Structure of Organic Compounds Flashcards
Alkane
No functional group: Single bonds between C atoms
Formula: C(n)H(2n+2)
Example: Methane
Alkene
Functional group: At least one double bond between C atoms
Formula: C(n)H(2n)
Example: Prop-2-ene
Alkyne
Functional group: At least one triple bond between C atoms
Formula: C(n)H(2n-2)
Example: Prop-2-yne
Alcohol
Functional group: Hydroxyl (OH-)
Formula: Cn H2n O
Number from end closest to functional group
Suffix: Ol
Example: butan-2-ol
Aldehyde
Functional group: Carbonyl group (C double bond O) on terminal carbon. C double bond is always first carbon in naming
Formula: Cn H2n O
Suffix: al
Example: propanal
Ketone
Functional group: Carbonyl group (C double bond O) on non-terminal carbon
Formula: Cn H2n O
Suffix: one
Example : pentan-3-one
Carboxylic acid
Functional group: Carboxyl group (C double bond O, OH)
Carboxyl is always on carbon 1
Formula: Cn H2n O2
Suffix: oic acid
Example: butanoic aid
Hydrocarbon
An organic compound consisting of only carbon and hydrogen atoms.
Prepositions for naming
Meth, eth, prop, but, pent, hex, hept, oct, non, dec
Haloalkane
Contains at least one halogen (group 17) off a carbon
Number chain so halogen is attached to lowest carbon number
Halogen stem ends in ‘o’ and placed before alkane with location
Example: 2-chloropropane
Branched molecules
Branches are called side chains
End in ‘yl’
Example: 2,3-dimethylbutane
Cyclic molecules
Cyclic hydrocarbon has a ring of hydrocarbons and cyclo as a prefix
Ring is the main chain if it has the most carbons otherwise it is a cycloalkyl group
If there is only one branch or double/triple bond it doesn’t need to be numbered
Number the ring so functional group is number 1
If multiple branches, number carbon to give lowest combination of numbers
Example: 1-ethyl-3-methylcyclopentane
Amines
Functional group: NH2
Suffix: amine
Example: Propan-1-amine
Nitrile
Functional group (C triple bond N)
Nitrile carbon is number 1
Suffix: nitrile
Example: propane nitrile
Esters
Functional group: (C double bond O, single bond O)
Formed by the reaction of a carboxylic acid and an alcohol
suffix: oate