1unsaturated hydrocarbons that contain one or more carbon-carbon double bonds
alkenes
2general formula of alkenes
CnH2n
3unsaturated hydrocarbons that contain one or more carbon-carbon triple bonds
alkynes
4general formula of alkynes
CnH(2n-2)
5what do you call alkenes with more than one double bond
alkadienes, butadeines, propadeines
6only attractive forces between the molecules of alkenes and alkynes
london dispersion forces
7speeds up (usually Pd) the rate of reaction
catalyst
8addition of H2 to an alkene
hydrogenation
9addition of X2 ( Cl2 / Br2) to an alkene
halogenation
10type of reaction that does not require a catalyst
halogenation
11product of halogenation
dihalide
12product of hydrogenation
alkane
13addition of HX (HCl / HBr) to alkene
hydrohalogenation
14states that the H atom of H-X will bond to the less substituted C atom in the C=C double bond.
Markovnikov's rule
15Addition of water to an alkene
Hydration
16what does hydration require
strong acid, H2SO4
17product formed by hydration
alcohol
18refers to the class of compound that has a six-membered ring with three double bonds
aromatic (benzene ring)
19a hydrocarbon that contains one or more benzene-likek rings
aromatic compound
20a term used to describe aromatic compounds
arene
21who developed the theory of resonance, that provided the first adequate description of the structure of benzene
Linus Pauling
22the substituent group derived by removal of an H from benzene
Phenyl Group (C6H5)
232 substituents: 1,2
ortho- / o
29benzen + COOH
Benzoic Acid
30a hydrocarbon that contains two or more benzene rings, with each pair of rings sharing two adjacent carbon atoms
PAHs Polynuclear Aromatic Hydrocarbon
31Reactions of Benzene
Halogenation, Nitration, Sulfonation
32-OH group bonded to a benzene ring
phenol
33characteristic of phenol
weak acids, insoluble inn water,