Deck 10: Radical Reactions

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Question
For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH3)2CH-H CH3CH2CH2-H H-F
(413 kJ mol-1) (423 kJ mol-1) (570 kJ mol-1)
H-Cl H-Br
(432 kJ mol-1) (366 kJ mol-1)

A)
 <strong>For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH<sub>3</sub>)<sub>2</sub>CH-H CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>-H H-F (413 kJ mol<sup>-1</sup>) (423 kJ mol<sup>-1</sup>) (570 kJ mol<sup>-1</sup>) H-Cl H-Br (432 kJ mol<sup>-1</sup>) (366 kJ mol<sup>-1</sup>)</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + F·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HF C)   D) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HCl E) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Br·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HBr <div style=padding-top: 35px>
B) CH3CH2CH3 + F· \rightarrow CH3CH2CH2· + HF
C)
 <strong>For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH<sub>3</sub>)<sub>2</sub>CH-H CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>-H H-F (413 kJ mol<sup>-1</sup>) (423 kJ mol<sup>-1</sup>) (570 kJ mol<sup>-1</sup>) H-Cl H-Br (432 kJ mol<sup>-1</sup>) (366 kJ mol<sup>-1</sup>)</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + F·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HF C)   D) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HCl E) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Br·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HBr <div style=padding-top: 35px>
D) CH3CH2CH3 + Cl· \rightarrow CH3CH2CH2· + HCl
E) CH3CH2CH3 + Br· \rightarrow CH3CH2CH2· + HBr
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Question
Which of the reactions listed below would be exothermic?

A) CH3-CH3 \rightarrow 2CH3·
B) CH3· + CH4 \rightarrow CH4 + CH3·
C) 2(CH3)2CH· \rightarrow (CH3)2CH-CH(CH3)2
D) H· + (CH3)3CH \rightarrow (CH3)3CH + H·
E) None of the above
Question
How many different monochlorobutanes (including stereoisomers)are formed in the free radical chlorination of butane?

A) 1
B) 2
C) 3
D) 4
E) 5
Question
A chain reaction is one that:

A) involves a series of steps.
B) involves two steps of equal activation energy.
C) is one that can be initiated by light.
D) involves a series of steps,each of which generates a reactive intermediate that brings about the next step.
E) involves free radicals that have an unusual stability and thereby cause a large quantum yield.
Question
Which of the reactions listed below would have a value of Δ\Delta H° equal to zero?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3-H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) Reactions (B)and (D)
Question
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall \Delta H° for the reaction.  </strong> A) +437 kJ / mol B) -437 kJ / mol C) -411 kJ / mol D) +26 kJ / mol E) -1581 kJ / mol<sup> </sup> <div style=padding-top: 35px>

A) +437 kJ / mol
B) -437 kJ / mol
C) -411 kJ / mol
D) +26 kJ / mol
E) -1581 kJ / mol
Question
Which of the following free radicals is the most stable?

A)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of these molecules is not expected to arise as a product of the high temperature chlorination of methane?

A) CCl4
B) HCCl3
C) CH2Cl2
D) CH3CH3
E) CH2=CH2
Question
The reaction of Cl2 with a methyl radical has a positive Δ\Delta H°.Which of these drawings is the best representation of the transition state of this reaction?

A)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) +243 kJ / mol B) -138 kJ / mol C) +138 kJ / mol D) -781 kJ / mol E) +781 kJ / mol <div style=padding-top: 35px>

A) +243 kJ / mol
B) -138 kJ / mol
C) +138 kJ / mol
D) -781 kJ / mol
E) +781 kJ / mol
Question
If chlorocyclopentane were chlorinated to form all possible dichloro compounds and the product mixture subjected to precise fractional distillation,how many fractions would be obtained (ideally)?

A) 3
B) 4
C) 5
D) 7
E) 9
Question
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) -121 kJ / mol B) +121 kJ / mol C) +243 kJ / mol D) +664 kJ / mol E) -785 kJ / mol <div style=padding-top: 35px>

A) -121 kJ / mol
B) +121 kJ / mol
C) +243 kJ / mol
D) +664 kJ / mol
E) -785 kJ / mol
Question
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) +616 kJ / mol B) -101 kJ / mol C) -173 kJ / mol D) +57 kJ kJ / mol E) -44 kJ / mol <div style=padding-top: 35px>

A) +616 kJ / mol
B) -101 kJ / mol
C) -173 kJ / mol
D) +57 kJ kJ / mol
E) -44 kJ / mol
Question
Which of the following gas-phase reactions is a possible chain-terminating step in the light-initiated chlorination of methane?

A) Cl-Cl \rightarrow 2Cl·
B) Cl· + CH4 \rightarrow CH3· + H-Cl
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + Cl-Cl \rightarrow CH3Cl + Cl·
E) More than one of the above
Question
Which of the reactions listed below would be exothermic?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3-H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) All of the above
Question
The reaction of 2-methylbutane with chlorine would yield how many monochloro derivatives? (include stereoisomers)

A) 2
B) 3
C) 4
D) 5
E) 6
Question
In the presence of light,ethane (1 mol)reacts with chlorine (1 mol)to form which product(s)?

A) CH2ClCHCl2
B) CH3CHCl2
C) CH3CH2Cl
D) ClCH2CH2Cl
E) All of these
Question
The Δ\Delta H° value is expected to be least for which indicated C-H bond of isopentane?

A)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Hydrogen atom abstraction from which position would yield the most stable free radical intermediate during the reaction of bromine with 2,2,3-trimethylpentane?

A) C1
B) C2
C) C3
D) C4
E) C5
Question
An alternate mechanism for the chlorination of methane is: Cl2 \rightarrow 2Cl·
Cl-Cl, Δ\Delta H° = 243 kJ mol-1
Cl· + CH4 \rightarrow CH3Cl + H·
CH3-H, Δ\Delta H° = 440 kJ mol-1
H· + Cl2 \rightarrow HCl + Cl·
CH3-Cl, Δ\Delta H° = 352 kJ mol-1
H-Cl, Δ\Delta H° = 432 kJ mol -1
This mechanism is unlikely because:

A) The overall Δ\Delta H° is highly endothermic.
B) The probability factor is low.
C) One of the chain propagating steps is non-productive.
D) One of the chain propagating steps has a very high Eact.
E) One of the chain propagating steps is highly exothermic.
Question
In the presence of light at 25°C,isobutane (1 mol)and bromine (1 mol)yield which monobromo product(s)?

A) 2-Methyl-1-bromopropane (almost exclusively)
B) 2-Methyl-2-bromopropane (almost exclusively)
C) A mixture of 50% (A)and 50% (B)
D) A mixture of 90% (A)and 10% (B)
E) Butyl bromide
Question
Which of the following reactions would have an activation energy equal to zero?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3--H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) All of the above
Question
Which of the following reactions would have the smallest energy of activation?

A)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following statements is true when used to compare the reaction of fluorine with 2-methylhexane and the reaction of bromine with 2-methylhexane?

A) Bromine is the less reactive and the less selective,giving 2-bromo-2-methyl hexane as one of several products.
B) Fluorine is the less reactive and the more selective,giving 2-fluoro-2-methyl hexane as the major product.
C) Fluorine is the more reactive and less selective,giving 2-fluoro-2-methyl hexane as one of several products.
D) Bromine is the more reactive and the more selective,giving 2-bromo-2-methyl hexane as the major product.
E) More than one of the above statements is true.
Question
For which of the following gas-phase reactions would the Eact be equal to Δ\Delta H°?

A) Cl-Cl \rightarrow 2Cl·
B) 2 Cl· \rightarrow Cl-Cl
C) Cl· + CH4 \rightarrow CH3· + H-Cl
D) CH3· + CH3· \rightarrow CH3-CH3
E) CH3· + Cl-Cl \rightarrow CH3-Cl + Cl·
Question
Which of the following reactions would have an activation energy equal to zero?

A) CH3-CH3 -- \rightarrow 2CH3·
B) H· + CH3CH3 -- \rightarrow CH3CH3 + H·
C) 2CH3CH2· -- \rightarrow CH3CH2CH2CH3
D) CH3· + CH3CH3 -- \rightarrow CH3CH3 + CH3·
E) None of the above
Question
Select the structure of the major product formed in the following reaction. <strong>Select the structure of the major product formed in the following reaction.  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What feature would you expect to see in the 1H NMR spectrum of B after subjecting A to the following reaction? <strong>What feature would you expect to see in the <sup>1</sup>H NMR spectrum of B after subjecting A to the following reaction?  </strong> A) There would be only 4 aromatic protons at low field. B) The signal for the protons on the benzylic carbon would be a doublet. C) The signal for the methyl protons would be a triplet. D) The signal for the methyl protons would be a doublet. E) The signal for the methyl protons would integrate for only 2 hydrogens. <div style=padding-top: 35px>

A) There would be only 4 aromatic protons at low field.
B) The signal for the protons on the benzylic carbon would be a doublet.
C) The signal for the methyl protons would be a triplet.
D) The signal for the methyl protons would be a doublet.
E) The signal for the methyl protons would integrate for only 2 hydrogens.
Question
At some temperatures,the relative reactivities of 3°,2° and 1° alkane hydrogens in free radical chlorination are in the ratio of 5:3:1.Thus,monochlorination of isopentane should produce these percentages of 2-chloro-2-methylbutane (A),combined 1-chloro-2-methylbutane and 1-chloro-3-methylbutane (B),and 2-chloro-3-methylbutane (C):

A) 8% A,75% B,17% C
B) 25% A,45% B,30% C
C) 29% A,44% B,18% C
D) 30% A,35% B,35% C
E) 36% A,43% B,21% C
Question
Which reaction would you expect to have the smallest energy of activation? Δ\Delta H°(kJ mol-1)

A) CH3· + CH3· -- \rightarrow CH3CH3 -378
B) CH4 + F· -- \rightarrow CH3· + HF -130
C) CH4 + I· -- \rightarrow CH3· + HI +142
D) CH4 + Br· -- \rightarrow CH3· + HBr +104
E) CH4 + Cl· -- \rightarrow CH3· + HCl +8
Question
An example of a reaction having an Eact = 0 would be:

A) Br· + Br-Br -- \rightarrow Br-Br + Br·
B) F· + CH4 -- \rightarrow H-F + CH3·
C) CH3· + Cl· -- \rightarrow CH3Cl
D) More than one of these
E) None of these
Question
What sequence of reactions could be used to prepare cis-1,2-cyclopentanediol from cyclopentane?

A) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)OsO4; (4)NaHSO3/H2O
B) (1)t-BuOK/t-BuOH; (2)Cl2,h ν\nu ; (3)NaOH/H2O
C) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)H2O2
D) (1)NaOH/H2O; (2)Br2; (3)NaNH2(2eq. )/liq.NH3; (4)KMnO4,NaOH/H2O,5°C
E) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)Hg(OAc)2,H2O (4)NaBH4,H3O+
Question
Which of the following reactions would have the smallest energy of activation?

A) CH4 + Br· \rightarrow CH3· + HBr
B) CH3CH3 + Br· \rightarrow CH3CH2· + HBr
C)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
D)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
E)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
Question
An example of a reaction having an Eact = 0 would be:

A) Br· + Br-Br \rightarrow Br-Br + Br·
B) F· + CH4 \rightarrow H-F + CH3·
C) CH3· + CH3CH3 \rightarrow CH4 + CH3CH2·
D) Br· + H-Br \rightarrow H-Br + Br·
E) CH3· + CH3· \rightarrow CH3-CH3
Question
Which reaction would you expect to have the largest energy of activation? Δ\Delta H° (kJ mol-1)

A) CH3· + CH3· \rightarrow CH3CH3 -378
B) CH3· + Br· \rightarrow CH3Br -130
C) CH4 + I· \rightarrow CH3· + HI +142
D) CH4 + Br· \rightarrow CH3· + HBr +104
E) CH4 + Cl· \rightarrow CH3· + HCl +8
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which of the following reactions should have the smallest energy of activation?

A) CH4 + Cl· \rightarrow CH3· + HCl
B) CH3CH3 + Cl· \rightarrow CH3CH2· + HCl
C)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)   <div style=padding-top: 35px>
D)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)   <div style=padding-top: 35px>
E)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)   <div style=padding-top: 35px>
Question
When an alkane in which all hydrogen atoms are not equivalent is monosubstituted,use of this halogen produces a ratio of isomers which is essentially statistical,i.e. ,dependent only on the number of each type of hydrogen.

A) F2
B) Cl2
C) Br2
D) I2
E) All of the above
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which is true for a chain-terminating step?

A) "A new free radical is formed."
B) "The process is endothermic."
C) "Eact = 0."
D) " Δ\Delta H° is positive."
E) "A product is formed which is immune to further reaction."
Question
For which reaction would the transition state be most product-like?

A) CH4 + Br· \rightarrow CH3· + HBr
B) CH3CH3 + Br· \rightarrow CH3CH2· + HBr
C)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
D)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
E)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)   <div style=padding-top: 35px>
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He <div style=padding-top: 35px>

A) Ha
B) Hb
C) Hc
D) Hd
E) He
Question
Free radical mono-halogenation of an alkane is typically conducted using bromine versus chlorine because

A) the bromine radical is more reactive and therefore more selective.
B) the chlorine radical is more reactive and therefore more selective.
C) the chlorine radical is less reactive and therefore more selective.
D) the bromine radical is less reactive and therefore more selective.
E) None of the above
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He <div style=padding-top: 35px>

A) Ha
B) Hb
C) Hc
D) Hd
E) He
Question
What is the final product,C,obtained via the following reaction sequence? <strong>What is the final product,C,obtained via the following reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He <div style=padding-top: 35px>

A) Ha
B) Hb
C) Hc
D) Hd
E) He
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following reaction sequence? <strong>What is the product for the following reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He <div style=padding-top: 35px>

A) Ha
B) Hb
C) Hc
D) Hd
E) He
Question
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px> , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He <div style=padding-top: 35px>

A) Ha
B) Hb
C) Hc
D) Hd
E) He
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
The free radical chlorination of pentane produces this number of monochloro compounds,including stereoisomers.

A) 2
B) 3
C) 4
D) 5
E) 6
Question
The free radical chlorination of 3-chloropentane forms a mixture of dichloropentanes which,on precise fractional distillation,affords these fractions:

A) 4 fractions,none optically active
B) 4 fractions,2 optically active
C) 7 fractions,4 optically active
D) 7 fractions,6 optically active
E) 7 fractions,all optically active
Question
More than one monochloro compound can be obtained from the free radical chlorination of:

A) Cyclopentane
B) Neopentane
C) Isobutane
D) Ethane
E) Methane
Question
The p-orbital of a methyl radical carbon,CH3·,contains how many electrons?

A) 1
B) 2
C) 3
D) 4
E) 0
Question
What product would result from the following reaction? <strong>What product would result from the following reaction?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the total number of trichloropropanes which can be produced by free radical chlorination of propane? Include all stereoisomers.

A) 4
B) 5
C) 6
D) 7
E) 8
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Free radical chlorination of hexane produces this number of monochloro derivatives (including stereoisomers):

A) 3
B) 4
C) 5
D) 7
E) 8
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
How many monochloro derivatives,including stereoisomers,can be formed in the chlorination of 1-bromobutane?

A) 4
B) 5
C) 6
D) 7
E) 8
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
The reaction of 1-butene with HBr in the presence of peroxides yields 1-bromobutane.The mechanism for the reaction involves:

A) attack on the alkene by a Br+ ion.
B) attack on the alkene by a H+ ion.
C) attack on the alkene by a bromine atom,Br·.
D) attack on the alkene by a hydrogen atom,H·.
E) isomerization of the 2-bromobutane produced initially.
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V <div style=padding-top: 35px>

A) I
B) II
C) III
D) IV
E) V
Question
Which of the following would serve as the best synthesis of 2-bromohexane?

A)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable. <div style=padding-top: 35px>
B)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable. <div style=padding-top: 35px>
C)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable. <div style=padding-top: 35px>
D)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable. <div style=padding-top: 35px>
E) All of the above would be equally suitable.
Question
The free radical chlorination of (R)-2-chloropentane forms a mixture of dichloropentanes which includes:

A) three optically active compounds.
B) two achiral compounds.
C) two meso compounds.
D) one pair of diastereomers.
E) one racemic mixture.
Question
Consider the light-initiated chlorination of (S)-2-chlorobutane followed by careful fractional distillation (or separation by GLC)of all of the products with the formula C4H8Cl2.How many fractions (in total)would be obtained and how many of these fractions would be optically active?

A) Three fractions total;all optically active
B) Four fractions total;three fractions optically active
C) Five fractions total;all optically active
D) Five fractions total;four fractions optically active
E) Five fractions total;three fractions optically active
Question
Free radical chlorination will produce but one monochloro derivative in the case of:

A) Propane
B) Butane
C) Isobutane
D) Isopentane
E) Neopentane
Question
Which of the following combinations of reactants can provide a demonstrable example of anti-Markovnikov addition?

A) CH2=CHCH3 + HCl + ROOR
B) CH3CH=CH2 + H2O + Cl2
C) CH3CH=CHCH3 + HBr + ROOR
D) CH3CH2CH=CH2 + HBr + ROOR
E) CH3CH2CH=CH2 + Br2 + ROOR
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Deck 10: Radical Reactions
1
For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH3)2CH-H CH3CH2CH2-H H-F
(413 kJ mol-1) (423 kJ mol-1) (570 kJ mol-1)
H-Cl H-Br
(432 kJ mol-1) (366 kJ mol-1)

A)
 <strong>For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH<sub>3</sub>)<sub>2</sub>CH-H CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>-H H-F (413 kJ mol<sup>-1</sup>) (423 kJ mol<sup>-1</sup>) (570 kJ mol<sup>-1</sup>) H-Cl H-Br (432 kJ mol<sup>-1</sup>) (366 kJ mol<sup>-1</sup>)</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + F·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HF C)   D) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HCl E) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Br·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HBr
B) CH3CH2CH3 + F· \rightarrow CH3CH2CH2· + HF
C)
 <strong>For which of the following reactions would the transition state most resemble the products? The following bond dissociation energies may be useful. (CH<sub>3</sub>)<sub>2</sub>CH-H CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>-H H-F (413 kJ mol<sup>-1</sup>) (423 kJ mol<sup>-1</sup>) (570 kJ mol<sup>-1</sup>) H-Cl H-Br (432 kJ mol<sup>-1</sup>) (366 kJ mol<sup>-1</sup>)</strong> A)   B) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + F·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HF C)   D) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HCl E) CH<sub>3</sub>CH<sub>2</sub>CH<sub>3</sub> + Br·  \rightarrow CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>· + HBr
D) CH3CH2CH3 + Cl· \rightarrow CH3CH2CH2· + HCl
E) CH3CH2CH3 + Br· \rightarrow CH3CH2CH2· + HBr
CH3CH2CH3 + Br· \rightarrow CH3CH2CH2· + HBr
2
Which of the reactions listed below would be exothermic?

A) CH3-CH3 \rightarrow 2CH3·
B) CH3· + CH4 \rightarrow CH4 + CH3·
C) 2(CH3)2CH· \rightarrow (CH3)2CH-CH(CH3)2
D) H· + (CH3)3CH \rightarrow (CH3)3CH + H·
E) None of the above
2(CH3)2CH· \rightarrow (CH3)2CH-CH(CH3)2
3
How many different monochlorobutanes (including stereoisomers)are formed in the free radical chlorination of butane?

A) 1
B) 2
C) 3
D) 4
E) 5
3
4
A chain reaction is one that:

A) involves a series of steps.
B) involves two steps of equal activation energy.
C) is one that can be initiated by light.
D) involves a series of steps,each of which generates a reactive intermediate that brings about the next step.
E) involves free radicals that have an unusual stability and thereby cause a large quantum yield.
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5
Which of the reactions listed below would have a value of Δ\Delta H° equal to zero?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3-H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) Reactions (B)and (D)
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6
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall \Delta H° for the reaction.  </strong> A) +437 kJ / mol B) -437 kJ / mol C) -411 kJ / mol D) +26 kJ / mol E) -1581 kJ / mol<sup> </sup>

A) +437 kJ / mol
B) -437 kJ / mol
C) -411 kJ / mol
D) +26 kJ / mol
E) -1581 kJ / mol
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7
Which of the following free radicals is the most stable?

A)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following free radicals is the most stable?</strong> A)   B)   C)   D)   E)
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8
Which of these molecules is not expected to arise as a product of the high temperature chlorination of methane?

A) CCl4
B) HCCl3
C) CH2Cl2
D) CH3CH3
E) CH2=CH2
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9
The reaction of Cl2 with a methyl radical has a positive Δ\Delta H°.Which of these drawings is the best representation of the transition state of this reaction?

A)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)
B)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)
C)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)
D)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)
E)
 <strong>The reaction of Cl<sub>2</sub> with a methyl radical has a positive  \Delta H°.Which of these drawings is the best representation of the transition state of this reaction?</strong> A)   B)   C)   D)   E)
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10
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) +243 kJ / mol B) -138 kJ / mol C) +138 kJ / mol D) -781 kJ / mol E) +781 kJ / mol

A) +243 kJ / mol
B) -138 kJ / mol
C) +138 kJ / mol
D) -781 kJ / mol
E) +781 kJ / mol
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11
If chlorocyclopentane were chlorinated to form all possible dichloro compounds and the product mixture subjected to precise fractional distillation,how many fractions would be obtained (ideally)?

A) 3
B) 4
C) 5
D) 7
E) 9
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12
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) -121 kJ / mol B) +121 kJ / mol C) +243 kJ / mol D) +664 kJ / mol E) -785 kJ / mol

A) -121 kJ / mol
B) +121 kJ / mol
C) +243 kJ / mol
D) +664 kJ / mol
E) -785 kJ / mol
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13
The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall Δ\Delta H° for the reaction.  <strong>The bond dissociation energies for the relevant bonds are given below each of the species involved in the following reaction.Calculate the overall  \Delta H° for the reaction.  </strong> A) +616 kJ / mol B) -101 kJ / mol C) -173 kJ / mol D) +57 kJ kJ / mol E) -44 kJ / mol

A) +616 kJ / mol
B) -101 kJ / mol
C) -173 kJ / mol
D) +57 kJ kJ / mol
E) -44 kJ / mol
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14
Which of the following gas-phase reactions is a possible chain-terminating step in the light-initiated chlorination of methane?

A) Cl-Cl \rightarrow 2Cl·
B) Cl· + CH4 \rightarrow CH3· + H-Cl
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + Cl-Cl \rightarrow CH3Cl + Cl·
E) More than one of the above
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15
Which of the reactions listed below would be exothermic?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3-H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) All of the above
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16
The reaction of 2-methylbutane with chlorine would yield how many monochloro derivatives? (include stereoisomers)

A) 2
B) 3
C) 4
D) 5
E) 6
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17
In the presence of light,ethane (1 mol)reacts with chlorine (1 mol)to form which product(s)?

A) CH2ClCHCl2
B) CH3CHCl2
C) CH3CH2Cl
D) ClCH2CH2Cl
E) All of these
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18
The Δ\Delta H° value is expected to be least for which indicated C-H bond of isopentane?

A)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)
B)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)
C)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)
D)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)
E)
 <strong>The  \Delta H° value is expected to be least for which indicated C-H bond of isopentane?</strong> A)   B)   C)   D)   E)
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19
Hydrogen atom abstraction from which position would yield the most stable free radical intermediate during the reaction of bromine with 2,2,3-trimethylpentane?

A) C1
B) C2
C) C3
D) C4
E) C5
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20
An alternate mechanism for the chlorination of methane is: Cl2 \rightarrow 2Cl·
Cl-Cl, Δ\Delta H° = 243 kJ mol-1
Cl· + CH4 \rightarrow CH3Cl + H·
CH3-H, Δ\Delta H° = 440 kJ mol-1
H· + Cl2 \rightarrow HCl + Cl·
CH3-Cl, Δ\Delta H° = 352 kJ mol-1
H-Cl, Δ\Delta H° = 432 kJ mol -1
This mechanism is unlikely because:

A) The overall Δ\Delta H° is highly endothermic.
B) The probability factor is low.
C) One of the chain propagating steps is non-productive.
D) One of the chain propagating steps has a very high Eact.
E) One of the chain propagating steps is highly exothermic.
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21
In the presence of light at 25°C,isobutane (1 mol)and bromine (1 mol)yield which monobromo product(s)?

A) 2-Methyl-1-bromopropane (almost exclusively)
B) 2-Methyl-2-bromopropane (almost exclusively)
C) A mixture of 50% (A)and 50% (B)
D) A mixture of 90% (A)and 10% (B)
E) Butyl bromide
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22
Which of the following reactions would have an activation energy equal to zero?

A) H-H \rightarrow 2H·
B) H· + CH3-H \rightarrow CH3--H + H·
C) CH3· + CH3· \rightarrow CH3-CH3
D) CH3· + CH3-H \rightarrow CH3-H + CH3·
E) All of the above
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23
Which of the following reactions would have the smallest energy of activation?

A)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following reactions would have the smallest energy of activation?</strong> A)   B)   C)   D)   E)
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24
Which of the following statements is true when used to compare the reaction of fluorine with 2-methylhexane and the reaction of bromine with 2-methylhexane?

A) Bromine is the less reactive and the less selective,giving 2-bromo-2-methyl hexane as one of several products.
B) Fluorine is the less reactive and the more selective,giving 2-fluoro-2-methyl hexane as the major product.
C) Fluorine is the more reactive and less selective,giving 2-fluoro-2-methyl hexane as one of several products.
D) Bromine is the more reactive and the more selective,giving 2-bromo-2-methyl hexane as the major product.
E) More than one of the above statements is true.
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25
For which of the following gas-phase reactions would the Eact be equal to Δ\Delta H°?

A) Cl-Cl \rightarrow 2Cl·
B) 2 Cl· \rightarrow Cl-Cl
C) Cl· + CH4 \rightarrow CH3· + H-Cl
D) CH3· + CH3· \rightarrow CH3-CH3
E) CH3· + Cl-Cl \rightarrow CH3-Cl + Cl·
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26
Which of the following reactions would have an activation energy equal to zero?

A) CH3-CH3 -- \rightarrow 2CH3·
B) H· + CH3CH3 -- \rightarrow CH3CH3 + H·
C) 2CH3CH2· -- \rightarrow CH3CH2CH2CH3
D) CH3· + CH3CH3 -- \rightarrow CH3CH3 + CH3·
E) None of the above
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27
Select the structure of the major product formed in the following reaction. <strong>Select the structure of the major product formed in the following reaction.  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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28
What feature would you expect to see in the 1H NMR spectrum of B after subjecting A to the following reaction? <strong>What feature would you expect to see in the <sup>1</sup>H NMR spectrum of B after subjecting A to the following reaction?  </strong> A) There would be only 4 aromatic protons at low field. B) The signal for the protons on the benzylic carbon would be a doublet. C) The signal for the methyl protons would be a triplet. D) The signal for the methyl protons would be a doublet. E) The signal for the methyl protons would integrate for only 2 hydrogens.

A) There would be only 4 aromatic protons at low field.
B) The signal for the protons on the benzylic carbon would be a doublet.
C) The signal for the methyl protons would be a triplet.
D) The signal for the methyl protons would be a doublet.
E) The signal for the methyl protons would integrate for only 2 hydrogens.
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29
At some temperatures,the relative reactivities of 3°,2° and 1° alkane hydrogens in free radical chlorination are in the ratio of 5:3:1.Thus,monochlorination of isopentane should produce these percentages of 2-chloro-2-methylbutane (A),combined 1-chloro-2-methylbutane and 1-chloro-3-methylbutane (B),and 2-chloro-3-methylbutane (C):

A) 8% A,75% B,17% C
B) 25% A,45% B,30% C
C) 29% A,44% B,18% C
D) 30% A,35% B,35% C
E) 36% A,43% B,21% C
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30
Which reaction would you expect to have the smallest energy of activation? Δ\Delta H°(kJ mol-1)

A) CH3· + CH3· -- \rightarrow CH3CH3 -378
B) CH4 + F· -- \rightarrow CH3· + HF -130
C) CH4 + I· -- \rightarrow CH3· + HI +142
D) CH4 + Br· -- \rightarrow CH3· + HBr +104
E) CH4 + Cl· -- \rightarrow CH3· + HCl +8
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31
An example of a reaction having an Eact = 0 would be:

A) Br· + Br-Br -- \rightarrow Br-Br + Br·
B) F· + CH4 -- \rightarrow H-F + CH3·
C) CH3· + Cl· -- \rightarrow CH3Cl
D) More than one of these
E) None of these
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32
What sequence of reactions could be used to prepare cis-1,2-cyclopentanediol from cyclopentane?

A) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)OsO4; (4)NaHSO3/H2O
B) (1)t-BuOK/t-BuOH; (2)Cl2,h ν\nu ; (3)NaOH/H2O
C) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)H2O2
D) (1)NaOH/H2O; (2)Br2; (3)NaNH2(2eq. )/liq.NH3; (4)KMnO4,NaOH/H2O,5°C
E) (1)Cl2,h ν\nu ; (2)t-BuOK/t-BuOH; (3)Hg(OAc)2,H2O (4)NaBH4,H3O+
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33
Which of the following reactions would have the smallest energy of activation?

A) CH4 + Br· \rightarrow CH3· + HBr
B) CH3CH3 + Br· \rightarrow CH3CH2· + HBr
C)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
D)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
E)
 <strong>Which of the following reactions would have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
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34
An example of a reaction having an Eact = 0 would be:

A) Br· + Br-Br \rightarrow Br-Br + Br·
B) F· + CH4 \rightarrow H-F + CH3·
C) CH3· + CH3CH3 \rightarrow CH4 + CH3CH2·
D) Br· + H-Br \rightarrow H-Br + Br·
E) CH3· + CH3· \rightarrow CH3-CH3
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35
Which reaction would you expect to have the largest energy of activation? Δ\Delta H° (kJ mol-1)

A) CH3· + CH3· \rightarrow CH3CH3 -378
B) CH3· + Br· \rightarrow CH3Br -130
C) CH4 + I· \rightarrow CH3· + HI +142
D) CH4 + Br· \rightarrow CH3· + HBr +104
E) CH4 + Cl· \rightarrow CH3· + HCl +8
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36
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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37
Which of the following reactions should have the smallest energy of activation?

A) CH4 + Cl· \rightarrow CH3· + HCl
B) CH3CH3 + Cl· \rightarrow CH3CH2· + HCl
C)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)
D)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)
E)
 <strong>Which of the following reactions should have the smallest energy of activation?</strong> A) CH<sub>4</sub> + Cl·  \rightarrow CH<sub>3</sub>· + HCl B) CH<sub>3</sub>CH<sub>3</sub> + Cl·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HCl C)   D)   E)
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38
When an alkane in which all hydrogen atoms are not equivalent is monosubstituted,use of this halogen produces a ratio of isomers which is essentially statistical,i.e. ,dependent only on the number of each type of hydrogen.

A) F2
B) Cl2
C) Br2
D) I2
E) All of the above
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39
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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40
Which is true for a chain-terminating step?

A) "A new free radical is formed."
B) "The process is endothermic."
C) "Eact = 0."
D) " Δ\Delta H° is positive."
E) "A product is formed which is immune to further reaction."
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41
For which reaction would the transition state be most product-like?

A) CH4 + Br· \rightarrow CH3· + HBr
B) CH3CH3 + Br· \rightarrow CH3CH2· + HBr
C)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
D)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
E)
 <strong>For which reaction would the transition state be most product-like?</strong> A) CH<sub>4</sub> + Br·  \rightarrow CH<sub>3</sub>· + HBr B) CH<sub>3</sub>CH<sub>3</sub> + Br·  \rightarrow  CH<sub>3</sub>CH<sub>2</sub>· + HBr C)   D)   E)
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42
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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43
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He

A) Ha
B) Hb
C) Hc
D) Hd
E) He
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44
Free radical mono-halogenation of an alkane is typically conducted using bromine versus chlorine because

A) the bromine radical is more reactive and therefore more selective.
B) the chlorine radical is more reactive and therefore more selective.
C) the chlorine radical is less reactive and therefore more selective.
D) the bromine radical is less reactive and therefore more selective.
E) None of the above
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45
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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46
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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47
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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48
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He

A) Ha
B) Hb
C) Hc
D) Hd
E) He
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49
What is the final product,C,obtained via the following reaction sequence? <strong>What is the final product,C,obtained via the following reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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50
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He

A) Ha
B) Hb
C) Hc
D) Hd
E) He
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51
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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52
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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53
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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54
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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55
What is the product for the following reaction sequence? <strong>What is the product for the following reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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56
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He

A) Ha
B) Hb
C) Hc
D) Hd
E) He
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57
Mono-bromination of the following alkane, <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V , (using Br2 with light)would be? <strong>Mono-bromination of the following alkane,   , (using Br<sub>2</sub> with light)would be?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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58
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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59
Which hydrogen would be abstracted first when mono-brominating with Br2 and light? <strong>Which hydrogen would be abstracted first when mono-brominating with Br<sub>2</sub> and light?  </strong> A) Ha B) Hb C) Hc D) Hd E) He

A) Ha
B) Hb
C) Hc
D) Hd
E) He
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60
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> 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
The free radical chlorination of pentane produces this number of monochloro compounds,including stereoisomers.

A) 2
B) 3
C) 4
D) 5
E) 6
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62
The free radical chlorination of 3-chloropentane forms a mixture of dichloropentanes which,on precise fractional distillation,affords these fractions:

A) 4 fractions,none optically active
B) 4 fractions,2 optically active
C) 7 fractions,4 optically active
D) 7 fractions,6 optically active
E) 7 fractions,all optically active
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63
More than one monochloro compound can be obtained from the free radical chlorination of:

A) Cyclopentane
B) Neopentane
C) Isobutane
D) Ethane
E) Methane
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64
The p-orbital of a methyl radical carbon,CH3·,contains how many electrons?

A) 1
B) 2
C) 3
D) 4
E) 0
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65
What product would result from the following reaction? <strong>What product would result from the following reaction?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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66
What is the total number of trichloropropanes which can be produced by free radical chlorination of propane? Include all stereoisomers.

A) 4
B) 5
C) 6
D) 7
E) 8
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67
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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68
Free radical chlorination of hexane produces this number of monochloro derivatives (including stereoisomers):

A) 3
B) 4
C) 5
D) 7
E) 8
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69
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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70
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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71
How many monochloro derivatives,including stereoisomers,can be formed in the chlorination of 1-bromobutane?

A) 4
B) 5
C) 6
D) 7
E) 8
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72
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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73
The reaction of 1-butene with HBr in the presence of peroxides yields 1-bromobutane.The mechanism for the reaction involves:

A) attack on the alkene by a Br+ ion.
B) attack on the alkene by a H+ ion.
C) attack on the alkene by a bromine atom,Br·.
D) attack on the alkene by a hydrogen atom,H·.
E) isomerization of the 2-bromobutane produced initially.
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74
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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75
What is the product for the following three-step reaction sequence? <strong>What is the product for the following three-step reaction sequence?  </strong> A) I B) II C) III D) IV E) V

A) I
B) II
C) III
D) IV
E) V
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76
Which of the following would serve as the best synthesis of 2-bromohexane?

A)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable.
B)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable.
C)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable.
D)
<strong>Which of the following would serve as the best synthesis of 2-bromohexane?</strong> A)   B)   C)   D)   E) All of the above would be equally suitable.
E) All of the above would be equally suitable.
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77
The free radical chlorination of (R)-2-chloropentane forms a mixture of dichloropentanes which includes:

A) three optically active compounds.
B) two achiral compounds.
C) two meso compounds.
D) one pair of diastereomers.
E) one racemic mixture.
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78
Consider the light-initiated chlorination of (S)-2-chlorobutane followed by careful fractional distillation (or separation by GLC)of all of the products with the formula C4H8Cl2.How many fractions (in total)would be obtained and how many of these fractions would be optically active?

A) Three fractions total;all optically active
B) Four fractions total;three fractions optically active
C) Five fractions total;all optically active
D) Five fractions total;four fractions optically active
E) Five fractions total;three fractions optically active
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79
Free radical chlorination will produce but one monochloro derivative in the case of:

A) Propane
B) Butane
C) Isobutane
D) Isopentane
E) Neopentane
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80
Which of the following combinations of reactants can provide a demonstrable example of anti-Markovnikov addition?

A) CH2=CHCH3 + HCl + ROOR
B) CH3CH=CH2 + H2O + Cl2
C) CH3CH=CHCH3 + HBr + ROOR
D) CH3CH2CH=CH2 + HBr + ROOR
E) CH3CH2CH=CH2 + Br2 + ROOR
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Unlock Deck
Unlock for access to all 114 flashcards in this deck.