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A thermodynamically-controlled reaction will yield :


A) the most stable product.
B) the product whose formation requires the smallest free energy of activation.
C) the product that can be formed in the fewest steps.
D) the product that is formed at the fastest rate.
E) None of these.

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

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What is the correct classification of the following pericyclic reaction? What is the correct classification of the following pericyclic reaction?   A)  electrophilic addition B)  sigmatropic rearrangement C)  cycloaddition D)  electrocyclic reaction E)  C & D


A) electrophilic addition
B) sigmatropic rearrangement
C) cycloaddition
D) electrocyclic reaction
E) C & D

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

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Which of the following compounds is an isolated diene? Which of the following compounds is an isolated diene?   A)  I B)  II C)  III D)  IV E)  V


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

F) B) and D)
G) A) and B)

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Predict the major product for the following Diels-Alder reaction. Predict the major product for the following Diels-Alder reaction.

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Which one of the following dienes is most stable?


A) CH3CH=CHCH=CHCH3
B) CH3CH=CHCH2CH=CH2
C) CH2=CHCH2CH2CH=CH2
D) CH2=CHCH(CH3) CH=CH2
E) CH3CH=C=CHCH2CH3

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

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Provide the reagents necessary to carry out the following conversion. Provide the reagents necessary to carry out the following conversion.

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Predict the major product for the following Diels-Alder reaction. Predict the major product for the following Diels-Alder reaction.

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Which of the following compounds have conjugated double bonds? Which of the following compounds have conjugated double bonds?

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Predict the possible major products for the following reaction. Predict the possible major products for the following reaction.

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Identify the color of a compound that absorbs yellow light.


A) orange
B) green
C) red
D) blue
E) violet

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

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Predict the product for the following reaction. Predict the product for the following reaction.

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Predict the major product for the following reaction and explain why it is major product. Predict the major product for the following reaction and explain why it is major product.

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blured image This reaction is under thermodynamic co...

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Which diene and dienophile would react to give the following Diels-Alder product? Which diene and dienophile would react to give the following Diels-Alder product?     A)  I B)  II C)  III D)  IV E)  V Which diene and dienophile would react to give the following Diels-Alder product?     A)  I B)  II C)  III D)  IV E)  V


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

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

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Provide the structure for (S,E)-3-t-butyl-4-methyl-1,4-hexadiene.

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Which one of the following dienophiles is most reactive in the Diels-Alder reaction? Which one of the following dienophiles is most reactive in the Diels-Alder reaction?   A)  I B)  II C)  III D)  IV E)  V


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

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

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Which of the following best describes the stereochemistry of ring closure and the product for the following reaction? Which of the following best describes the stereochemistry of ring closure and the product for the following reaction?   A)  disrotatory, cis-3,4-diethylcyclobutene B)  conrotatory, cis-3,4-diethylcyclobutene C)  disrotatory, trans-3,4-diethylcyclobutene D)  conrotatory, trans-3,4-diethylcyclobutene


A) disrotatory, cis-3,4-diethylcyclobutene
B) conrotatory, cis-3,4-diethylcyclobutene
C) disrotatory, trans-3,4-diethylcyclobutene
D) conrotatory, trans-3,4-diethylcyclobutene

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

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Predict the major product for the following Diels-Alder reaction. Predict the major product for the following Diels-Alder reaction.

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Which one of the following represents the highest energy π\pi -antibonding molecular orbital of 1,3-butadiene?  Which one of the following represents the highest energy   \pi -antibonding molecular orbital of 1,3-butadiene?   A)  I B)  II C)  III D)  IV


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

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

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Compound A is one of the intermediate products in the synthesis of the corticoid hormone cortisone. Provide the structure of compound A. Compound A is one of the intermediate products in the synthesis of the corticoid hormone cortisone. Provide the structure of compound A.

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What is the correct classification of the following pericyclic reaction? What is the correct classification of the following pericyclic reaction?   A)  electrophilic addition B)  sigmatropic rearrangement C)  cycloaddition D)  electrocyclic reaction E)  C & D


A) electrophilic addition
B) sigmatropic rearrangement
C) cycloaddition
D) electrocyclic reaction
E) C & D

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

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