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Provide the structure of the major organic product in the reaction below. Provide the structure of the major organic product in the reaction below.

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Which reaction intermediate is formed when Br2/CCl4 reacts with cyclohexene? Which reaction intermediate is formed when Br<sub>2</sub>/CCl<sub>4</sub> reacts with cyclohexene? A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

F) A) and E)
G) A) and D)

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What is hyperconjugation,and how does it affect carbocation stability?

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Delocalization of electrons by the overl...

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Predict the product of the following reaction. Predict the product of the following reaction.

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Provide the major organic product(s)in the reaction below. Provide the major organic product(s)in the reaction below.

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Draw the major organic product generated in the reaction below. Draw the major organic product generated in the reaction below.

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Draw the major organic product generated in the reaction below. Draw the major organic product generated in the reaction below.

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Provide the major organic product in the reaction below. Provide the major organic product in the reaction below. A) B) C) D) E)


A) Provide the major organic product in the reaction below. A) B) C) D) E)
B) Provide the major organic product in the reaction below. A) B) C) D) E)
C) Provide the major organic product in the reaction below. A) B) C) D) E)
D) Provide the major organic product in the reaction below. A) B) C) D) E)
E) Provide the major organic product in the reaction below. A) B) C) D) E)

F) B) and E)
G) A) and E)

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Provide the structure of the major organic product in the reaction below. Provide the structure of the major organic product in the reaction below.

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A reaction in which a mixture of two constitutional isomers is obtained but one is formed in higher amounts than the other is called a


A) regioselective reaction.
B) regiospecific reaction.
C) stereospecific reaction.
D) stereoselective reaction.
E) successful reaction.

F) C) and D)
G) A) and D)

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Draw the major organic product generated in the reaction below. Draw the major organic product generated in the reaction below.

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What configurations are found in the product(s) of the reaction below? What configurations are found in the product(s) of the reaction below? A) 1R,2R only B) 1S,2S only C) 1R,2S only D) an equal mixture of 1R,2R and 1S,2S E) an equal mixture of 1R,2R and 1R,2S


A) 1R,2R only
B) 1S,2S only
C) 1R,2S only
D) an equal mixture of 1R,2R and 1S,2S
E) an equal mixture of 1R,2R and 1R,2S

F) C) and E)
G) A) and D)

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The product of this reaction is called a(n) The product of this reaction is called a(n) A) peroxide. B) peroxy. C) epoxy. D) epoxide. E) oxide.


A) peroxide.
B) peroxy.
C) epoxy.
D) epoxide.
E) oxide.

F) None of the above
G) A) and B)

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Predict the product of the following reaction. Predict the product of the following reaction.

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Provide the major organic product(s)in the reaction below. Provide the major organic product(s)in the reaction below.

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In the following ozonolysis reaction,if we start with optically pure S-enantiomer,the product obtained will be In the following ozonolysis reaction,if we start with optically pure S-enantiomer,the product obtained will be A) racemic mixture. B) unequal mixture of R and S enantiomers. C) diastereomers. D) meso compounds. E) optically pure S-enantiomer.


A) racemic mixture.
B) unequal mixture of R and S enantiomers.
C) diastereomers.
D) meso compounds.
E) optically pure S-enantiomer.

F) All of the above
G) C) and D)

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For an endergonic reaction step,the Hammond postulate allows one to say that


A) the transition state of the step resembles the reactants of the step.
B) the transition state of the step resembles the products of the step.
C) the step is rate-determining since it has the smallest Ea.
D) the reaction containing this step is overall first order.
E) the transition state is precisely symmetric with bond-breaking and bond-forming occurring to the same extent.

F) All of the above
G) B) and E)

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Draw the products. Draw the products.

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Identify the most stable carbocation.


A) Identify the most stable carbocation. A) B) C) D) E)
B) Identify the most stable carbocation. A) B) C) D) E)
C) Identify the most stable carbocation. A) B) C) D) E)
D) Identify the most stable carbocation. A) B) C) D) E)
E) Identify the most stable carbocation. A) B) C) D) E)

F) D) and E)
G) C) and E)

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Propose a mechanism for the following reaction: Propose a mechanism for the following reaction:

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