Deck 13: Alkynes: the Carbon
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Deck 13: Alkynes: the Carbon
1
What would be the proper name of the following compound? 
A) 1,1-dimethyl-2-propyn-1-ol
B) 3-methyl-1-butyn-3-ol
C) 3-hydroxy-3-methyl-1-propyne
D) 2-methyl-3-butyn-2-ol
E) 2-ethynyl-2-propanol

A) 1,1-dimethyl-2-propyn-1-ol
B) 3-methyl-1-butyn-3-ol
C) 3-hydroxy-3-methyl-1-propyne
D) 2-methyl-3-butyn-2-ol
E) 2-ethynyl-2-propanol
2-methyl-3-butyn-2-ol
2
What would be the product of the following reaction? 
A)
B)

C)

D)

E)


A)
B)

C)

D)

E)


3
Considering the mechanism of the following reaction,which of the intermediates shown below is not likely to form along the reaction pathway? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)


4
What organic product results from the reaction shown below? 
A) CH4
B) Ca(CH3)2
C) CH3CH3 + Ca(OH)2
D)

E)


A) CH4
B) Ca(CH3)2
C) CH3CH3 + Ca(OH)2
D)

E)

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5
What is the major product of the following reaction? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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6
What would be the product of the following reaction? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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7
Given separate pure samples,in what way(s)could you quickly distinguish between the two alkynes below? 
A) gas chromatography
B) infrared spectroscopy
C) ultraviolet spectroscopy
D) NMR spectroscopy
E) both B and D

A) gas chromatography
B) infrared spectroscopy
C) ultraviolet spectroscopy
D) NMR spectroscopy
E) both B and D
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8
What is NaNH2 mainly used for in organic chemistry?
A) as a nucleophile
B) as a weak base
C) as a strong base
D) as a weak acid
E) as a strong acid
A) as a nucleophile
B) as a weak base
C) as a strong base
D) as a weak acid
E) as a strong acid
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9
What is the major product expected from the following reaction? 
A)
B)

C)

D)

E)


A)
B)

C)

D)

E)

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10
What major product(s)are expected from the reaction shown below? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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11
What would you expect the major product of the following reaction sequence to be? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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12
What would be the product of the following reaction sequence? 
A)
B)

C)

D)

E)


A)
B)

C)

D)

E)

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13
Which metal acts as a poison for hydrogenation catalysts?
A) Pd
B) Pt
C) Ni
D) Pb
E) Hg
A) Pd
B) Pt
C) Ni
D) Pb
E) Hg
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14
What would be the major product of the following reaction? 
A)
B)

C)

D)

E)


A)
B)

C)

D)

E)

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15
What major product(s)are expected from the reaction shown below? 
A)
B)

C)

D)

E) more than one of the above

A)
B)

C)

D)

E) more than one of the above
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16
What would be the product of the following reaction sequence? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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17
What reagent(s)would be required to accomplish the transformation shown? 
A) H2,Pt
B) H2,Lindlar's catalyst
C) Na,liq.NH3,then H2O
D) LiAlH4 then H2O
E) None of these reagents would accomplish this transformation.

A) H2,Pt
B) H2,Lindlar's catalyst
C) Na,liq.NH3,then H2O
D) LiAlH4 then H2O
E) None of these reagents would accomplish this transformation.
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18
Which,if either,of the following hydrogenations would be the more exothermic? 
A) Step 1
B) Step 2
C) both are equally exothermic
D) neither is exothermic
E) there is no way to predict this

A) Step 1
B) Step 2
C) both are equally exothermic
D) neither is exothermic
E) there is no way to predict this
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19
What reactant and product types would be most appropriate for the reagents shown? 
A) alkene/Markovnikov alcohol
B) alkene/anti-Markovnikov alcohol
C) alkyne/aldehyde or ketone
D) both A and B
E) both B and C

A) alkene/Markovnikov alcohol
B) alkene/anti-Markovnikov alcohol
C) alkyne/aldehyde or ketone
D) both A and B
E) both B and C
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20
What would be the major product expected from the following reaction? (Notice the D isotope.) 
A)
B)

C)

D)

E)


A)
B)

C)

D)

E)

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21
What reagent(s)would be required to accomplish the transformation shown? 
A) H2,Pt
B) H2,Lindlar's catalyst
C) Na,liq.NH3,then H2O
D) LiAlH4 then H2O
E) None of the above reagents would accomplish this transformation.

A) H2,Pt
B) H2,Lindlar's catalyst
C) Na,liq.NH3,then H2O
D) LiAlH4 then H2O
E) None of the above reagents would accomplish this transformation.
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22
Which product is the most likely to form? 
A)

B)

C)

D)

E) All of the above will form in nearly equal amounts.

A)

B)

C)

D)

E) All of the above will form in nearly equal amounts.
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23
What is the expected product from the following reaction? 
A)

B)

C)

D)

E) no reaction

A)

B)

C)

D)

E) no reaction
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24
The following is an example of intramolecular Heck reaction.Which product is the most likely to form? 
A)

B)

C)

D)

E)


A)

B)

C)

D)

E)

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25
What is the major product from the following reaction? 
A)

B)

C)

D)

E) no reaction

A)

B)

C)

D)

E) no reaction
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26
What is the major product of the following reaction? 
A) H3C-C C-CH2D
B) H3C-C C-CHD2
C) DH2C-C C-CH2D
D) D3C-C C-CD3
E) no reaction

A) H3C-C C-CH2D
B) H3C-C C-CHD2
C) DH2C-C C-CH2D
D) D3C-C C-CD3
E) no reaction
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27
Infrared spectroscopy is a useful technique in identifying terminal alkynes.What is/are the characteristic stretching band(s)for a terminal alkyne?
A) 3260-3330 cm-1
B) 1550-1680 cm-1
C) 2100-2260 cm-1
D) both A and B
E) both A and C
A) 3260-3330 cm-1
B) 1550-1680 cm-1
C) 2100-2260 cm-1
D) both A and B
E) both A and C
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