13. Intro To Organic Flashcards
hydrocarbon
a compound made up of C and H atoms only
alkanes
simple hydrocarbons with no functional group
functional group
dictates physical and chemical properties of compounds.
homologous series- functional group
alkene- c-c double bond
halogenoalkane- halogen R-X
alcohol- hydroxyl R-OH
aldehyde- carbonyl R-CHO
ketone- carbonyl R-CO-R
carboxylic acid- carboxyl R-COOH
ester- R-COO-R
amine- R-NH2
nitrile- R-CN triple bond
(a) homologous series
(b) saturated and unsaturated
(c) homolytic and heterolytic fission
(a) homologous series-
(b) saturated-
unsaturated-
(c) homolytic-
heterolytic fission-
(d) free radical, initiation, propagation, termination
(e) nucleophile, electrophile, nucleophilic, electrophilic
(f) addition, substitution, elimination, hydrolysis, condensation
(g) oxidation and reduction
oxidation- loss of electron and hydrogen, gain of oxygen and oxidation no.
reduction- gain of electron and hydrogen, loss of oxygen and oxidation no.
symbol [O] represent one atom of oxygen from an oxidising agent.
symbol [H] represent one atom of hydrogen from a reducing agent.
(a) free-radical substitution
(b) electrophilic addition
(c) nucleophilic substitution
(d) nucleophilic addition
use of curly arrows to represent movement of electron pairs; the arrow should begin at a bond or a lone pair of electrons.
FRS- alkanes
EA- alkene to
NS- alcohol to halogeno and reverse
NA-
organic molecules are
shape of, and bond angles in, molecules containing sp, sp2 and sp3 hybridised atoms
arrangement of σ and π bonds in molecules containing sp, sp2 and sp3 hybridised atoms
straight-chained, branched or cyclic
planar when describing the arrangement of atoms in organic molecules, for example ethene
structural isomerism
chain-
positional-
functional group-
stereoisomerism
geometrical (cis/trans)-
optical isomerism (use of E/Z)-
geometrical (cis/trans) isomerism in alkenes
what is meant by a chiral centre
such a centre gives rise to two optical isomers (enantiomers). comounds can contain more than one chiral centre.