Deck 14: Electrophilic Addition to Nonpolar Π Bonds 2: Reactions Involving Cyclic Transition States
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Deck 14: Electrophilic Addition to Nonpolar Π Bonds 2: Reactions Involving Cyclic Transition States
1
What reagent is required to complete the following reaction? 
A)CH2N2
B)NaOH
C)HCl
D)PCl3
E)Cl2

A)CH2N2
B)NaOH
C)HCl
D)PCl3
E)Cl2
NaOH
2
When a carbene reacts with an alkene,what functionality is created?
A)Cyclopropane ring
B)Oxetane
C)Epoxide
D)Alkyne
E)Alcohol
A)Cyclopropane ring
B)Oxetane
C)Epoxide
D)Alkyne
E)Alcohol
Cyclopropane ring
3
Carbenes react with alkenes utilizing which fundamental step?
A)Nucleophilic addition
B)Electrophilic addition
C)Nucleophile elimination
D)Electrophile elimination
E)SN2
A)Nucleophilic addition
B)Electrophilic addition
C)Nucleophile elimination
D)Electrophile elimination
E)SN2
Electrophilic addition
4
What is the product of the following 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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5
What is the product of the following 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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6
Carbenes are routinely created using alkenes plus which of the following molecules?
A)CH2N2
B)CH2Cl2
C)CH2Br2
D)All of the above (a-c)
E)None of the above
A)CH2N2
B)CH2Cl2
C)CH2Br2
D)All of the above (a-c)
E)None of the above
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7
Which fundamental step can be found in the mechanism for the following reaction? 
A)Homolysis
B)Heterolysis
C)Electrophilic elimination
D)Nucleophilic addition
E)Carbocation rearrangement

A)Homolysis
B)Heterolysis
C)Electrophilic elimination
D)Nucleophilic addition
E)Carbocation rearrangement
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8
Which of the following is true about using oxymercuration-reduction to add an OH to an alkene?
A)The mechanism is susceptible to carbocation rearrangements.
B)The mechanism proceeds through a mercurinium ion intermediate.
C)Only terminal alkenes can be used as starting materials.
D)The mechanism proceeds using anti-Markovnikov addition.
E)Reduction with NaBH4 is stereoselective.
A)The mechanism is susceptible to carbocation rearrangements.
B)The mechanism proceeds through a mercurinium ion intermediate.
C)Only terminal alkenes can be used as starting materials.
D)The mechanism proceeds using anti-Markovnikov addition.
E)Reduction with NaBH4 is stereoselective.
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9
What is the product of the following 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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10
Which of the following is true regarding carbenes?
A)They are unreactive in halogenated solvents.
B)They can be used to create epoxides.
C)They are charged species.
D)They need to be generated in situ.
E)They are highly nucleophilic.
A)They are unreactive in halogenated solvents.
B)They can be used to create epoxides.
C)They are charged species.
D)They need to be generated in situ.
E)They are highly nucleophilic.
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11
What is the product of the following reaction? 
A)I
B)II
C)III
D)IV
E)A mixture of II and III

A)I
B)II
C)III
D)IV
E)A mixture of II and III
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12
What is the product of the following 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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13
What is the product of the following 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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14
What reagent(s)will complete the following reaction? 
A)I
B)II
C)III
D)IV
E)Both III and IV will work.

A)I
B)II
C)III
D)IV
E)Both III and IV will work.
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15
When the alkene below is treated with Br2 and H2O,which is true about the stereochemistry of the product? 
A)A single enantiomer will be produced.
B)A racemic mixture will result.
C)A mixture of diastereomers will be produced.
D)A single diastereomer will be produced.
E)A meso compound will be produced.

A)A single enantiomer will be produced.
B)A racemic mixture will result.
C)A mixture of diastereomers will be produced.
D)A single diastereomer will be produced.
E)A meso compound will be produced.
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16
What is the product of the following reaction? 
A)I
B)II
C)III
D)IV
E)A mixture of III and IV

A)I
B)II
C)III
D)IV
E)A mixture of III and IV
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17
When an alkene is treated with Cl2,which of the following is not a part of the mechanism?
A)An electrophilic addition step.
B)An SN2 step.
C)The creation of a product with two anti Cl atoms.
D)A homolysis step.
E)The creation of a bromonium ion intermediate.
A)An electrophilic addition step.
B)An SN2 step.
C)The creation of a product with two anti Cl atoms.
D)A homolysis step.
E)The creation of a bromonium ion intermediate.
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18
When the alkene below is treated with Br2,which is true about the stereochemistry of the product? 
A)A pair of enantiomers will be produced.
B)A single diastereomer will be produced.
C)A mixture of diastereomers will be produced.
D)A meso compound will be produced.
E)The product will be achiral.

A)A pair of enantiomers will be produced.
B)A single diastereomer will be produced.
C)A mixture of diastereomers will be produced.
D)A meso compound will be produced.
E)The product will be achiral.
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19
What starting material is required to complete the following transformation? 
A)I
B)II
C)III
D)IV
E)Both III and IV are acceptable starting materials.

A)I
B)II
C)III
D)IV
E)Both III and IV are acceptable starting materials.
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20
What is the product of the following 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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21
Draw the detailed mechanism and the product for the following reaction. 

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22
What reagent is required to complete the following reaction? 

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23
What reagent(s)will complete the following reaction? 
A)I
B)II
C)III
D)IV
E)Both I and III will work.

A)I
B)II
C)III
D)IV
E)Both I and III will work.
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24
What is the product of the following reaction? 
A)I
B)II
C)III
D)IV
E)A mixture of III and IV

A)I
B)II
C)III
D)IV
E)A mixture of III and IV
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25
What is the product of the following reaction? 

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26
Identify the reagent(s)required to synthesize the following racemic halohydrin. 

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27
What reagent(s)will complete the following reaction? 
A)I
B)II
C)III
D)IV
E)Both I and III will work.

A)I
B)II
C)III
D)IV
E)Both I and III will work.
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28
The following alkene is treated with Br2.What is the stereochemical relationship of the two bromine atoms in the product? 

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29
What is the formal charge on a carbene?
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30
What reagent best completes the following 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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31
Which of the following reactions will produce the highest yield? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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32
What is the product of the following set of reactions? 
A)I
B)II
C)III
D)IV
E)V

A)I
B)II
C)III
D)IV
E)V
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33
What is the product of the following reaction? 
A)I
B)II
C)III
D)IV
E)A mixture of III and IV

A)I
B)II
C)III
D)IV
E)A mixture of III and IV
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34
Draw the detailed mechanism and the product for the following reaction.Be sure to include stereochemistry,if applicable. 

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35
What is the product of the following reaction? 

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36
Show how the following molecule can be synthesized from an alkene. 

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37
What is the product of the following reaction? 

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38
What is the product of the following reaction? 

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39
A carbon atom that possesses two bonds and a lone pair of electrons is called a ________.
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40
Which fundamental step does not occur in the mechanism for the reaction below? 
A)Nucleophilic addition
B)Nucleophile elimination
C)Heterolysis
D)Coordination
E)Proton transfer

A)Nucleophilic addition
B)Nucleophile elimination
C)Heterolysis
D)Coordination
E)Proton transfer
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41
Draw the product for the following reaction. 

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42
Give two ways to synthesize an epoxide starting with the given alkene.Which one is more efficient? Explain. 

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43
Draw the correct starting material for the reaction below. 

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44
What is the product of the following reaction? 

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45
Show the reagent(s)required to complete the following reaction. 

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46
Supply the three missing products. 

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47
Identify missing compounds A,B,and C. 

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48
Draw the alkene that can be epoxidized using mCPBA to yield the following compound. 

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49
Draw the product of the following reaction. 

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50
Provide the reagents needed to complete the following reaction. 

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51
What is the product of the following reaction. 

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52
What is the product of the following reaction? 

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53
Draw the products of the following reactions. 

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54
Show how the following compound can be synthesized from an alkene. 

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55
Name the reagent(s)required to complete the following reaction. 

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