Deck 6: An Overview of Organic Reactions

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Question
Identify the functional groups present in each compound below, and predict the direction of polarity in each.
Identify and predict:
amphetamine Identify the functional groups present in each compound below, and predict the direction of polarity in each. Identify and predict: amphetamine  <div style=padding-top: 35px>
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Question
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice.
Classify and explain:
azide Classify each structure below as a nucleophile or electrophile, and briefly explain your choice. Classify and explain: azide  <div style=padding-top: 35px>
Question
Polarizability:

A) explains a nonpolar carbon−sulfur bond participating in polar reaction.
B) indicates the magnitude of a dipole moment.
C) is larger for smaller atoms with few electrons.
D) is the electric field associated with a polar bond.
E) all of these
Question
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps occurs slowly due to low concentration of reactants?</strong> A)X⎯X → 2X∙ B)X∙ + R → HX + R∙ C)R∙ + X⎯X → RX + X∙ D)X∙ + R∙ → RX E)X∙ + X∙ → X⎯X F)R∙ + R∙ → R⎯R <div style=padding-top: 35px>
In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps occurs slowly due to low concentration of reactants?

A)X⎯X → 2X∙
B)X∙ + R → HX + R∙
C)R∙ + X⎯X → RX + X∙
D)X∙ + R∙ → RX
E)X∙ + X∙ → X⎯X
F)R∙ + R∙ → R⎯R
Question
Which of the following correctly compares the two elements in terms of polarizability?

A) S > O
B) F > Br
C) N > P
D) Cl > I
Question
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Indicate flow: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Indicate flow:  <div style=padding-top: 35px>
Question
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Add curved arrows to indicate electron flow in the first step.<div style=padding-top: 35px>
Refer to instructions. Add curved arrows to indicate electron flow in the first step.
Question
The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s). <strong>The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s).   Refer to instructions. If this reaction under a given set of conditions has a K<sub>eq</sub> value of 5.67, what percent conversion to the product would be expected?</strong> A) 85% B) 5.67% C) 17% D) 15% E) nearly 100% <div style=padding-top: 35px>
Refer to instructions. If this reaction under a given set of conditions has a Keq value of 5.67, what percent conversion to the product would be expected?

A) 85%
B) 5.67%
C) 17%
D) 15%
E) nearly 100%
Question
In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?

A)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d <div style=padding-top: 35px>
B)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d <div style=padding-top: 35px>
C)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d <div style=padding-top: 35px>
D)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d <div style=padding-top: 35px>
E) Both b and d
Question
Identify and label the nucleophile and electrophile in each reaction below.
Identify and label: Identify and label the nucleophile and electrophile in each reaction below. Identify and label:  <div style=padding-top: 35px>
Question
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps would be considered a chain termination step?</strong> A)X⎯X → 2X∙ B)X∙ + R → HX + R∙ C)R∙ + X⎯X → RX + X∙ D)X∙ + R∙ → RX E)X∙ + X∙ → X⎯X F)R∙ + R∙ → R⎯R <div style=padding-top: 35px>
In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps would be considered a chain termination step?

A)X⎯X → 2X∙
B)X∙ + R → HX + R∙
C)R∙ + X⎯X → RX + X∙
D)X∙ + R∙ → RX
E)X∙ + X∙ → X⎯X
F)R∙ + R∙ → R⎯R
Question
How many monochlorosubstitution products are possible for 2,3-dimethylbutane?

A) 1
B) 2
C) 4
D) 5
E) 6
Question
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice.
Classify and explain:
phenol Classify each structure below as a nucleophile or electrophile, and briefly explain your choice. Classify and explain: phenol  <div style=padding-top: 35px>
Question
In an organic reaction, which of the following is most likely to function as only a nucleophile?

A) BF3
B) (CH3)2CH2NH2
C) Fe2+
D) CH3CH2S−
E) both a and c
Question
The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s). <strong>The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s).   Refer to instructions. The forward and reverse reactions are classified, respectively, as:</strong> A) addition, elimination B) elimination, substitution C) elimination, addition D) elimination, rearrangement E) substitution, addition <div style=padding-top: 35px>
Refer to instructions. The forward and reverse reactions are classified, respectively, as:

A) addition, elimination
B) elimination, substitution
C) elimination, addition
D) elimination, rearrangement
E) substitution, addition
Question
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Species B is:</strong> A) a carbocation B) a radical C) a carbanion D) a free radical <div style=padding-top: 35px>
Refer to instructions. Species B is:

A) a carbocation
B) a radical
C) a carbanion
D) a free radical
Question
Consider the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Consider the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. This reaction is an example of:</strong> A) a substitution reaction. B) a rearrangement reaction. C) an elimination reaction. D) an addition reaction. <div style=padding-top: 35px>
Refer to instructions. This reaction is an example of:

A) a substitution reaction.
B) a rearrangement reaction.
C) an elimination reaction.
D) an addition reaction.
Question
Which of the following is a characteristic of a polar reaction?

A) symmetrical bond making and breaking
B) one electron from each reactant forms the bond
C) involves a neutral species with an unpaired electron
D) are more common that radical reactions
E) all of these
Question
Identify the functional groups present in each compound below, and predict the direction of polarity in each.
Identify and predict:
mustard gas Cl−CH2CH2−S−CH2CH2−Cl
Question
Identify and label the nucleophile and electrophile in each reaction below.
Identify and label: Identify and label the nucleophile and electrophile in each reaction below. Identify and label:  <div style=padding-top: 35px>
Question
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
The structures below show the stepwise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step. Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. The structures below show the stepwise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step.  <div style=padding-top: 35px>
Question
Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Draw arrows on the structures above showing electron flow in steps two and three of this reaction.<div style=padding-top: 35px>
Refer to instructions. Draw arrows on the structures above showing electron flow in steps two and three of this reaction.
Question
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Indicate flow: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Indicate flow:  <div style=padding-top: 35px>
Question
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The transition state is found at _____ on the diagram.</strong> A)A B)B C)C D)D <div style=padding-top: 35px>
The transition state is found at _____ on the diagram.

A)A
B)B
C)C
D)D
Question
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Label and indicate flow: In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Label and indicate flow:  <div style=padding-top: 35px>
Question
Match each definition to one of the terms below.
The energy needed by reactants to reach the transition state.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
Question
Match each definition to one of the terms below.
Another term used for a Lewis acid.

A)polarization
B)addition reaction
C)radical reaction
D)electrophile
E)polar reaction
F)substitution
G)nucleophile
H)elimination reaction
Question
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The free-energy change for the reaction is indicated at _____ on the diagram.</strong> A)A B)B C)C D)D <div style=padding-top: 35px>
The free-energy change for the reaction is indicated at _____ on the diagram.

A)A
B)B
C)C
D)D
Question
Match each definition to one of the terms below.
ΔG° = −RT ln Keq

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
Question
Match each definition to one of the terms below.
A reaction where ΔG° is positive.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
Question
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
If the yield for the following reaction is 76%, calculate Keq and predict the sign of ΔG°. Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. If the yield for the following reaction is 76%, calculate K<sub>eq</sub> and predict the sign of ΔG°.  <div style=padding-top: 35px>
Question
Match each definition to one of the terms below.
A reaction that involves a species with an unpaired electron.

A)polarization
B)addition reaction
C)radical reaction
D)electrophile
E)polar reaction
F)substitution
G)nucleophile
H)elimination reaction
Question
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Predict the two alcohol addition products obtained by reaction of the following alkene with aqueous acid. In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Predict the two alcohol addition products obtained by reaction of the following alkene with aqueous acid.  <div style=padding-top: 35px>
Question
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Predict the product of the following reaction of Prostaglandin H2 by interpreting the flow of electrons as indicated by the curved arrows. In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Predict the product of the following reaction of Prostaglandin H<sub>2</sub> by interpreting the flow of electrons as indicated by the curved arrows.  <div style=padding-top: 35px>
Question
Match each definition to one of the terms below.
A species that lies at an energy maximum during an individual step in a reaction.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
Question
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The products are found at _____ on the diagram.</strong> A)A B)B C)C D)D <div style=padding-top: 35px>
The products are found at _____ on the diagram.

A)A
B)B
C)C
D)D
Question
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Consider the following reaction: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Consider the following reaction:   a)Assuming that the first step is the slow step, draw and label a qualitative energy diagram for the reaction. b)If the second step of the reaction were the slow step, briefly explain how the values of ΔG<sup>‡</sup><sub>1</sub>, ΔG<sup>‡</sup><sub>2</sub>, and ΔG° would change.<div style=padding-top: 35px> a)Assuming that the first step is the slow step, draw and label a qualitative energy diagram for the reaction.
b)If the second step of the reaction were the slow step, briefly explain how the values of ΔG1, ΔG2, and ΔG° would change.
Question
Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Label the nucleophile, Nu, and the electrophile, E<sup>+</sup>, in the blanks provided under the structures.<div style=padding-top: 35px>
Refer to instructions. Label the nucleophile, Nu, and the electrophile, E+, in the blanks provided under the structures.
Question
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The reactants are found at _____ on the diagram.</strong> A)A B)B C)C D)D <div style=padding-top: 35px>
The reactants are found at _____ on the diagram.

A)A
B)B
C)C
D)D
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Deck 6: An Overview of Organic Reactions
1
Identify the functional groups present in each compound below, and predict the direction of polarity in each.
Identify and predict:
amphetamine Identify the functional groups present in each compound below, and predict the direction of polarity in each. Identify and predict: amphetamine
2
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice.
Classify and explain:
azide Classify each structure below as a nucleophile or electrophile, and briefly explain your choice. Classify and explain: azide
Azide ion is a nucleophile because it has a net negative charge (and lots of nonbonding electron electron pairs!).
3
Polarizability:

A) explains a nonpolar carbon−sulfur bond participating in polar reaction.
B) indicates the magnitude of a dipole moment.
C) is larger for smaller atoms with few electrons.
D) is the electric field associated with a polar bond.
E) all of these
explains a nonpolar carbon−sulfur bond participating in polar reaction.
4
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps occurs slowly due to low concentration of reactants?</strong> A)X⎯X → 2X∙ B)X∙ + R → HX + R∙ C)R∙ + X⎯X → RX + X∙ D)X∙ + R∙ → RX E)X∙ + X∙ → X⎯X F)R∙ + R∙ → R⎯R
In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps occurs slowly due to low concentration of reactants?

A)X⎯X → 2X∙
B)X∙ + R → HX + R∙
C)R∙ + X⎯X → RX + X∙
D)X∙ + R∙ → RX
E)X∙ + X∙ → X⎯X
F)R∙ + R∙ → R⎯R
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5
Which of the following correctly compares the two elements in terms of polarizability?

A) S > O
B) F > Br
C) N > P
D) Cl > I
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6
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Indicate flow: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Indicate flow:
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7
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Add curved arrows to indicate electron flow in the first step.
Refer to instructions. Add curved arrows to indicate electron flow in the first step.
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8
The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s). <strong>The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s).   Refer to instructions. If this reaction under a given set of conditions has a K<sub>eq</sub> value of 5.67, what percent conversion to the product would be expected?</strong> A) 85% B) 5.67% C) 17% D) 15% E) nearly 100%
Refer to instructions. If this reaction under a given set of conditions has a Keq value of 5.67, what percent conversion to the product would be expected?

A) 85%
B) 5.67%
C) 17%
D) 15%
E) nearly 100%
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9
In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?

A)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d
B)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d
C)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d
D)
<strong>In theory, upon reaction with water in the presence of a strong acid, which of the following will produce more than one isomeric product?</strong> A)   B)   C)   D)   E) Both b and d
E) Both b and d
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10
Identify and label the nucleophile and electrophile in each reaction below.
Identify and label: Identify and label the nucleophile and electrophile in each reaction below. Identify and label:
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11
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps would be considered a chain termination step?</strong> A)X⎯X → 2X∙ B)X∙ + R → HX + R∙ C)R∙ + X⎯X → RX + X∙ D)X∙ + R∙ → RX E)X∙ + X∙ → X⎯X F)R∙ + R∙ → R⎯R
In the following generic reaction between a halogen (X) and an alkane (R), which of the following steps would be considered a chain termination step?

A)X⎯X → 2X∙
B)X∙ + R → HX + R∙
C)R∙ + X⎯X → RX + X∙
D)X∙ + R∙ → RX
E)X∙ + X∙ → X⎯X
F)R∙ + R∙ → R⎯R
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12
How many monochlorosubstitution products are possible for 2,3-dimethylbutane?

A) 1
B) 2
C) 4
D) 5
E) 6
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13
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice.
Classify and explain:
phenol Classify each structure below as a nucleophile or electrophile, and briefly explain your choice. Classify and explain: phenol
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14
In an organic reaction, which of the following is most likely to function as only a nucleophile?

A) BF3
B) (CH3)2CH2NH2
C) Fe2+
D) CH3CH2S−
E) both a and c
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15
The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s). <strong>The reaction below is commonly used as a laboratory preparation of cyclohexene. Use this reaction to answer the following question(s).   Refer to instructions. The forward and reverse reactions are classified, respectively, as:</strong> A) addition, elimination B) elimination, substitution C) elimination, addition D) elimination, rearrangement E) substitution, addition
Refer to instructions. The forward and reverse reactions are classified, respectively, as:

A) addition, elimination
B) elimination, substitution
C) elimination, addition
D) elimination, rearrangement
E) substitution, addition
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16
Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Use the first step of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Species B is:</strong> A) a carbocation B) a radical C) a carbanion D) a free radical
Refer to instructions. Species B is:

A) a carbocation
B) a radical
C) a carbanion
D) a free radical
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17
Consider the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). <strong>Consider the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. This reaction is an example of:</strong> A) a substitution reaction. B) a rearrangement reaction. C) an elimination reaction. D) an addition reaction.
Refer to instructions. This reaction is an example of:

A) a substitution reaction.
B) a rearrangement reaction.
C) an elimination reaction.
D) an addition reaction.
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18
Which of the following is a characteristic of a polar reaction?

A) symmetrical bond making and breaking
B) one electron from each reactant forms the bond
C) involves a neutral species with an unpaired electron
D) are more common that radical reactions
E) all of these
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19
Identify the functional groups present in each compound below, and predict the direction of polarity in each.
Identify and predict:
mustard gas Cl−CH2CH2−S−CH2CH2−Cl
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20
Identify and label the nucleophile and electrophile in each reaction below.
Identify and label: Identify and label the nucleophile and electrophile in each reaction below. Identify and label:
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21
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
The structures below show the stepwise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step. Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. The structures below show the stepwise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step.
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22
Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Draw arrows on the structures above showing electron flow in steps two and three of this reaction.
Refer to instructions. Draw arrows on the structures above showing electron flow in steps two and three of this reaction.
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23
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Indicate flow: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Indicate flow:
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24
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The transition state is found at _____ on the diagram.</strong> A)A B)B C)C D)D
The transition state is found at _____ on the diagram.

A)A
B)B
C)C
D)D
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25
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Label and indicate flow: In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Label and indicate flow:
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26
Match each definition to one of the terms below.
The energy needed by reactants to reach the transition state.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
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27
Match each definition to one of the terms below.
Another term used for a Lewis acid.

A)polarization
B)addition reaction
C)radical reaction
D)electrophile
E)polar reaction
F)substitution
G)nucleophile
H)elimination reaction
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28
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The free-energy change for the reaction is indicated at _____ on the diagram.</strong> A)A B)B C)C D)D
The free-energy change for the reaction is indicated at _____ on the diagram.

A)A
B)B
C)C
D)D
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29
Match each definition to one of the terms below.
ΔG° = −RT ln Keq

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
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30
Match each definition to one of the terms below.
A reaction where ΔG° is positive.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
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31
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
If the yield for the following reaction is 76%, calculate Keq and predict the sign of ΔG°. Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. If the yield for the following reaction is 76%, calculate K<sub>eq</sub> and predict the sign of ΔG°.
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32
Match each definition to one of the terms below.
A reaction that involves a species with an unpaired electron.

A)polarization
B)addition reaction
C)radical reaction
D)electrophile
E)polar reaction
F)substitution
G)nucleophile
H)elimination reaction
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33
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Predict the two alcohol addition products obtained by reaction of the following alkene with aqueous acid. In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Predict the two alcohol addition products obtained by reaction of the following alkene with aqueous acid.
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34
In the reaction below:
a)Label the nucleophile (Nu) and the electrophile (E).
b)Draw arrows on the structures showing electron flow in the reaction.
Predict the product of the following reaction of Prostaglandin H2 by interpreting the flow of electrons as indicated by the curved arrows. In the reaction below: a)Label the nucleophile (Nu) and the electrophile (E). b)Draw arrows on the structures showing electron flow in the reaction. Predict the product of the following reaction of Prostaglandin H<sub>2</sub> by interpreting the flow of electrons as indicated by the curved arrows.
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35
Match each definition to one of the terms below.
A species that lies at an energy maximum during an individual step in a reaction.

A)transition state
B)endergonic reaction
C)activation energy
D)Gibbs free energy change
E)exergonic reaction
F)reaction intermediate
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36
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The products are found at _____ on the diagram.</strong> A)A B)B C)C D)D
The products are found at _____ on the diagram.

A)A
B)B
C)C
D)D
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37
Add curved arrows to the following reaction(s) to indicate the flow of electrons in each.
Consider the following reaction: Add curved arrows to the following reaction(s) to indicate the flow of electrons in each. Consider the following reaction:   a)Assuming that the first step is the slow step, draw and label a qualitative energy diagram for the reaction. b)If the second step of the reaction were the slow step, briefly explain how the values of ΔG<sup>‡</sup><sub>1</sub>, ΔG<sup>‡</sup><sub>2</sub>, and ΔG° would change. a)Assuming that the first step is the slow step, draw and label a qualitative energy diagram for the reaction.
b)If the second step of the reaction were the slow step, briefly explain how the values of ΔG1, ΔG2, and ΔG° would change.
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38
Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s). Use the second and third steps of the reaction of 2-bromo-2-methylpropane with water, shown below, to answer the following question(s).   Refer to instructions. Label the nucleophile, Nu, and the electrophile, E<sup>+</sup>, in the blanks provided under the structures.
Refer to instructions. Label the nucleophile, Nu, and the electrophile, E+, in the blanks provided under the structures.
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39
Use the reaction energy diagram below to answer the following question(s). <strong>Use the reaction energy diagram below to answer the following question(s).   The reactants are found at _____ on the diagram.</strong> A)A B)B C)C D)D
The reactants are found at _____ on the diagram.

A)A
B)B
C)C
D)D
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Unlock Deck
Unlock for access to all 39 flashcards in this deck.