QOI 0809 C=C

Name___________________________________
ESSAY. Write your answer in the space provided or on a separate sheet of paper.
1) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
2) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
3) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
4) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
5) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
6) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
1
7) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
8) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
9) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
10) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
11) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
12) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
13) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
2
14) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
15) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
16) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
17) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
(Z)-3-hexene
1. BH
3
THF
2. H
2
O
2
, -OH

18) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
19) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
20) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
3
21) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
22) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
23) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
24) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
25) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
26) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
27) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
4
28) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
29) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
30) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
31) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
32) Draw the major organic product generated in the reaction below. Pay particular attention to regio- and
stereochemical detail.
33) Humulene is a monocyclic terpene constituent of carnations. When 0.25 mol of humulene is hydrogenated in
the presence of platinum catalyst, 0.75 mol of H
2
reacts with the humulene to produce a monocyclic
hydrocarbon of formula C
15
H
30
. What is the molecular formula of humulene?
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
34) Treatment of cyclopentene with peroxybenzoic acid __________.
A) gives the same product as treatment of cyclopentene with OsO
4
B) results in oxidative cleavage of the ring to produce an acyclic compound
C) yields an equimolar mixture of enantiomeric epoxides
D) yields a meso epoxide
E) none of the above
34)
5
ESSAY. Write your answer in the space provided or on a separate sheet of paper.
35) Complete the following reaction and provide a detailed, step-by-step mechanism for the process.
36) Complete the following reaction and provide a detailed, step-by-step mechanism for the process.
37) Complete the following reaction and provide a detailed, step-by-step mechanism for the process.
38) Provide a detailed, step-by-step mechanism for the reaction shown below.
39) Provide a detailed, step-by-step mechanism for the reaction shown below.
40) When isobutylene [CH
2
C(CH
3
)
2
] is treated with BF
3
, polyisobutylene is formed. Provide a step-by-step
mechanism for this polymerization reaction.
41) Provide the reagents necessary to complete the following transformation.
42) Provide the reagents necessary to complete the following transformation.
6
43) Provide the reagents necessary to complete the following transformation.
44) Provide the reagents necessary to complete the following transformation.
45) Provide the reagents necessary to convert 3-methyl-2-butanol to 2-methyl-2-butanol.
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
46) Both (E)- and (Z)-hex-3-ene can be subjected to a hydroboration-oxidation sequence. How are the
products from these two reactions related to each other?
A) The products of the two isomers are not structurally related.
B) The products of the two isomers are related as constitutional isomers.
C) The (E)- and (Z)-isomers generate the same products in exactly the same amounts.
D) The products of the two isomers are related as diastereomers.
E) The (E)- and (Z)-isomers generate the same products but in differing amounts.
46)
47) Both (E)- and (Z)-hex-3-ene can be treated with D
2
in the presence of a platinum catalyst. How
are the products from these two reactions related to each other?
A) The (E)- and (Z)-isomers generate the same products but in differing amounts.
B) The (E)- and (Z)-isomers generate the same products in exactly the same amounts.
C) The products of the two isomers are related as enantiomers.
D) The products of the two isomers are related as constitutional isomers.
E) The products of the two isomers are related as diastereomers.
47)
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
48) Give the structure of the alkene which would yield the following products upon
ozonolysis-reduction.
CH
3
CH
2
CH
2
CH
2
CHO + CH
2
O
48)
49) Give the structure of the alkene which would yield the following products upon
ozonolysis-reduction.
CH
3
COCH
3
+ CH
3
CH
2
CHO
49)
7
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
50) Addition of Br
2
to (E)-hex-3-ene produces __________.
A) a mixture of enantiomeric dibromides which is optically inactive
B) a meso dibromide
C) (E)-3,4-dibromo-3-hexene
D) (Z)-3,4-dibromo-3-hexene
E) a mixture of enantiomeric dibromides which is optically active
50)
ESSAY. Write your answer in the space provided or on a separate sheet of paper.
51) The following reaction is known to proceed by a free radical chain mechanism. Suggest a reasonable,
step-by-step mechanism for this reaction.
CH
3
CHCH
2
+ CHCl
3

ROOR
CH
3
CH
2
CH
2
CCl
3
52) Consider how the ICl bond is polarized and predict the product which results when this mixed halogen adds
to 1-methylcyclohexene.
53) -Ocimene is a natural product with a pleasant odor. Based on the information below, deduce the structure of
-ocimene.
54) Based on the relative stabilities of the intermediates involved, explain the basis for Markovinkov's rule in the
addition of hydrogen halides to alkenes.
55) Explain the regioselectivity observed in the radical addition of HBr to 2-methylpropene.
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
56) The mechanism for the acid-catalyzed hydration of alkenes is simply the reverse of the
mechanism by which alcohols are dehydrated using concentrated acid. This is an
illustration of the principle of __________.
56)
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
57) Which of the following is the best reaction sequence to use if one wants to accomplish a
Markovnikov addition of water to an alkene with minimal skeletal rearrangement?
A) water + dilute acid
B) oxymercuration-demercuration
C) hydroboration-oxidation
D) water + concentrated acid
E) none of the above
57)
8
ESSAY. Write your answer in the space provided or on a separate sheet of paper.
58) Draw the Lewis structure of dibromocarbene.
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
59) Which of the following additions to alkenes occur(s) specifically in an anti fashion?
A) addition of H
2
B) addition of H
2
O in dilute acid
C) addition of Br
2
D) hydroboration-oxidation
E) both A and B
59)
60) Which of the following additions to alkenes occur(s) specifically in an syn fashion?
A) addition of H
2
B) dihydroxylation using OsO
4
, H
2
O
2
C) hydroboration
D) addition of HCl
E) A, B, and C
60)
61) HBr can be added to an alkene in the presence of peroxides (ROOR). What function does the
peroxide serve in this reaction?
A) electrophile
B) acid catalyst
C) radical chain initiator
D) nucleophile
E) solvent
61)
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
62) Name the major product which results when HBr is added to 3-ethyl-3-hexene. 62)
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
63) Which of the following intermediates is thought to occur in the mechanism by which alkenes are
hydrated in the presence of acid?
A) free radical
B) carbene
C) carbocation
D) alkyne
E) carbanion
63)
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
64) Name the major alcohol product which results when 3,3-dimethylbut-1-ene is treated
with dilute acid.
64)
9
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
65) What synthetic goal is achieved by subjecting an alkene to an oxymercuration-demercuration
sequence?
A) anti-Markovnikov addition of H
2
O wherein skeletal rearrangement is prevented
B) Markovnikov addition of H
2
O wherein skeletal rearrangement is promoted
C) anti-Markovnikov addition of H
2
O wherein skeletal rearrangement is promoted
D) syn-hydroxylation
E) Markovnikov addition of H
2
O wherein skeletal rearrangement is prevented
65)
66) When an alkene is subjected to treatment with Hg(OAc)
2
in alcohol followed by reaction with
NaBH
4
, what new class of compound is formed?
A) syn diol B) alkane C) epoxide D) ether E) alkyne
66)
67) Which of the following compounds is (are) appropriate to promote the cationic polymerization of
isobutylene?
A) BF
3
B) NaOH
C) H
2
SO
4
D) ROOR
E) both H
2
SO
4
and BF
3
67)
ESSAY. Write your answer in the space provided or on a separate sheet of paper.
68) Why can methyl acrylate (H
2
CCHCO
2
CH
3
) be polymerized through anionic polymerization?
69) Name the compound PhCO
3
H and give its most common use as a reagent.
70) Provide the structure of the product which results when the alkene below is treated with O
3
followed by
(CH
3
)
2
S.
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
71) Provide the structure of the major organic product of the reaction below. 71)
10
72) Provide the structure of the major organic product of the reaction below. 72)
73) Provide the structure of the major organic product of the reaction below. 73)
74) Provide the structure of the major organic product of the reaction below. 74)
75) Provide the structure of the major organic product of the reaction below. 75)
76) Provide the structure of the major organic product of the reaction below. 76)
77) Provide the structure of the major organic product of the reaction below. 77)
11
78) Provide the structure of the major organic product of the reaction below. 78)
79) Provide the structure of the major organic product of the reaction below. 79)
80) Provide the structure of the major organic product of the reaction below. 80)
81) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
81)
82) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
82)
83) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
83)
12
84) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
84)
85) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
85)
86) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
86)
87) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
87)
88) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
88)
89) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
89)
13
90) Draw the major organic product generated in the reaction below. Pay particular attention
to regio- and stereochemical detail.
90)
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
91) Which of the following alkenes will yield a meso dihalide when reacted with Br
2
/CCl
4
at room
temperature?
A)
B)
C)
D)
E) both Band D
91)
92) Acid catalyzed hydration (H
2
SO
4
/water/) of an unknown compound (A)with a chemical formula
C
6
H
12
, yielded a racemic mixture of product C
6
H
13
OH. Which, if any, of the following
compounds is/are possible structures for the initial compound (A)?
A) compounds 2 and 3
B) compound 2 only
C) compound 1 only
D) compounds 1 and 3
E) none of the above
92)
14
93) A reaction of an unknown alkene with MCPBA in dichloromethane followed by work-up with
H
2
O/H+ yielded, as the major product, a racemic mixture of (2S, 3S) and (2R,
3R)-3-methylpentan-2,3-diol. What is the specific structure of the alkene used in the reaction?
A) (E)-3-methylpent- 2-ene
B) 2-methylpent-2-ene
C) (Z)-3-methylpent-2-ene
D) 2,3-dimethylbut-2-ene
E) none of the above
93)
SHORT ANSWER. Write the word or phrase that best completes each statement or answers the question.
94) When 3,6-dimethylcyclohexene is reacted with dry gaseous HBr, one of the products is
1-bromo-1,4-dimethylcyclohexane. Provide a detailed step-by-step mechanism to
explain the formation of this product
94)
MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.
95) Treatment of 2-methylpropene with which of the following reaction conditions results in an
anti-Markovnikov addition product?
A) dry gaseous HBr with peroxides present
B) BH
3
-THF, followed by alkaline H
2
O
2
C) aqueous Hg(OAc)
2
, followed by alkaline NaBH
4
D) dilute H
2
SO
4
and heat
E) both A and B
95)
15
96) An unknown compound with empirical formula C
3
H
5
was treated with Br
2
/CCl
4
.

The bromine
solution went from orangish/red to clear immediately at room temperature. Upon treatment with
O
3
followed by work-up with dimethylsulfide the following products were identified. From the
information provided what is/are the most likely structure(s) for this unknown compound.
A)
B)
C)
D)
E) both A and D
96)
16
Answer Key
Testname: UNTITLED1
1)
ID: oc6w 8-1
Diff: 3
2)
ID: oc6w 8-2
Diff: 1
3)
ID: oc6w 8-3
Diff: 1
4)
ID: oc6w 8-4
Diff: 3
5)
ID: oc6w 8-5
Diff: 2
6)
ID: oc6w 8-6
Diff: 3
7)
ID: oc6w 8-7
Diff: 2
17
Answer Key
Testname: UNTITLED1
8)
ID: oc6w 8-8
Diff: 2
9)
ID: oc6w 8-9
Diff: 2
10)
ID: oc6w 8-10
Diff: 1
11)
ID: oc6w 8-11
Diff: 3
12)
ID: oc6w 8-12
Diff: 2
13)
ID: oc6w 8-13
Diff: 2
14)
ID: oc6w 8-14
Diff: 2
18
Answer Key
Testname: UNTITLED1
15)
ID: oc6w 8-15
Diff: 3
16)
ID: oc6w 8-16
Diff: 3
17)
ID: oc6w 8-17
Diff: 3
18)
ID: oc6w 8-18
Diff: 2
19)
ID: oc6w 8-19
Diff: 1
20)
ID: oc6w 8-20
Diff: 3
21)
ID: oc6w 8-21
Diff: 3
22)
ID: oc6w 8-22
Diff: 1
19
Answer Key
Testname: UNTITLED1
23)
ID: oc6w 8-23
Diff: 3
24)
ID: oc6w 8-24
Diff: 3
25)
ID: oc6w 8-25
Diff: 3
26)
ID: oc6w 8-26
Diff: 3
27)
ID: oc6w 8-27
Diff: 2
28)
ID: oc6w 8-28
Diff: 2
29)
ID: oc6w 8-29
Diff: 3
20
Answer Key
Testname: UNTITLED1
30)
ID: oc6w 8-30
Diff: 3
31)
ID: oc6w 8-31
Diff: 2
32)
ID: oc6w 8-32
Diff: 2
33) C
15
H
24
ID: oc6w 8-33
Diff: 2
34) D
ID: oc6w 8-34
Diff: 3
35)
ID: oc6w 8-35
Diff: 1
36)
ID: oc6w 8-36
Diff: 2
37)
ID: oc6w 8-37
Diff: 2
21
Answer Key
Testname: UNTITLED1
38)
ID: oc6w 8-38
Diff: 2
39)
ID: oc6w 8-39
Diff: 3
40)
ID: oc6w 8-40
Diff: 2
41) 1. Br
2
, h
2. H
2
O,
or
1. Br
2
, h
2. NaOCH
3
, CH
3
OH
3. H
3
O
+
or Hg(OAc)
2
, H
2
O; NaBH
4
ID: oc6w 8-41
Diff: 3
42) 1. NaOCH
3
, CH
3
OH
2. OsO
4
, H
2
O
2
or cold, dilute KMnO
4
,
-
OH
ID: oc6w 8-42
Diff: 2
43) 1. NaOCH
3
, CH
3
OH
2. MCPBA or CH
3
CO
3
H
3. H
3
O
+
or
-
OH
ID: oc6w 8-43
Diff: 3
22
Answer Key
Testname: UNTITLED1
44) 1. Br
2
, h
2. NaOCH
3
, CH
3
OH
3. CH
2
I
2
, Zn(Cu)
ID: oc6w 8-44
Diff: 3
45) 1. conc. H
2
SO
4
2. H
3
O
+
or Hg(OAc)
2
, H
2
O
or
1. PBr
3
2. NaOCH
3
, CH
3
OH
3. NaBH
4
ID: oc6w 8-45
Diff: 2
46) C
ID: oc6w 8-46
Diff: 2
47) E
ID: oc6w 8-47
Diff: 2
48) CH
3
CH
2
CH
2
CH
2
CHCH
2
ID: oc6w 8-48
Diff: 1
49) (CH
3
)
2
CCHCH
2
CH
3
ID: oc6w 8-49
Diff: 1
50) B
ID: oc6w 8-50
Diff: 2
51) ROOR 2 RO
RO + HCCl
3
ROH + CCl
3
Cl
3
C + CH
2
CHCH
3
Cl
3
CCH
2
CH

CH
3
Cl
3
CCH
2
CH

CH
3
+ HCCl
3
Cl
3
CCH
2
CH
2
CH
3
+ CCl
3
ID: oc6w 8-51
Diff: 3
52)
ID: oc6w 8-52
Diff: 3
23
Answer Key
Testname: UNTITLED1
53)
ID: oc6w 8-53
Diff: 2
54) The rate-determining step in this reaction is the production of a carbocation intermediate. Since this step is
endothermic, Hammond's postulate allows one to gauge the relative stabilites of the transition states by comparing the
relative stabilities of the carbocation intermediates. The reaction pathway which produces the more substituted
carbocation will thus occur more rapidly.
ID: oc6w 8-54
Diff: 2
55) The reaction proceeds via the addition of Br

to the alkene. Two competing pathways are possible, but the transition
state leading to the more substituted alkyl radical is lower in energy. This process ultimately makes the addition
anti-Markovnikov in nature.
ID: oc6w 8-55
Diff: 3
56) microscopic reversibility
ID: oc6w 8-56
Diff: 1
57) B
ID: oc6w 8-57
Diff: 1
58)
ID: oc6w 8-58
Diff: 3
59) C
ID: oc6w 8-59
Diff: 1
60) E
ID: oc6w 8-60
Diff: 1
61) C
ID: oc6w 8-61
Diff: 2
62) 3-bromo-3-ethylhexane
ID: oc6w 8-62
Diff: 2
63) C
ID: oc6w 8-63
Diff: 2
64) 2,3-dimethyl-2-butanol
ID: oc6w 8-64
Diff: 2
65) E
ID: oc6w 8-65
Diff: 2
24
Answer Key
Testname: UNTITLED1
66) D
ID: oc6w 8-66
Diff: 2
67) E
ID: oc6w 8-67
Diff: 2
68) The intermediate carbanion and the transition state leading to it are stabilized by the electron-withdrawing capacity of
the carbonyl group.
ID: oc6w 8-68
Diff: 2
69) peroxybenzoic acid; an oxidizing agent which converts alkenes to epoxides
ID: oc6w 8-69
Diff: 1
70)
ID: oc6w 8-70
Diff: 3
71)
ID: oc6w 8-71
Diff: 1
72)
ID: oc6w 8-72
Diff: 2
25
Answer Key
Testname: UNTITLED1
73)
ID: oc6w 8-73
Diff: 3
74)
ID: oc6w 8-74
Diff: 3
75)
ID: oc6w 8-75
Diff: 2
76)
ID: oc6w 8-76
Diff: 2
77)
ID: oc6w 8-77
Diff: 2
26
Answer Key
Testname: UNTITLED1
78)
ID: oc6w 8-78
Diff: 3
79)
ID: oc6w 8-79
Diff: 2
80)
ID: oc6w 8-80
Diff: 3
81)
ID: oc6w 8-81
Diff: 3
82)
ID: oc6w 8-82
Diff: 3
27
Answer Key
Testname: UNTITLED1
83)
ID: oc6w 8-83
Diff: 3
84)
ID: oc6w 8-84
Diff: 3
85)
ID: oc6w 8-85
Diff: 3
86)
ID: oc6w 8-86
Diff: 3
87)
ID: oc6w 8-87
Diff: 3
28
Answer Key
Testname: UNTITLED1
88)
ID: oc6w 8-88
Diff: 3
89)
ID: oc6w 8-89
Diff: 3
90)
ID: oc6w 8-90
Diff: 3
91) B
ID: oc6w 8-91
Diff: 2
92) E
ID: oc6w 8-92
Diff: 2
93) C
ID: oc6w 8-93
Diff: 3
94)
ID: oc6w 8-94
Diff: 3
29
Answer Key
Testname: UNTITLED1
95) E
ID: oc6w 8-95
Diff: 1
96) A
ID: oc6w 8-96
Diff: 2
30