CHEM 219 Module 6 Problem Set Principles of Organic
Chemistry with Lab FINAL EXAM STUDY GUIDE
2025/2026 COMPLETE QUESTIONS WITH CORRECT
DETAILED ANSWERS || 100% GUARANTEED PASS
<BRAND NEW VERSION>
2 steps to alkylation of ammonia and amines .....Answer.....1.
ammonia as nucleophile displaces halide ion via Sn2 reaction
2.sodium hydroxide (base) added to deprotonate the
alkylammonium cation to produce the "free base" of the amine
what is the disadvantage of alkylation of amines?
.....Answer.....Polyalkylation: yield a mix of amine products
because no reaction stops cleanly after a single alkylation
,age 2 of 46
how to combat possible polyalkylation? .....Answer.....use large
concentration of ammonia or amines as the excess helps the
halides not react with the new amines created
amine aqueous solubility does what? .....Answer.....solubility
decreases as molecular weight increases
alkylation of ammonia and amines .....Answer.....alkyl halide
added to an ammonia to create an amine
what does a primary amine alkylate to? .....Answer.....secondary
amine (R2NH)
What does a secondary amine alkylate to? .....Answer.....tertiary
amine (R3N)
what does a tertiary amine alkylate to? .....Answer.....quaternary
ammonium salt
,age 3 of 46
what is advantage of alkylation of amines ? .....Answer.....can
produce all degrees of amines
derivative of ammonia where one or more hydrogen replaced
by carbon-based groups .....Answer.....amine
R-NH2 .....Answer.....primary amine
R2NH .....Answer.....secondary amine
R3N .....Answer.....tertiary amine
NH3 .....Answer.....Ammonia
a configuration in which nitrogen has four bonds with other
atoms and, as such, the molecule has an electron deficit
.....Answer.....quarternary amine
, age 4 of 46
naming simple amines .....Answer.....name by alkyl group +amine
at the end
.....Answer.....Ethylamine
.....Answer.....diethylamine
.....Answer.....triethylamine
.....Answer.....cyclohexylamine
naming amines with additional functional groups present
.....Answer.....name parent chain and then name amine as amino
substituent
.....Answer.....3-aminobutanoic acid
.....Answer.....2,4-diaminobenzoic acid
.....Answer.....N-ethyl-N-methylpropylamine