type in which a substance X-Y adds to the multiple bond of an unsaturated reactant to yield a saturated product that has only single bonds.
-
Elimination reaction
A general reaction type in which a saturated reactant yields an unsaturated product by losing groups from two adjacent carbons.
-
Substitution reaction
A general reaction type in which an atom or group of atoms in a molecule is replaced by another atom or group of atoms.
-
Rearranged reaction
A general reaction type in which a molecule undergoes bond reorganization to yield an isomer.
-
Hydrogenation
The addition of H2 to a multiple bond to give a saturated product.
-
Halogenation
The addition of Cl2 or Br2 to a multiple bond to give a dihalide product.
-
Hydrohalogenation
The addition of HCl or HBr to a multiple bond to give an alkyl halide product.
-
Hydration
The addition of water to a multiple bond to give an alcohol product.
-
Reaction mechanism
A description of the individual steps by which old bonds are broken and new bonds are formed in a reaction.
-
Polymer
A large molecule formed by the repetitive bonding together of many smaller molecules.
-
Monomer
A small molecule that is used to prepare a polymer.
-
Ethylene
- H2C=CH2
- Polyethylene
- Uses: packaging, bottles
-
Propylene
- H2C=CH-CH3
- Polypropylene
- Uses: bottles, rope, pails, medical tubing
-
Vinyl Chloridey
- H2C=CH-Cl
- Poly(vinyl chloride)
- Uses: Isulation, plastic pipe
-
Styrene
- H2C=CH-(benzene ring)
- Polystyrene
- Uses: Foams and molded plastics
-
Styrene and Buradiene
- H2C=CH-(benzene ring)
- and H2C=CHCH=CH2
- Styrene-butadiene rubber(SBR)
- Uses: synthetic rubber for tires.
-
Acrylonitrile
- H2C=CH-C(triple)N
- Orlon, Acrilan
- Uses: fibers, outdoor carpeting
-
Methyl (methacrylate)
- O
- ||
- H2C=CCOCH3
- |
- CH3
- Plexiglas, lucite
- Uses: Windows, contact lenses, fber optics
-
Tetrafluoroethylene
- F2C=CF2
- Teflon
- Uses: nonstick coatings, bearings, replacement heart valves and blood vessels
-
Aromatic
The class of compounds containing benzene-like rings.
-
Resonance
The phenomenon where the true structure od a molecule is an average among two or more conventional structures.
-
Toluene
A benzene ring with an attached -CH3
-
Phenol
A benzene ring with an attached -OH
-
Aniline
A benzene ring with an attached -NH2
-
Para-Xylene
A benzene ring with two attached -CH3 on oppisite sides of the ring of each other.
-
Benzoic acid
- A bezene ring with a caboxilic acid attached
- O
- ||
- -C-OH
-
Benzaldehyde
- A benzene ring with an attached aldehyde
- O
- ||
- -C-H
-
-
Nitration
The substitution of a nitro group (-NO2) for a hydrogen on an aromatic ring.
-
Halogenation
The substitution oh a halogen group (-X) for a hydrogen on an aromatic ring.
-
Sulfonation
The substitution
-
Cycloalkene
A cyclic hydrocarbon that contains a double bond.
-
Markovnikov's Rule
In the addition of HX to an alkene, the H attaches to the double-bond carbon that has the larger number of H atoms directly attached to it, and the X attaches to the Carbon that has the smaller number of H atoms attached.
|
|