1 Introduction to Organic Chemistry Flashcards
(16 cards)
empirical formula
the simplest whole number ratio of atoms of each element in a compound
molecular formula
the true number of atoms of each element in a compound
general fornula
all members of a homologous series follow this e.g. alkanes CnH2n+2
structural formula
shows structural arrangement of atoms within a molecule
displayed formula
shows every atom and every bond in an organic compound
skeletal formula
shows bonds of any non-carbon atoms
homologous series
all follow same general formula and react in similar ways
structural isomerism
same molecular formula, different structures
chain isomerism
same molecular formula, different carbon chain
e.g. C4H10 CH3CH2CH2CH3 or CH3CH(CH3)2
what happens as branching increases?
boiling point decreases as molecule chains can pack less tightly so aren’t as close together
functional group isomerism
same molecular, different functional group
alkenes and cycloalkanes
alcohols and ethers
aldehydes and ketones
position isomerism
same molecular formula but functional group is in a different position along the chain
stereoisomerism
same molecular formula and structural formula but bonds arranged differently in space
why does geometric isomerism occur?
both sides of the C=C bond have different groups attached and there is no rotation around the C=C
E-Z isomers
E Isomers: on OPPOSITE sides of the bond
Z isomers: on the SAME side of the bond
CIP priority rules
The first atom bonded to the carbon which has the HIGHER Ar is given higher priority
e.g. if Br and C bonded to a C=C, Br is given priority
if the same Ar, look to atom bonded to that one