Introduction to organic chemistry Flashcards
hydrocarbon
compound consisting of carbon and hydrogen only
saturated
contains single carbon bonds only
unsaturated
contains a carbon-carbon double bond
molecular formula
the formula which shows the actual number of each type of atom
empirical formula
shows the simplest whole number ratio of atoms of each element in the compound
general formula
algebraic formula for a homologous series
structural formula
shows the minimal detail that shows the arrangement of atoms in a molecule e.g. for butane CH3CH2CH2CH3
displayed formula
shows all the covalent bonds and atoms present in a molecule
skeletal formula
shows the simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups
functional group
a group of atoms / an atom responsible for the characteristic reactions of a compound
homologous series
families of organic compounds with the same functional group and same general formula
characteristics of a homologous series
they show a gradual change in physical properties such as MP as molecular mass increases
Each member differs by CH2 from the last
Same chemical properties
functional group of an alkane
c-c
functional group of alkenes
c(double bond)c
functional group of alcohols
C-OH
Prefix and suffix of alchols
suffix: -ol
prefix : hydroxy-
functional groups of halogenoalkanes
c-halogen
prefix of halogenoalkanes
chloro-
bromo-
iodo-
functional group of aldehydes
on the end of the chain there is a double bond upwards for oxygen and a single bond coming off the carbon for hydrogen
prefix of aldehydes
-al
suffix of aldehydes
formyl-
functional group of ketones
in the middle of the chain there is a double bond upwards coming off a carbon atom for oxygen
suffix of ketones
-one
prefix of ketones
oxo-
functional group of carboxylic acids
at the end of the chain there is a double bond upwards coming off the carbon for oxygen and a single bond coming off the carbon for OH
suffix of carboxylic acids
-oic acids
functional group of esters
in the middle of the chain there is a double bond coming off the carbon for oxygen and also a single bond coming off the carbon for oxygen
order of priority for all homologous series (highest first)
carboxylic acids
Aldehydes
Ketones
Alcohols
Alkenes
Halogenoalkanes
IUPAC rules for nomenclature
- Count the number of carbon atoms in the longest continuous unbranched carbon chain for the stem of the name
- Identify any branches or functional groups
- Number the carbon atoms in the longest chain to indicate positions of branches or functional groups. If there are more than 1 functional groups, put it in alphabetical order
- If the same groups appear more than once, indicate how many times they are present
how do you determine which functional group gets the suffix/prefix
the functional group with the highest priority gets the suffix ending
structural isomers
same molecular formula different structural formula
chain isomers
compounds with the same molecular formula but different structures of the carbon skeleton
position isomers
compounds with the same molecular formula but different structures due to different positions of the same functional group on the same carbon skeleton
functional group isomers
compounds with the same molecular formula but with the atoms arranged to give different functional groups
why is cyclobutane not an alkene even though it follows the general formula of alkenes
it does have the general formula CnH2n but it is not an alkene because it does not contain a carbon-carbon double bond
aliphatic compounds
a compound containing carbon and hydrogen joined together in straight chains, branched chains, or non-aromatic chains
alicylic compounds
an aliphatic compound which contains atoms arranged in non-aromatic rings, with or without side chains
aromatic compounds
a compound containing a benzene ring
formula of benzene
C6H6
steroisomers
same structural formula but different spatial arrangement of atoms
why do E-Z isomers exist
due to the restricted rotation about the carbon-carbon double bond (single carbon-carbon covalent bonds can easily rotate)
There are two different groups/atoms attached to both ends of the double bond
which type of isomerism do alkenes exhibit
E-Z steroisomerism
CIP priority rules
- The atom of higher atomic number which is attached to each side of the double bond, is given priority
- If the atoms are the same, consider the atoms at distance from the double bond. The group containing the atom of higher atomic number is given priority