Deck 7: The Reactions of Alkynes - Introduction to Multistep Synthesis
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Deck 7: The Reactions of Alkynes - Introduction to Multistep Synthesis
1
What is the common name for the following alkyne? 
A)neohexyne
B)trimethylpropyne
C)trimethylacetylene
D)tert-butylacetylene
E)isopropylacetylene

A)neohexyne
B)trimethylpropyne
C)trimethylacetylene
D)tert-butylacetylene
E)isopropylacetylene
tert-butylacetylene
2
Give the IUPAC name for the following compound. 
A)isoprene
B)3-methyl-1,3-butadiene
C)2-methyl-1,3-butadiene
D)2-methyl-2,3-butadiene
E)isobutadiene

A)isoprene
B)3-methyl-1,3-butadiene
C)2-methyl-1,3-butadiene
D)2-methyl-2,3-butadiene
E)isobutadiene
2-methyl-1,3-butadiene
3
Draw an acceptable structure for acetylene.
H-C
C-H

4
Name the following compound. 

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5
Provide an acceptable name for the compound shown. 

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6
How many distinct internal alkynes exist with a molecular formula of C6H10?
A)1
B)2
C)3
D)4
E)5
A)1
B)2
C)3
D)4
E)5
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7
Give the IUPAC name for BrCH2CH2CCCH2CH3.
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8
Write structures and give IUPAC names for all alkynes with molecular formula C5H8.
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9
Give the IUPAC name for HCCCH2CH2CH3.
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10
What is the IUPAC name for the following alkyne? 
A)5-Bromo-2-heptyne
B)3-Bromo-5-heptyne
C)2-Bromo-2-methyl-4-hexyne
D)5-Bromo-5,5-dimethylhexyne
E)5-Bromo-5-methyl-2-hexyne

A)5-Bromo-2-heptyne
B)3-Bromo-5-heptyne
C)2-Bromo-2-methyl-4-hexyne
D)5-Bromo-5,5-dimethylhexyne
E)5-Bromo-5-methyl-2-hexyne
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11
Give the systematic name of the compound shown below. 

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12
Provide the structure of all distinct terminal alkynes with a molecular formula of C6H10.
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13
Name the following compound. 
A)3-heptyn-6-ol
B)3-hepten-6-ol
C)4-hepten-2-ol
D)4-heptyn-2-ol
E)4-heptan-2-ol

A)3-heptyn-6-ol
B)3-hepten-6-ol
C)4-hepten-2-ol
D)4-heptyn-2-ol
E)4-heptan-2-ol
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14
Provide the systematic name of the compound shown. 

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15
Draw an acceptable structure for 3-sec-butyl-1-heptyne.
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16
How many distinct terminal alkynes exist with a molecular formula of C5H8?
A)1
B)2
C)3
D)4
E)5
A)1
B)2
C)3
D)4
E)5
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17
Give the IUPAC name for (CH3)2C(CH2CH3)CCCH(CH3)2.
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18
Give the systematic name for the alkyne Cl3CCH2CH2CCCH3.
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19
Draw an acceptable structure for 2-hexyne.
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20
What is the IUPAC name for the following compound? 
A)cis,trans-2,4-heptadiene
B)2Z,4Z-2,4-heptadiene
C)cis,cis-2,4-heptadiene
D)trans,trans-2,4-heptadiene
E)2E,4E-2,4-heptadiene

A)cis,trans-2,4-heptadiene
B)2Z,4Z-2,4-heptadiene
C)cis,cis-2,4-heptadiene
D)trans,trans-2,4-heptadiene
E)2E,4E-2,4-heptadiene
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21
What are the hybridizations of the carbon atoms numbered 1 and 2 in the structure below? 1 2
H3C-CH
CH-C
C-H
A)sp3,sp2
B)sp2,sp2
C)sp2,sp
D)sp,sp
H3C-CH


A)sp3,sp2
B)sp2,sp2
C)sp2,sp
D)sp,sp
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22
________ is produced when 1 equivalent of HBr is added to 1-hexyne.
A)2-bromo-1-hexene
B)E-1-bromo-1-hexene
C)Z-1-bromo-1-hexene
D)A mixture of E and Z isomers of 1-bromo-1-hexene
E)E-2-bromo-2-hexene
A)2-bromo-1-hexene
B)E-1-bromo-1-hexene
C)Z-1-bromo-1-hexene
D)A mixture of E and Z isomers of 1-bromo-1-hexene
E)E-2-bromo-2-hexene
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23
Although you might expect 1-propyne to be more reactive than 1-propene in electrophilic addition reactions,the reverse is true.Explain this using your knowledge of the mechanism of electrophilic additions to both alkynes and alkenes.
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24
Provide the systematic name of the compound shown. 

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25
Which of the following improperly describes the physical properties of an alkyne?
A)relatively nonpolar
B)nearly insoluble in water
C)less dense than water
D)insoluble in most organic solvents
A)relatively nonpolar
B)nearly insoluble in water
C)less dense than water
D)insoluble in most organic solvents
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26
In the addition of hydrogen bromide to alkynes in the absence of peroxides,which of the following species is believed to be an intermediate?
A)vinyl anion
B)vinyl cation
C)vinyl radical
D)carbene
E)bromonium ion
A)vinyl anion
B)vinyl cation
C)vinyl radical
D)carbene
E)bromonium ion
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27
The carbon-carbon triple bond of an alkyne is composed of
A)three σ bonds.
B)two σ bonds and one π bond.
C)one σ bond and two π bonds.
D)three π bonds.
A)three σ bonds.
B)two σ bonds and one π bond.
C)one σ bond and two π bonds.
D)three π bonds.
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28
Provide the structure of the major organic product of the following reaction. 

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29
Provide the structure of the major organic product of the following reaction. 

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30
Which of the following statements correctly describes the general reactivity of alkynes?
A)An alkyne is an electron-rich molecule and therefore reacts as a nucleophile.
B)The σ bonds of alkynes are higher in energy than the π bonds and are thus more reactive.
C)Unlike alkenes,alkynes fail to undergo electrophilic addition reactions.
D)Alkynes are generally more reactive than alkenes.
E)Alkynes react as electrophiles,whereas alkenes reacts as nucleophiles.
A)An alkyne is an electron-rich molecule and therefore reacts as a nucleophile.
B)The σ bonds of alkynes are higher in energy than the π bonds and are thus more reactive.
C)Unlike alkenes,alkynes fail to undergo electrophilic addition reactions.
D)Alkynes are generally more reactive than alkenes.
E)Alkynes react as electrophiles,whereas alkenes reacts as nucleophiles.
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31
Name the following compound. 

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32
Give the systematic name of the compound shown below. 

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33
Which of the following statements is not true about propyne,HC
C-CH3?
A)It contains six sigma bonds.
B)It contains three pi bonds.
C)The H-C-H bond angle is about 109.5°.
D)The C-C-C bond angle is 180°.
E)The pi bond is weaker than the sigma bond.

A)It contains six sigma bonds.
B)It contains three pi bonds.
C)The H-C-H bond angle is about 109.5°.
D)The C-C-C bond angle is 180°.
E)The pi bond is weaker than the sigma bond.
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34
What are the hybridizations of the carbon atoms numbered 1 and 2 respectively in the following structure? 
A)sp3,sp2
B)sp2,sp2
C)sp,sp
D)sp2,sp
E)sp,sp2

A)sp3,sp2
B)sp2,sp2
C)sp,sp
D)sp2,sp
E)sp,sp2
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35
Provide the structure of (2E,4E)-2-chloro-2,4-octadiene.
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36
Which of the following compounds is the major product when 1-hexyne is treated with excess HBr?
A)1,1-dibromohexane
B)1,1-dibromohexene
C)1,2-dibromohexene
D)1,2-dibromohexane
E)2,2-dibromohexane
A)1,1-dibromohexane
B)1,1-dibromohexene
C)1,2-dibromohexene
D)1,2-dibromohexane
E)2,2-dibromohexane
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37
Provide the structure of the major organic product(s)in the reaction below. 

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38
Which of the following is the best synthesis of 2,2-dibromopropane? 
A)CH3CH
CH2 
B)CH3CH
CH2 
C)CH3C
CH 
D)CH3C
CH 
E)CH3CH
CH2 

A)CH3CH


B)CH3CH


C)CH3C


D)CH3C


E)CH3CH


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39
What two atomic orbitals or hybrid atomic orbitals overlap to form the carbon-carbon σ bond in ethyne?
A)sp3-sp3
B)p-p
C)sp2-sp2
D)s-s
E)sp-sp
A)sp3-sp3
B)p-p
C)sp2-sp2
D)s-s
E)sp-sp
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40
What is the major product of the following reaction? CH3C
CH 
A)
B)
C)CH3CH
CH-Cl
D)
E)


A)

B)

C)CH3CH

D)

E)

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41
Which of the following are enol forms of 2-butanone? 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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42
Give the major organic product for the reaction. 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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43
Provide the structure of the major organic product that results when 2-butyne is treated with 1 equivalent of HCl.
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44
Which of the following is the final and major product of this reaction? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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45
Provide the structure of the major organic product(s)in the reaction below. 

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46
Provide the major organic product in the reaction below. 

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47
Provide the structure of the major organic product of the following reaction. 

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48
Provide the major organic product in the reaction below. 

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49
Provide the structure of the major organic product that results when 2-butyne is treated with 2 equivalents of HCl.
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50
Give the major organic product for the reaction. 
A)
B)
C)
D)
E)

A)

B)

C)

D)

E)

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51
Provide the major organic product in the reaction below. 

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52
For the reaction below indicate whether the equilibrium constant will be greater than 1 or less than 1. 

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53
Provide the structure of the intermediate which forms in the first step of the reaction of 1-butyne with water in the presence of H2SO4/HgSO4.
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54
Provide the major organic product in the reaction below. 

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55
Provide the structure of the major organic product that results when 2-butyne is treated with 1 equivalent of Br2.
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56
Provide the major organic product in the reaction below. 

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57
Provide the major organic product in the reaction below. 

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58
Give the best reagents for the reaction. 
A)H2SO4,HgSO4,HgSO4
B)1)disiamylborane,2.HO-,H2O,H2O2
C)K2Cr2O7,H+
D)NaOCl
E)H2,Pd

A)H2SO4,HgSO4,HgSO4
B)1)disiamylborane,2.HO-,H2O,H2O2
C)K2Cr2O7,H+
D)NaOCl
E)H2,Pd
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59
Give the major organic product for the reaction. 
A)
B)
C)
D)CH3CH2CH2CH
CHOH
E)

A)

B)

C)

D)CH3CH2CH2CH

E)

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60
Which of the following is the final and major product of this reaction? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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61
Provide the structure of the major organic product of the following reaction. 

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62
Which of the alkyne addition reactions below involves an enol intermediate?
A)hydroboration/oxidation
B)treatment with HgSO4 in dilute H2SO4
C)hydrogenation
D)both A and B
E)both A and C
A)hydroboration/oxidation
B)treatment with HgSO4 in dilute H2SO4
C)hydrogenation
D)both A and B
E)both A and C
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63
A mixture of 1-heptyne,2-heptyne,and 3-heptyne was hydrogenated in the presence of a platinum catalyst until hydrogen uptake ceased.If one assumes that the hydrogenation went to completion,how many distinct seven-carbon hydrocarbons were produced?
A)1
B)2
C)3
D)6
E)8
A)1
B)2
C)3
D)6
E)8
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64
Provide the structure of the major organic product(s)in the reaction below. 

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65
Provide the structure of the major organic product that results when 2-butyne is treated with HgSO4/H2SO4 in water.
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66
Provide the structure of the major organic product of the following reaction. 

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67
Provide the structure of the major organic product of the following reaction. 

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68
In the reduction of alkynes using sodium in liquid ammonia,which of the species below is not an intermediate in the commonly accepted mechanism?
A)vinyl anion
B)vinyl radical
C)radical anion
D)vinyl cation
A)vinyl anion
B)vinyl radical
C)radical anion
D)vinyl cation
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69
The reagent needed to convert 2-butyne to trans-2-butene is
A)H2/Pt.
B)H2/Lindlar's catalyst.
C)Li/NH3.
D)Na/NH3.
E)C or D.
A)H2/Pt.
B)H2/Lindlar's catalyst.
C)Li/NH3.
D)Na/NH3.
E)C or D.
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70
An optically active compound (A),C6H10,reacts with H2/Ni to produce compound (B),C6H14.(B)is optically inactive.Deduce the structures of (A)and (B).
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71
Give the best reagents for the reaction. 
A)H2SO4,HgSO4,HgSO4
B)1)disiamylborane,2.HO-,H2O,H2O2
C)K2Cr2O7,H+
D)NaOCl
E)H2,Pd

A)H2SO4,HgSO4,HgSO4
B)1)disiamylborane,2.HO-,H2O,H2O2
C)K2Cr2O7,H+
D)NaOCl
E)H2,Pd
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72
Provide the structure of the major organic product of the following reaction. 

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73
Provide the structure of the major organic product(s)in the reaction below.
CH3CH2-C
C-CH3 
CH3CH2-C


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74
The reagent needed to convert 2-butyne to cis-2-butene is
A)H2/Pt.
B)H2/Lindlar's catalyst.
C)Li/NH3.
D)Na/NH3.
E)H+/Zinc dust.
A)H2/Pt.
B)H2/Lindlar's catalyst.
C)Li/NH3.
D)Na/NH3.
E)H+/Zinc dust.
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75
Complete the following reaction.
3-hexyne
3-hexyne

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76
Provide the structure of the major organic product(s)in the reaction below. 

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77
Give the major organic product for the reaction. 
A)
B)
C)
D)CH3CH2CH2CH
CHOH
E)

A)

B)

C)

D)CH3CH2CH2CH

E)

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78
Provide the major organic product in the reaction below. 

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79
Complete the following reaction. 

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80
Provide the major organic product in the reaction below. 

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