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Which major product(s) is(are) formed in the following reaction? Which major product(s)  is(are)  formed in the following reaction?     A)  I and V B)  II and IV C)  III and IV D)  I, III and VI E)  II, IV and V Which major product(s)  is(are)  formed in the following reaction?     A)  I and V B)  II and IV C)  III and IV D)  I, III and VI E)  II, IV and V


A) I and V
B) II and IV
C) III and IV
D) I, III and VI
E) II, IV and V

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The following Diels-Alder reaction product is an intermediate in the synthesis of estrone. Provide the structure of the product. The following Diels-Alder reaction product is an intermediate in the synthesis of estrone. Provide the structure of the product.

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Which of the following diene(s) cannot undergo the Diels-Alder reaction? Which of the following diene(s)  cannot undergo the Diels-Alder reaction?   A)  I B)  II C)  III D)  IV E)  I & IV


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

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Dienes with adjacent π bonds are classified as ______.


A) isolated
B) cumulated
C) skipped
D) conjugated
E) none of these

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Provide the structure for (Z)-2-methyl-2,4-hexadiene.

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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

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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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1. H2SO4, he...

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How many electrons does the HOMO of 1,3-pentadiene have in its excited state?


A) 1
B) 2
C) 3
D) 4
E) none

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Identify the product of a thermodynamically-controlled reaction.


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

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Identify the MOs that react to form cyclohexene.


A) HOMO of 1,3-butadiene and LUMO of ethylene
B) LUMO of 1,3-butadiene and LUMO of ethylene
C) HOMO of 1,3-butadiene and HOMO of ethylene
D) LUMO of 1,3-butadiene and LUMO of 1,3-butadiene
E) HOMO of 1,3-butadiene and HOMO of 1,3-butadiene

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Predict the product for the following Claisen rearrangement. Predict the product for the following Claisen rearrangement.       A)  I B)  II C)  III D)  IV E)  V Predict the product for the following Claisen rearrangement.       A)  I B)  II C)  III D)  IV E)  V Predict the product for the following Claisen rearrangement.       A)  I B)  II C)  III D)  IV E)  V


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

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Provide the structures of A, B and C for the following reaction sequence. Provide the structures of A, B and C for the following reaction sequence.

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Rank the following dienes in order of increasing stability (least to most) . Rank the following dienes in order of increasing stability (least to most) .   A)  I < IV < III < II B)  III < II < I < IV C)  IV < II < III < I D)  II < IV < III < I E)  IV < III < II < I


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

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Predict the product for the following reaction and provide the curved arrow mechanism for the formation of the product. Predict the product for the following reaction and provide the curved arrow mechanism for the formation of the product.

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blured image_TB4454_00...

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The following product is formed by an intramolecular Diels-Alder reaction. Provide the structure of the starting compound. The following product is formed by an intramolecular Diels-Alder reaction. Provide the structure of the starting compound.

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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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IV > V > I...

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Which is the most energetically favorable UV transition for 1,3-butadiene?


A) (n \to σ\sigma *)
B) (n \to π\pi *)
C) ( π\pi 2 \to π\pi 3*)
D) ( σ\sigma \to σ\sigma *)
E) ( π\pi 1 \to π\pi 4*)

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What is the IUPAC name for the following compound? What is the IUPAC name for the following compound?   A)  1-chloro-1-methyl-2,5-cyclohexadiene B)  3-chloro-3-methyl-1,4-cyclohexadiene C)  6-chloro-6-methyl-1,4-cyclohexadiene D)  2-chloro-2-methyl-1,3-cyclohexadiene E)  None of these


A) 1-chloro-1-methyl-2,5-cyclohexadiene
B) 3-chloro-3-methyl-1,4-cyclohexadiene
C) 6-chloro-6-methyl-1,4-cyclohexadiene
D) 2-chloro-2-methyl-1,3-cyclohexadiene
E) None of these

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Identify the conjugated diene(s) . Identify the conjugated diene(s) .   A)  I B)  II C)  III D)  IV E)  II & IV


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

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Which one of the following dienes will have the lowest heat of hydrogenation? Which one of the following dienes will have the lowest heat of hydrogenation?   A)  I B)  II C)  III D)  IV E)  V


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

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