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Provide the structure of reactant (X) for the following reaction. Provide the structure of reactant (X) for the following reaction. A) I B) II C) III D) IV E) V Provide the structure of reactant (X) for the following reaction. A) I B) II C) III D) IV E) V Provide the structure of reactant (X) for the following reaction. A) I B) II C) III D) IV E) V


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

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Which one of the following compounds is most acidic?


A) ethyl acetoacetate
B) 2-butanone
C) ethyl pentanoate
D) 1-butanol
E) 3-pentanone

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Predict the product for the following reaction. Predict the product for the following reaction. A) I B) II C) III D) IV E) V Predict the product for the following reaction. A) I B) II C) III D) IV E) V Predict the product for the following reaction. 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 reagents necessary to carry out the following conversion. Provide the reagents necessary to carry out the following conversion.

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1. NaOH/I2
...

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Provide the reactants that will yield the following compound as a crossed Claisen condensation product. Provide the reactants that will yield the following compound as a crossed Claisen condensation product.

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Which one of the following compounds can be prepared using the Michael reaction? Which one of the following compounds can be prepared using the Michael reaction? A) I B) II C) III D) IV E) none of these


A) I
B) II
C) III
D) IV
E) none of these

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Which one of the following reaction sequences will yield 2,2-dimethylcyclohexane-1,3-dione. Which one of the following reaction sequences will yield 2,2-dimethylcyclohexane-1,3-dione. A) I B) II C) III D) IV E) II and IV Which one of the following reaction sequences will yield 2,2-dimethylcyclohexane-1,3-dione. A) I B) II C) III D) IV E) II and IV Which one of the following reaction sequences will yield 2,2-dimethylcyclohexane-1,3-dione. A) I B) II C) III D) IV E) II and IV Which one of the following reaction sequences will yield 2,2-dimethylcyclohexane-1,3-dione. A) I B) II C) III D) IV E) II and IV


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

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


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

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Predict the major product(s) for the following reaction. Predict the major product(s) for the following reaction. A) I B) II and IV C) III D) I and III E) V Predict the major product(s) for the following reaction. A) I B) II and IV C) III D) I and III E) V Predict the major product(s) for the following reaction. A) I B) II and IV C) III D) I and III E) V


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

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Provide the reagents necessary to carry out the following conversion using a malonic ester synthesis. Provide the reagents necessary to carry out the following conversion using a malonic ester synthesis.

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1. NaOCH2CH3
2. (CH3)2CH...

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


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

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Which of the following compounds can be prepared using the Dieckmann condensation? Which of the following compounds can be prepared using the Dieckmann condensation? A) I B) II C) III D) IV E) II and IV


A) I
B) II
C) III
D) IV
E) II and 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. H3O+/heat...

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Which of the following compounds would NOT undergo racemization in the presence of a base? Which of the following compounds would NOT undergo racemization in the presence of a base? A) I B) II C) III D) IV E) II and III


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

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Provide the reactants that would give the following aldol condensation product. Provide the reactants that would give the following aldol condensation product.

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Provide the reactants that would give the following aldol condensation product. Provide the reactants that would give the following aldol condensation product. A) I B) II C) III D) IV E) none of these Provide the reactants that would give the following aldol condensation product. A) I B) II C) III D) IV E) none of these Provide the reactants that would give the following aldol condensation product. A) I B) II C) III D) IV E) none of these Provide the reactants that would give the following aldol condensation product. A) I B) II C) III D) IV E) none of these Provide the reactants that would give the following aldol condensation product. A) I B) II C) III D) IV E) none of these


A) I
B) II
C) III
D) IV
E) none of these

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Provide the reactant(s) that would give the following possible aldol condensation product. Provide the reactant(s) that would give the following possible aldol condensation product.

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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) all of these Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) all of these Predict the product(s) for the following reaction. A) I B) II C) III D) IV E) all of these


A) I
B) II
C) III
D) IV
E) all of these

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

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Which of the following bases will completely convert 1,4-cyclohexanedione into an enolate?


A) sodium hydroxide
B) sodium ethoxide
C) LDA
D) sodium hydride
E) both C and D

Correct Answer

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Showing 101 - 120 of 147

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