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Alkene
has a double bond between two carbons, name ends in ene
Alkyne
has a triple bond between two carbons, name ends in yne
Arene
aromatic ring, has no name ending
Halide
Carbon is bonded to F, CL, Br or I
Alcohol
Carbon is bonded to an OH group, ends in ol
Ether
there is an oxygen bonded to two carbons, name ends in ether
sulfide
sulfur bonded between two carbons, ends in sulfide
disulfide
c-s-s-c, ends in disulfide
methane
CH4
Ethane
C2H6
Propane
C3H8
Butane
C4H10
Pentane
C5H12
Hexane (5 isomers)
C6H14
Heptane (9 isomers)
C7H16
Octane (18 isomers)
C8H18
Nonane (35 isomers)
C9H20
Decane (75 isomers)
C10H22
Undecane
C11H24
Dodecane
C12H26
Tridecane
C13H28
Icosane
C20H42
Triacontane
C30H62
constitutional isomer
a compound that has the same molecular formula, but the atoms are connected differently
Alkyl group
what is left over when a hydrogen atom is removed from an alkane, replace the ane ending with the yl ending
functional group
a group of atoms within a molecule that have a characteristic chemical behavior
Organic acids
methanol (CH3OH), acetic acid (CH3CO2H) , acetone (CH3COCH3)
Carboxylic acids
contain the -CO2H grouping
organic bases
characterized by the presence of an atom with a lone pair of electrons that can bond to H+
Lewis acid
a substance that accepts an electron pair
Lewis base
a substance that donates and electron pair
Bronsted-Lowry acid
a substance that donates H+
Bronsted-Lowry base
substance that accepts H+
pKA and acid relationship
the higher the pKa value, the more basic a substance is
predicting Acid-base reaction
H+ will always go from the stronger acid to the stronger base
resonance structures
bonds can change but location of molecules will not