3.3.11 Amines Flashcards
What is a amine
One or more H+ replaced by an alkyl or aryl group
what are the amines
primary - NH2
secondary - NH
tertiary - N
what is a quarternary amine
an ammonium salt
give a name example of a primary amine
methylamine
ethylamine
Give a name of a secondary amine
dimethylamine
n - methyl propylamine
name a tertiary amine
trimethylamine
benzene and amine
phenyl amine
properties of amines
shape - pyramidal 107 not 109.5 has lone pairs
fishy smell -> tri amines produced when proteins decompose
solubility -> primary up to 4C
not verry soluble water (as hydrogen bonds) and alcohol
Reactivity -> 1. lp used form bonds with H+ - base
2. acts as a nucleophile to bond with a electron deficient carbon
Boiling point of amines
bp - the c is partially positive - n is partially negative
-> polar molecule
primary amine have H+ bonds -> not verry strong -> N electronegative -> short gasses
what kind of base is a amine
Bronsted-Lowry base
accept a H+
alkylamines reactions with acids (eg HCl)
creates an ammonium salt
the ammonium ion and a cl-
woks for phenylamine despite relatively insoluble
What is the inductive effect
alkyl groups release electrons away from the alkyl group towards the N.
inductive effect increases the electronegativity of the N - makes it a better electron pair donor - more reactive
order of the base strengths
ethylamine -> ammonia -> phenylamine
comparing comparing base strengths explained
primary - one inductive effect - better than NH4 because of the inductive effects
secondary - 2 inductive effects = stringer then primary
tertiary - not stronger than 2 as less soluble in H20 <- less H+ bonding
aryl amines -> withdraw electrons from the N <- lp of electron overlap with the delocalization system
n weaker electron pair donor = decrease attractivity to the H+
what is an aliphatic amine
a striaght chain amine