IUPAC Naming Flashcards
What does naming depend on? (2)
- The chain length (the gives the “parent” name)
- The name and position of functional groups or carbon side chains
rule 1.
Find the longest chain in the molecule and name the molecule
Rule 2.
Establish if there are single, double or triple bonds and add the suffix -ane, -ene or -yne respectively.
Rule 3.
Number the carbons along the longest chain starting from the end closest to a functional group or carbon side chain. To name the carbon side chain use the same system in Rule 1 but add the ending -yl.
Rule 4.
When there is more than one functional group or carbon side chain of the same kind, the figures indicating the positions of the groups are separated by commas reinforced by the use of prefixes ‘di’, ‘tri’ etc.
Rule 5.
Different alkyl groups or functional groups are placed in alphabetical order in the name for a branched hydrocarbon.
Naming and drawing of organic compounds is restricted to __ type of functional group per compound and to maximum of __ functional groups of the same type per compound, except for ____, where a maximum of two different halogen substituents (eg. bromo- and chloro-) are allowed per molecule.
One
Two
Haloalkanes
What are the only substituent chains that are allowed in naming and reactions? (2)
methyl-
ethyl-
A maximum of THREE substituent chains (alkyl substituents) are allowed on ___, ___, ___, ____ or _____ ___ parent chain.
Alkane Alkene Haloalkane Alcohol Carboxylic Acid
When naming haloalkanes, the halogen atoms do not get preference over ___ groups–numbering should start from the end nearest to the first ____, either the alkyl group or the halogen. In haloalkanes where e.g. Br and Cl have the same number when numbered from different ends of a chain, Br gets ____ preference.
Alkyl
Substituent
Alphabetical
Do we ignore di and tri when writing alphabetically?
Yes
Numbers are separated from letters using a…
Numbers are separated from numbers using a….
No spaces except for ___ and ___ ___.
Dash
Comma
Ester
Carboxylic Acid
For euphonic purposes, the vowel “e” is generally removed from the name before the ____. eg. butan-1-ol instead of butane-1-ol. However, this is not done for __. eg. butane-1,2-diol is correct and butan-1,2-diol.
Suffix
Diols
What must be added to the name before the suffix for dienes?
The vowel “a”. eg. buta-1,3-diene is correct, and not but-1,3-diene.
Fluorine
Chlorine
Bromine
Iodine
Fluro-
Chloro-
Bromo-
Iodo-