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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?

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Identify the products of a reaction under kinetic control.


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

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Identify the cumulated diene.


A) 4-methyl-1,3-heptadiene
B) 3-methyl-1,5-heptadiene
C) 2-methyl-2,4-heptadiene
D) 4-methyl-1,4-heptadiene
E) 5-methyl-2,3-heptadiene

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

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Provide the structure of the 1,2 addition product for the following reaction. Provide the structure of the 1,2 addition product for the following reaction.

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Which of the following is true of pericyclic reactions?


A) they are concerted reactions
B) proceed via a cyclic transition state
C) no intermediates are formed
D) all of these

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

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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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Identify the pericyclic reaction in which no sigma bonds are formed and no pi bonds are broken.


A) sigmatropic rearrangement
B) cycloaddition reaction
C) electrolytic reaction
D) this is not a pericyclic reaction

E) A) and D)
F) B) and C)

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Predict the major product for the following intramolecular Diels-Alder reaction and provide a curved arrow mechanism for the formation of the product. Predict the major product for the following intramolecular Diels-Alder reaction and provide a curved arrow mechanism for the formation of the product.

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

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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-5,6-diethyl-1,3-cyclohexadiene B)  conrotatory, cis-5,6-diethyl-1,3-cyclohexadiene C)  disrotatory, trans-5,6-diethyl-1,3-cyclohexadiene D)  conrotatory, trans -5,6-diethyl-1,3-cyclohexadiene


A) disrotatory, cis-5,6-diethyl-1,3-cyclohexadiene
B) conrotatory, cis-5,6-diethyl-1,3-cyclohexadiene
C) disrotatory, trans-5,6-diethyl-1,3-cyclohexadiene
D) conrotatory, trans -5,6-diethyl-1,3-cyclohexadiene

E) A) and C)
F) B) and D)

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Identify the color of a compound that absorbs blue light.


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

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

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

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Use Woodward-Fieser rules to estimate the λ\lambda max for the following compound.  Use Woodward-Fieser rules to estimate the  \lambda <sub>max</sub> for the following compound.

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Which of the following compounds has the longest λ\lambda max?


A) (E ) -2-pentene
B) (Z) -2-pentene
C) 1-pentene
D) 1,3-hexadiene
E) 1,3,5-hexatriene

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

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Use Woodward-Fieser rules to estimate the λ\lambda max for the following compound.  Use Woodward-Fieser rules to estimate the  \lambda <sub>max</sub> for the following compound.

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Predict the product(s) for the following reaction. Predict the product(s)  for the following reaction.     A)  I B)  II C)  III D)  IV E)  both I & III Predict the product(s)  for the following reaction.     A)  I B)  II C)  III D)  IV E)  both I & III


A) I
B) II
C) III
D) IV
E) both I & III

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

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Rank the following dienes in order of decreasing heat of hydrogenation (highest to lowest). Rank the following dienes in order of decreasing heat of hydrogenation (highest to lowest).

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Zingiberene, a terpene found in ginger, has the following structure. Classify the π\pi bonds in zingiberene as conjugated, cumulated or isolated.  Zingiberene, a terpene found in ginger, has the following structure. Classify the  \pi bonds in zingiberene as conjugated, cumulated or isolated.

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The reaction of 1,3-butadiene with hydrogen halide at 40°C will undergo _____ -addition under ____________ control.

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

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