Organic Chemistry Flashcards
(85 cards)
what is the general formula of a compound
(the simplest algebraic formula of a member of a homologous series) e.g. for an alkane: CnH2n+2
what is the structural formula of a compound
(the minimal detail that shows the arrangement of atoms in a molecule) e.g. for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3
what is the displayed formula of a compound
the relative positioning of atoms and the bonds between them
what is the skeletal formula of a compound
the simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups)
*what is a homologous series
(a series of organic compounds having the same functional group but with each successive member differing by CH2)
what is a functional group
(a group of atoms responsible for the characteristic reactions of a compound)
what is an alkyl group
(of formula CnH2n+1)
what does aliphatic mean
(a compound containing carbon and hydrogen joined together in straight chains, branched chains or non-aromatic rings)
what does alicyclic mean
(an aliphatic compound arranged in non-aromatic rings with or without side chains)
what does aromatic mean
(a compound containing a benzene ring)
what is a saturated bond
(single carbon–carbon bonds only)
what is a unsaturated bond
(the presence of multiple carbon–carbon bonds, including C=C, C/C and aromatic rings)
what is a structural isomers
(compounds with the same molecular formula but different structural formulae)
what is homolytic fission *
each bonding atom receiving one electron from the bonded pair, forming two radicals
covalent bond splitting
*(Breaking a covalent bond to form two radical)
what is heterolytic fission*
one bonding atom receiving both electrons from the bonded pair
*(Breaking a covalent bond to form two oppositely charged ions)
what is a radical
a species with an unpaired electron
three stages of homolytic free radical substitution
initiation
propagation x2
termination
what conditions are needed for homolytic free radical substitution
UV light - sunlight
what are problems with homolytic free radical substitution
- reaction is uncontrollable - further substitutions
- radicals can form other organic compounds in the termination stage
- reactions at different positions along the carbon chain
what is a σ-bond:
Overlap of orbitals directly between the bonding atoms
what is a hydrocarbon
compound of hydrogen and carbon only
what is *E/Z isomerism
an example of stereoisomerism, due to restricted rotation about a double bond and two
different groups attached to each carbon atom of the C=C group
what is *Cis–trans isomerism
: A special case of E/Z isomerism in which two of the substituent groups attached to
each carbon atom of the C=C group are the same
what is an electrophile*
An electron pair acceptor