Chapter Twenty Three Topic Classificatio PDF

Chapter Twenty Three
Topic: Classification of amines

Section: 23.1
Difficulty Level: Easy
1. Which of the following is a primary amine?

A) CH3CH2CH2CH2NH2
B) CH3CH2NHCH2CH(CH3)2
C) (CH3CH2)2NCH2CH(CH3)2
D) (CH3CH2)4N+ OH-
E) (CH3CH2)3N
Ans: A

Section: 23.2
2. Which of the following is a secondary amine?

A) CH3CH2CH2CH2NH2
D) (CH3CH2)4N+ OH-
E) (CH3CH2)3CNH2
Ans: B

Section: 23.1
3. Which of the following is a tertiary amine?

A) CH3CH2CH2CH2NH2
D) (CH3CH2)4N+ OH-
E) (CH3CH2)3CNH2
Ans: C

Section: 23.1
4. Which of the following is a quaternary ammonium salt?
A) CH3CH2CH2CH2NH3+ Cl-
B) (CH3CH2)2NH2+ Cl-
C) (CH3CH2)3NH+ Cl-
D) (CH3CH2)4N+ Cl-
E) none of these
Ans: D

Section: 23.1
Difficulty Level: Medium
5. Classify the following compounds as a primary, secondary or tertiary amine.

H
NH2
N
N O
I II III
Ans: I-secondary amine
II-tertiary amine
III-primary amine
Topic: Nomenclature of amines

Section: 23.2
6. What is the structure for 1-butanamine?

A) CH3CH2CH2CH2NH2
D) (CH3CH2)4N+ OH-
E) (CH3CH2)3CNH2
Ans: A

Section: 23.2
7. What is the common name for the following compound?
A) ethylethylisobutylamine
B) diethylisobutylamine
C) sec-butyldiethylamine
D) 2-diethylaminobutane
E) none of these
Ans: C

Section: 23.2
A) ethylisobutylisopropylamine
B) ethylisopropylbutylamine
C) sec-butylethylpropylamine
D) sec-butylethylisopropylamine
E) none of these
Ans: A

Section: 23.2

H
N
A) dibenzylamine
B) diphenylamine
C) dibenzeneamine
D) phenylbenzeneamine
E) none of these
Ans: B

Section: 23.2
10. What is the IUPAC name for the following compound?
H
N
A) N-ethylhexanamine
B) N-ethylcyclohexanamine
C) N-cyclohexylethanamine
D) N-ethylcyclopentanamine
E) N-ethylaniline
Ans: B

Section: 23.2
A) N-cyclopentyl-N-methylcyclohexanamine
B) N-cyclohexyl-N-methylcyclohexanamine
C) N-cyclopentyl-N-methylcyclopentanamine
D) cyclohexylcyclopentylmethylamine
E) N-pentyl-N-methylhexanamine
Ans: A

Section: 23.2
H
N
A) 1-methyl-N-propyl-1-butananmine
B) 4-methyl-5-octanamine
C) 1-ethyl-N-propyl-1-pentanamine
D) N-butyl-2-pentanamine
E) N-methylpropyl-1-butanamine
Ans: D

Section: 23.2

NH2
Ans: 5-cyclopropyl-1-heptanamine

Section: 23.2
NH2
Ans: (1S,2S)-2-methyl-1-cyclopentanamine

Section: 23.2
15. What is the structure for 3-chloro-N-ethylpentanamine?

Ans: H
N
Cl

Section: 23.2
16. What is the structure for N-ethylbenzylamine?

Ans:
N
H

Section: 23.2
17. What is the structure for N,N-diethylaniline?

Ans:

Section: 23.2
Difficulty Level: Hard
OH NH2
Ans: 7-amino-5-isopropyl-3-octanol

Section: 23.2
NH2
HO
O
Ans: 4-amino-2,2-diethylhexanoic acid
Section: 23.2

HO
O NH2
Ans: 7-amino-5-ethyl-1-hydroxy-3-octanone

Section: 23.2

O
NH2
Ans: 3-amino-4-ethylcyclohexanone

Section: 23.2

NH2
Ans: (1R,6R)-6-methylcyclohex-2-enamine
Topic: Properties of amines

Section: 23.3
23. Arrange the following compounds in decreasing (highest to lowest) order of boiling
point.
CH3CH2CH2CH2NH2 CH3CH2N(CH3)2 CH3CH2CH2NHCH3
I II III
A) II>III>I
B) I>III>II
C) II>III>I
D) III>II>I
E) I>II>III
Ans: B

Section: 23.3
24. Arrange the following compounds in decreasing (highest to lowest) order of boiling
point.
1-pentanol hexane 1-pentanamine butyl methyl ether
I II III IV
A) III>I>IV>II
B) I>III>IV>II
C) I>IV>III>II
D) I>III>II>IV
E) III>I>II>IV
Ans: B

Section: 23.3
25. Which of the following compounds is most soluble in water?

NH2
N N
H
II III
I
A) I
B) II
C) III
D) both I & II
E) all of these
Ans: B

Section: 23.3
26. Which of the following compounds is least soluble in water?
NH2
N N
H
II III
I
A) I
B) II
C) III
D) both I & III
E) none of these
Ans: C

Section: 23.3
27. Arrange the following amines in decreasing (most to least) order of solubility in water.
NH2
N N
H
II III
I
A) III>I>II
B) I>III>II
C) I>II>III
D) II>I>III
E) III>II>I
Ans: D

Section: 23.3
28. Which of the following compounds is the strongest base?

NH2 NH2 NH2 NH2
NH2
Cl
O2N IV V
I II III
A) I
B) II
C) III
D) IV
E) V
Ans: D

Section: 23.3
29. Rank the following compounds in decreasing (strongest to weakest) order of basicity.
NH2 NH2 NH2
NH2
O2N
II III IV
I
A) I>III>II>IV
B) II>III>I>IV
C) IV>II>III>IV
D) IV>III>II>I
E) III>II>I>IV
Ans: D

Section: 23.3
30. Arrange the following compounds in decreasing (strongest to weakest) order of basicity.
CH3CH2NH2 (CH3CH2)3N NH3 (CH3CH2)2NH
I II III IV
A) I>III>II>IV
B) II>III>I>IV
C) IV>II>I>III
D) IV>III>II>I
E) II>I>IV>III
Ans: C

Section: 23.3
p-toluidine aniline p-nitroaniline p-methoxyaniline
I II III IV
A) I>III>II>IV
B) II>III>I>IV
C) IV>III>II>I
D) IV>I>II>III
E) II>I>IV>III
Ans: D

Section: 23.3
O NH2
NH2 NH2 NH2
CF3 OCH3
IV
II III
I
A) I>III>II>IV
B) II>III>I>IV
C) IV>III>II>I
D) IV>I>II>III
E) II>IV>I>III
Ans: E

Section: 23.3
33. Arrange the following compounds in increasing (weakest to strongest) order of basicity.
NH2
H
N
NH2
NO2
I II III IV
A) IV<II<I<III
B) III<II<IV<I
C) II<I<III<IV
D) II<III<I<IV
E) None of
Ans: C

Section: 23.3
34. Which one of the following is a stronger base? Explain why.
NH
N
I II H
Ans: I is a stronger base.
The nitrogen is connected to sp3C and the non bonding electrons on nitrogen are
not involved in resonance with the aromatic ring, whereas the nitrogen in II is
connected to sp2C and the non bonding electrons on nitrogen are delocalized over
the aromatic ring.

Section: 23.3
35. Pyridoxamine, aka vitamin B6 has the following structure. Which nitrogen is more
basic? Explain your choice.
1
CH2NH2
HO CH2OH
H3C N
2
Ans: N1 is more basic as it is sp3 hybridized and is less electronegative because of less
s character, than the sp2 hybridized N2. The non bonding electrons are more easily
available in N1 than N2.

Section: 23.3
36. Nicotine present in tobacco has the following structure. Which nitrogen is more basic
and explain your choice.
N
2
CH3
N
1
Ans: N2 is more basic as it is sp3 hybridized and less electronegative because of less s
character.

Section: 23.3
37. Chloroquine is used as an antimalarial drug. Rank the three nitrogen atoms in decreasing
(strongest to weakest) order of basicity.
III
I
N
HN
Cl N
II
A) III>I>II
B) I>III>II
C) I>IV>III>II
D) I>III>II>IV
E) III>II>I
Ans: E
Topic: Preparation of amines

Section: 23.4
Difficulty: Easy
38. Predict the product for the following reaction.
CN H2/Ni
NH2
NH2 CN
I II III
O
NH2 NH
IV V
A) I
B) II
C) III
D) IV
E) V
Ans: B

Section: 23.4
Difficulty: Medium

Br
1. NaCN
2. LiAlH4
3. H2O
CN NH2 NH2
NH2
III O
I II
IV
A) I
B) II
C) III
D) IV
E) none of these
Ans: C

Section: 23.4
40. Provide the reagent(s) necessary to carry out the following conversion.
NO2 NH2
A) H2/Ni
B) 1. LiAlH4 2. H2O
C) Fe/HCl
D) NaBH4/CH3OH
E) all of these
Ans: C

Section: 23.4

O
NH2 1. LiAlH4
2. H2O
OH
NH2
NH2 NH2
I II III
H2N
H2N
O
OH
V
IV
A) I
B) II
C) III
D) IV
E) V
Ans A

Section: 23.4
O
NH 1. LiAlH4
2. H2O
OH
O
NH NH
H2 N H2N
NH2
O
OH
I II III IV V
A) I
B) II
C) III
D) IV
E) V
Ans A

Section: 23.4
43. Provide the reagents necessary to carry out the following conversion for the following
reaction.
O
N N
Ans 1. LiAlH4
2. H2O

Section: 23.4
44. Predict the product for the following reaction sequence.
OH SOCl2 CH3NH2 1. LiAlH4

pyridine 2. H2O
O
Ans: H
N

Section: 23.4
45. Provide the reagents necessary to convert (S)-3-methyl-3-phenylpentanoic acid to

(S)-3-methyl-3-phenylpentanamine.
Ans: 1. SOCl2/pyridine
2. NH3
3. LiAlH4
4. H2O

Section: 23.4
46. Provide the reagents necessary to carry out the following conversion.
CH2Br CH2CH2NH2
Ans: 1. NaCN
2. LiAlH4
3. H2O

Section: 23.5
CH2CN CH2CH2NH2
Ans: 1. LiAlH4
2. H2O

Section: 23.5

Br 1. NaN3
2. LiAlH4
3. H2O
NHNH2 NH2 NNH2

N
NH
I II III IV
A) I
B) II
C) III
D) IV
E) III & IV
Ans: B

Section: 23.5

Br
1. NaN3
2. LiAlH4
3. H2O
Ans: NH2
Section: 23.5
50. Predict the product for the following reaction and provide a stepwise curved arrow
mechanism for the formation of the product.
1. LiAlH4
N3
2. H2O
Ans:
NH2
Mechanism
H
H
N AlH3
N
N N
N
N O
N
H H
H
+ N N
H Al H
H
NH2 + OH

Section: 23.5

mCPBA NaN3 1. LiAlH4
2. H2O
OH N3 NH2 OH OH
NH2 OH OH NH2 N3
+ enantiomer + enantiomer + enantiomer + enantiomer + enantiomer
I II III IV V
A) I
B) II
C) III
D) IV
E) V
Ans: A

Section: 23.5
52. Which of these alkyl halides cannot be used to prepare amines using Gabriel synthesis?
A) 1-bromopentane
B) 1-bromo-3-methylbutane
C) 2-bromo-3-methylpentane
D) 1-bromo-2,3-dimethylbutane
E) 2-bromo-2,3-dimethylbutane
Ans: E

Section: 23.5
53. Predict the product(s) for the following reaction.

O
1. KOH
NH
2. CH3CH2CH2CH2Br
+
3. H3O
O
O O
COH CNH2
NH2
+ NH2 +
COH COH
I II
O O
O O
CNH2
+ NH2 N
COH
III IV
O
O
A) I
B) II
C) III
D) IV
E) None of these
Ans: A

Section: 23.5
54. Provide a stepwise synthesis of 3-amino-2-methylpentane using the Gabriel synthesis.

O
Ans: O O
KOH Br N
NH NK
O O O
O
COH
H3O+
+
NH2
COH

Section: 23.5
55. Provide a stepwise synthesis of 1-cyclopentylethanamine using the Gabriel synthesis.

Ans: O O Br O
KOH N
NH NK
O O O
O
NH2 COH
H3O+
+
COH

Section: 23.5
O
+
KOH Br H3O
NH
O
Ans:
NH2

Section: 23.6

O
NH2
H2SO4, NaBH3CN
NCH2CH3 NHCH2CH3
HO
NHCH2CH3
II III
I
O
H3CH2CHN
NHCH2CH3
N
IV V H
A) I
B) II
C) III
D) IV
E) V
Ans: B

Section: 23.6
NH2
O
H2SO4, NaBH3CN
N O HN
HO NH
III IV
I II
A) I
B) II
C) III
D) IV
E) None of these
Ans: D

Section: 23.6
H
N
Ans: O
1. CH3CCl / AlCl3
2. CH3CH2NH2, H2SO4, NaBH3CN

Section: 23.6
60. Provide the structures of the products in the following reaction sequence.
1. BH3 PCC (CH3)2NH

A B C
2. H2O2, NaOH/H2O H2SO4, NaBH3CN
Ans: B C
A
N(CH3)2
OH O N(CH3)2
+ enantiomer + enantiomer
N(CH3)2 N(CH3)2

Section: 23.6
61. Provide the structures of the products in the following reaction sequence.
H
N
H3O+ PCC
A B C
H2SO4, NaBH3CN
Ans:
OH O N
A B C

Section: 23.6
CN
O N
Ans: 1. HOCH2CH2OH/TsOH
2. H2/Pt
3. H3O+

Section: 23.6
Cl
(CH3)2NH
AlCl3 H2SO4, NaBH3CN
N
N O
N
O
OH
II
I III
IV
A) I
B) II
C) III
D) IV
E) none of these
Ans: D
Topic: Reactions of amines

Section: 23.8
Cl
Cl
NHCCH 2CH3
O
Ans: 1. Cl2/FeCl3
2. HNO3/H2SO4
3. Cl2/FeCl3
4. Fe/HCl
O
5. CH3CH2CCl

Section: 23.8
NO2 NH2
Br
Ans: 1. Fe/HCl
O
2. CH3CCl
3. Br2/FeBr3
4. H3O+
5. dil. Na2CO3

Section: 23.9
66. Predict the major product for the following reaction.
NH2
1. excess CH3I
2. Ag2O, H2O
heat
N(CH3)2 OH
I II III IV
A) I
B) II
C) III
D) IV
E) I & III
Ans: B

Section: 23.9

1. excess CH3I
NH2
2. Ag2O, H2O
heat
I II III
IV
A) I
B) II
C) III
D) IV
E) I & III
Ans: A

Section: 23.9
1. excess CH3I
2. Ag2O, H2O
N heat
N N
N N
IV V
II III
I
A) I
B) II
C) III
D) IV
E) V
Ans: E

Section: 23.9

1. excess CH3I
2. Ag2O, H2O
N heat
Ans:

Section: 23.9
1. excess CH3I
NH2
2. Ag2O, H2O
heat
Ans:

Section: 23.9
O
NH2
O
A B C
HO
NH2
Ans: A. 1. NH3, 2. H2/Pt

B. 1. excess CH3I, 2. Ag2O, H2O
C. mCPBA
D. NH3

Section: 20.10 & 20.11
NO2 NO2
NH2 Cl
Ans: 1. NaNO2/HCl; < 50C
2. CuCl

Section: 20.10 & 20.11
73. Provide the reagent A, necessary to carry out the following conversion.
Br Br
NH2 OCH3
NaNO2/HCl A
0
<5 C
Br Br
A) H3PO2
B) HCN
C) H2O
D) CH3OH, heat
E) NaOCH3
Ans: D

Section: 20.10 & 20.11
74. Provide the reagent A, necessary to carry out the following conversion.
Br Br
NH2
NaNO2/HCl A
0
<5 C
Cl Br Cl Br
A) Br2/FeBr3
B) CuBr
C) NaOH
D) H3PO2
E) H3PO4
Ans: D

Section: 20.10 & 20.11
75. Which one of the following is the best synthesis for 3,5-dibromotoluene?
A) toluene, Br2/FeBr3 excess
B) 1. p-toluidine, Br2/ FeBr3;
2. NaNO2/HCl, <5°C
3. H3PO2
C) 1. Toluene, HNO3/H2SO4
2. NH3
3. NaNO2/HCl, <5°C
4. CuBr
D) m-dibromobenzene, CH3Cl/AlCl3
E) m-bromotoluene, HNO3, H2SO4
2. Fe/HCl
3. NaNO2/HCl, <5°C
4. CuBr
Ans: B

Section: 23.10 & 23.11
O
COH
Cl
F
Ans: 1. CH3CH2Cl/AlCl3
2. HNO3/H2SO4
3. Cl2/FeCl3
4. Fe/HCl
5. NaNO2/HCl/<50C
6. HBF4
7. Na2Cr2O7/H2SO4/H2O

Section: 23.10 & 23.11
OCH3
CCH2CH3
O
Ans: O
1. CH3CH2CCl / AlCl3
2. HNO3/H2SO4
3. Fe/HCl
4. NaNO2/HCl/<50C
5. CH3OH/heat

Section: 23.10 & 23.11
OCH2CH3
Br
Ans: 1. HNO3/H2SO4
2. Br2/FeBr3
3. Fe/HCl
4. NaNO2/HCl/<50C
5. CH3CH2OH/heat

Section: 23.10 & 23.11
OH
NO 2
Ans: 1. HNO3/H2SO4
2. Fe/HCl
O
3. CH3CCl
4. HNO3/H2SO4
5. H3O+
6. NaNO2/HCl/<50C
7. H2O/heat

Section: 23.10 & 23.11
OH
Ans:
N N Cl
NO2 NH2
HNO3/H2SO4 Sn/HCl NaNO2/HCl
<50C
OH OH
exess
H2O fuming H2SO4 (CH3)2CHCl/AlCl3

OH
SO3H OH
H3O+
SO3H

Section: 23.10 & 23.11
O
COH
CN
Ans: CH2CH3 CH2CH3
CH3CH2Cl/AlCl3 HNO3/H2SO4 Na2Cr2O7/H2SO4/H2O
O O O O
NO2
COH COH COH COH
Fe/HCl NaNO2/HCl CuCN

0
<5 C
NO2 NH2 N N Cl CN

Section: 23.10 & 23.11
O
NH2 COH
Br Br
CH3
Br
Ans:
N N Cl
NH2 NH2
Br Br Br Br
Br2/ FeBr3 NaNO2/HCl H3PO2
excess < 50 C
CH3 CH3
CH3
Br Br
Br Br
Br Br
1. KMnO4/NaOH/H2O
2. H3O+ O
CH3
Br OH
Br

Section: 23.10 & 23.11
83. Provide a stepwise synthesis to carry out the following conversion.
CH2NH2
O
Ans: NO2 NH2
CH3CH2CCl HNO3/H2SO4 Fe/HCl
AlCl3
O O
O
N N Cl CN CN
Zn(Hg)/HCl 1. LiAlH4
NaNO2/HCl CuCN
2. H3O+
0
<5 C
O O
CH2NH2

Section: 23.10 & 23.11
84. Provide a stepwise synthesis to carry out the following conversion.
I
Br Br
Ans: O
NO2 NH2 NHCCH3

O
HNO3/H2SO4 Sn/HCl CH3CCl fuming H2SO4
O
O
NHCCH3 NH2
NHCCH3
Br Br
excess Br Br
Br2/FeBr3 H3O+ NaNO2/HCl
heat <50C
N Cl SO3H
SO3H
N I
Br Br Br Br
CuI

Section: 23.10 & 23.11
NH2
Br
Br Br
Br Br
NO2
Ans: 1. NaNO2/HCl/<50C
2. CuBr
3. Fe/HCl
4. NaNO2/HCl/<50C
5. H3PO2

Section: 23.10 &23.11

OCH2CH3
CH3
NH2
NaNO2/HCl
2
< 50 C
Ans:
N
N OCH2CH3
CH3

Section: 23.10 &23.11
87. Predict the major product when p-toluidine reacts with sodium nitrite and hydrochloric
acid at <5C followed by o-ethylphenol?
2
Ans:
N
N OH
Section: 23.10 &23.11

N(CH3)2
NaNO2/HCl
NH2
< 50C
N(CH3)2 N(CH3)2
N
N
N N(CH3)2
N
I II
III
O2N N(CH3)2
2
IV
A) I
B) II
C) III
D) IV
E) None of these
Ans: B

Section: 23.10 &23.11
NaNO2/HCl 4-ethylphenol
4-chloroaniline
<50C
Ans:
N
N
OH
Cl

Section: 23.10 &23.11

CH3
N(CH3)2
N
N
Cl
CH3
Ans:
N
N
N(CH3)2

Section: 23.10 &23.11
Cl
N
N
OCH3
Cl
Ans: Cl Cl
Cl2/FeCl3 HNO3/H2SO4 Fe/HCl
Cl OCH3
Cl
NO2 NH2
NaNO2/HCl
< 50 C
N N Cl
N
N
OCH3
Topic: Nitrogen Heterocycles

Section: 23.12
Br2
0 0C
N
H
Br
Br Br
N N N N N
H H H
V
III IV
I Br II Br
A) I
B) II
C) III
D) IV
E) V
Ans: D

Section: 23.12

Br2
0 0C
N
H
Br
Br
Br N
N N N N
H H H
III IV Br
I Br II V
A) I
B) II
C) III
D) IV
E) V
Ans: D

Section: 23.12
94. Predict the major product when pyridine is treated with a mixture of nitric acid and
sulfuric acid.
A) 3-nitropyridine
B) 2-nitropyridine
C) 4-nitropyridine
D) 2,3-dinitropyridine
E) 4-aminopyridine
Ans: A
Topic: Spectroscopy
Section: 23.13
95. A compound with molecular formula C8H10BrN exhibits a singlet at 1.2 (I=2), a triplet
at 2.8 (I=2), a triplet at 3.0 (I=2), a doublet at 7.1 (I=2) and a doublet at 7.4 (I=2)
in its 1HNMR spectrum. Its IR spectrum shows two medium absorption bands near 3400
cm-1. What is the structure for this compound?
NH2 NH2
NH2 Br Br
NH2
Br
I Br
II III IV V
NH2
Br
A) I
B) II
C) III
D) IV
E) V
Ans: A
Topic: Spectroscopy
Section: 23.13
96. A compound with molecular formula C8H19N exhibits a triplet at 0.9 (I=6), a singlet at
1.1 (I=1), a sextet at 1.3 (I=4), a quintett at 1.4 (I=4) and a triplet at 2.6 (I=4) in
its 1HNMR spectrum. Its IR spectrum shows a medium absorption band near 3400 cm-1.
Its 13CNMR spectrum showed peaks at 13.7, 20.5, 30.4 and 49.2. What is the structure
for this compound?
Ans: H
N
Topic: Spectroscopy
Section: 23.13
97. A compound with molecular formula C4H11N exhibits a triplet at 0.9 (I=3), a doublet
at 1.1 (I=3), a quintet at 1.4 (I=2), a singlet at 1.7 (I=2) and a sextet at 2.8 (I=2)
in its 1HNMR spectrum. Its IR spectrum shows two medium absorption bands near
3400 cm-1. What is the structure for this compound?
Ans:
NH2
Topic: Spectroscopy
Section: 23.13
98. A compound with molecular formula C7H17N exhibits a triplet at 1.0 (I=3), a doublet
at 1.1 (I=6), a multiplet at 2.0 (I=1), a singlet at 2.3 (I=3), a doublet at 2.3 (I=2),
and a quartet at 2.4 (I=2) in its 1HNMR spectrum. Its 13CNMR spectrum showed
peaks at 13.4, 20, 27.9, 39.3, 49.5 and 65.2. What is the structure for this compound?
Ans:
N
Topic: Spectroscopy
Section: 23.13
99. A compound with molecular formula C6H15N displays the following IR, 1H NMR and
13
C NMR spectra. Propose a structure for this compound.
SDBS
Ans: H
N
Topic: Spectroscopy
Section: 23.13
100. A compound with molecular formula C8H11N displays the following IR, 1H NMR and
13
C NMR spectra. Propose a structure for this compound.
140 120 100 80 60 40 20 0

PPM
SDBS
Ans: NH2

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Chapter Twenty Three

Topic: Classification of amines

1. Which of the following is a primary amine?

Topic: Classification of amines

2. Which of the following is a secondary amine?

Topic: Classification of amines

3. Which of the following is a tertiary amine?

Topic: Classification of amines

Topic: Classification of amines

5. Classify the following compounds as a primary, secondary or tertiary amine.

Topic: Nomenclature of amines

6. What is the structure for 1-butanamine?

Topic: Nomenclature of amines

Topic: Nomenclature of amines

8. What is the common name for the following compound?

Topic: Nomenclature of amines

9. What is the common name for the following compound?

Topic: Nomenclature of amines

Topic: Nomenclature of amines

11. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

Topic: Nomenclature of amines

13. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

14. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

15. What is the structure for 3-chloro-N-ethylpentanamine?

Topic: Nomenclature of amines

16. What is the structure for N-ethylbenzylamine?

Topic: Nomenclature of amines

17. What is the structure for N,N-diethylaniline?

Topic: Nomenclature of amines

18. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

19. What is the IUPAC name for the following compound?

20. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

21. What is the IUPAC name for the following compound?

Topic: Nomenclature of amines

22. What is the IUPAC name for the following compound?

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

25. Which of the following compounds is most soluble in water?

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

28. Which of the following compounds is the strongest base?

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Properties of amines

Topic: Preparation of amines

Topic: Preparation of amines

39. Predict the product for the following reaction.

Topic: Preparation of amines

Topic: Preparation of amines