Nomenclature Flashcards
nomenclature of alkanes
- id longest chain
- use number prefix
- use “-ane” suffix
- id substituents
- number carbons
- substituents on lowest numbers possible
- group identical substituents together w/prefixes
- alphabetized substituents (ignore prefixes)
example = 4-isopropyl-2,3,3-trimethylheptane
(P 38-41)
nomenclature of haloalkanes
- follow the same rule as simple alkanes
- use halogen prefixes
- F = fluoro-
- Cl = chloro-
- Br = bromo-
- I = iodo-
(P 41-42)
nomenclature of alcohols
- denote hydroxyl group with suffix to main alkyl chain (replace “e” with “-ol”)
- place number of hydroxyl group after name of the longest C chain, before “-ol” suffix
- give hydroxyl group the lowest number possible
example = 3-methylbutan-2-ol
(P 43-44)
1 carbon chain
- prefix = meth-
(P 32)
2 carbon chain
- prefix = eth-
(P 32)
3 carbon chain
- prefix = prop-
(P 32)
4 carbon chain
- prefix = but-
(P 32)
5 carbon chain
- prefix = pent-
(P 32)
6 carbon chain
- prefix = hex-
(P 32)
7 carbon chain
- prefix = hept-
(P 32)
8 carbon chain
- prefix = oct-
(P 32)
9 carbon chain
- prefix = non-
(P 32)
10 carbon chain
- prefix = dec-
(P 32)
methyl substituent
- -CH3
(P 33)
ethyl substituent
- -CH2CH3
(P 33)
propyl substituent
- -CH2CH2CH3
(P 33)
isopropyl substituent
(P 33)

sec-butyl substituent
(P 33)

tert-butyl
(P 33)

alkane functional group
- R3C-CR3
(P 34)
alkene functional group
- R2C=CR2
(P 34)
alkyne functional group
- RC ≡ CR
(P 34)
alkyl halide functional group
- R-X
(P 34)
alcohol functional group
- R-OH
(P 34)
thiol functional group
- R-SH
(P 34)
ether functional group
- R - O - R
(P 34)
epoxide functional group
(P 34)

phenol functional group