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1. amine: derivative of ammonia where one or more hydrogen replaced by carbon-based groups
2. primary amine: R-NH2
3. secondary amine: R2NH
4. tertiary amine: R3N
5. Ammonia: NH3
6. quarternary amine: a configuration in which nitrogen has four bonds with other atoms and, as such, the
molecule has an electron deficit
7. name by alkyl group +amine at the end: naming simple amines
8. Ethylamine:
9. diethylamine:
10. triethylamine:
11. cyclohexylamine:
12. name parent chain and then name amine as amino substituent: naming amines
with additional functional groups present
13. 3-aminobutanoic acid:
14. 2,4-diaminobenzoic acid:
15. 1,4-diaminobutane:
16. 4-amino-2-butanone:
17. name amine as N-substituted where largest compound = parent
name other groups as N-alkyl substituents: naming unsymmetrically substituted 2nd and 3rd
degree amines
18. N-ethyl-N-methylpropylamine:
19. N,N-dimethylpropylamine:
20. N-ethyl-N-methyl-cyclohexylamine:
21. amino groups direct attached to aromatic ring: aryl amine naming
22. aninline/ aminobenzene:
23. benzylamine:
24. trigonal pyramidal, 109.5 bond angle: amine geometry
25. polar: amine polar or nonpolar?
26. primary and secondary amines can form intermolecular hydrogen bonds-
: amine hydrogen bonding?
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, chem 219 Organic Chemistry Module 6 Exam Portage updated questions
with 100% correct answers | updated and verified 2024
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27. higher than alkanes
lower than alcohols: boiling points of 1st and 2nd degree amines?
28. N-H bond weaker than O-H bonds bc N is less electronegative than O: why
are amines lower bp than alcohols?
29. can accept hydrogen bonds but cannot make them intermolecularly: can
tertiary amines have hydrogen bonds?
30. small amines (up to 6 carbons) are soluble: are amines soluble in water? in alcohol?
31. solubility decreases as molecular weight increases: amine aqueous solubility does
what?
32. basic and nucleophilic: are amines acidic or basic?
33. pKb (lower score = more basic): what measures bases
34. alkyl: 3-4, aromatic: 9 (resonance sharing in aromatic): pKb of alkyl amines vs aromatic
amines
35. amine: ammonia + alkyl halide =
36. 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: 2 steps to alkylation of ammonia and amines
37. alkyl halide added to an ammonia to create an amine: alkylation of ammonia and
amines
38. secondary amine (R2NH): what does a primary amine alkylate to?
39. tertiary amine (R3N): What does a secondary amine alkylate to?
40. quaternary ammonium salt: what does a tertiary amine alkylate to?
41. can produce all degrees of amines: what is advantage of alkylation of amines ?
42. Polyalkylation: yield a mix of amine products because no reaction stops
cleanly after a single alkylation: what is the disadvantage of alkylation of amines?
43. use large concentration of ammonia or amines as the excess helps the
halides not react with the new amines created: how to combat possible polyalkylation?
44. reduced state: all bonds to Nitrogen are either Carbons or Hydrogens
45. Catalytic Hydrogenation: reducing an aromatic nitrogen compound to an aromatic primary amine
on a metal catalyst like nickel or platimum with the addition of high pressured hydrogen gas
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