A) a meso dibromide.
B) a mixture of optically active enantiomeric dibromides.
C) a mixture of optically inactive enantiomeric dibromides.
D) (Z) -3,4-dibromo-3-hexene.
E) (E) -3,4-dibromo-3-hexene.
Correct Answer
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Multiple Choice
A) the product is statistically favored.
B) steric hindrance favors its formation.
C) the reaction proceeds via the more/most stable carbocation.
D) the reaction forms the more/most stable product.
E) All of the above are valid reasons
Correct Answer
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Short Answer
Correct Answer
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Multiple Choice
A) 2-iodopentane
B) 2-iodo-2-methylbutane
C) 1-iodo-2-methylbutane
D) 2-iodo-1-methylbutane
E) 3-iodo-2-methylbutane
Correct Answer
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Multiple Choice
A) Addition and elimination reactions are favored at low temperatures.
B) Addition and elimination reactions are favored at high temperatures.
C) Only addition reactions are favored at low temperatures.
D) Only elimination reactions are favored at low temperatures.
E) Addition and elimination reactions are disfavored at low temperatures.
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Multiple Choice
A) The positive entropy term dominates at high temperature.
B) The negative entropy term dominates at high temperature.
C) The positive enthalpy term dominates at high temperature.
D) The negative enthalpy term dominates at high temperature.
E) The enthalpy and entropy terms cancel at high temperature.
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Multiple Choice
A) 1-Chloro-2-methylbutane
B) 1-Chloro-3-methylbutane
C) 2-Chloro-2-methylbutane
D) 2-Chloro-3-methylbutane
E) 1-Chloropentane
Correct Answer
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Multiple Choice
A) dihydroxylation using OsO4,H2O2
B) addition of H2
C) hydroboration
D) addition of HCl
E) A,B,and C
Correct Answer
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Multiple Choice
A) Markovnikov orientation with syn-addition
B) Markovnikov orientation with anti-addition
C) anti-Markovnikov orientation with syn-addition
D) anti-Markovnikov orientation with anti-addition
E) Markonikov orientation with both syn- and anti-addition
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Multiple Choice
A) formation of a π bond
B) addition of two groups across a double bond
C) breaking of a π bond
D) A and B
E) B and C
Correct Answer
verified
Multiple Choice
A) 1
B) 2
C) 3
D) 4
E) 5
Correct Answer
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Multiple Choice
A) 2-methyl-1-pentene2
B) 2-methyl-2-pentene
C) 4-methyl-2-pentene
D) 4-methyl-1-pentene
E) All of the above
Correct Answer
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Short Answer
Correct Answer
verified
Multiple Choice
A) 12
B) 2
C) 3
D) 4
E) None of the above
Correct Answer
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Multiple Choice
A) Markovnikov orientation with syn-addition
B) Markovnikov orientation with anti-addition
C) anti-Markovnikov orientation with syn-addition
D) anti-Markovnikov orientation with anti-addition
E) Markonikov orientation with both syn- and anti-addition
Correct Answer
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Multiple Choice
A) No reaction
B) cis-1,2-dimethylcyclohexane
C) trans-3,4-dimethylhexane
D) trans-1,2-dimethylhexane
E) None of the above
Correct Answer
verified
Multiple Choice
A) ether
B) epoxide
C) alkane
D) syn diol
E) alkyne
Correct Answer
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Multiple Choice
A) the positive enthalpy term is larger than the negative entropy term.
B) the negative enthalpy term is larger than the positive entropy term.
C) the positive enthalpy term is smaller than the negative entropy term.
D) the negative enthalpy term is smaller than the positive entropy term.
E) the enthalpy and entropy terms are equal.
Correct Answer
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Multiple Choice
A) I
B) II
C) III
D) I and II
E) II and III
Correct Answer
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Multiple Choice
A) the breaking of a π and bond.
B) the formation of two bonds.
C) the reaction being exothermic.
D) two molecules reacting to form a single molecule.
E) the temperature dependence of the S term.
Correct Answer
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