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The Heck reaction requires the presence of a base.

A) True
B) False

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Which catalysts are common in the Stille coupling reaction?


A) Pd(PPh3) 4
B) Pd (OAc) 2
C) PdCl2(PPh3) 2
D) All of the above

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

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What is the product of the following sequence? What is the product of the following sequence?        A) I B) II C) III D) IV E) none of the them What is the product of the following sequence?        A) I B) II C) III D) IV E) none of the them What is the product of the following sequence?        A) I B) II C) III D) IV E) none of the them


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

F) C) and E)
G) None of the above

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What is the product of the following ring-closing metathesis reaction? What is the product of the following ring-closing metathesis reaction?     A)  I B)  II C)  III D)  IV What is the product of the following ring-closing metathesis reaction?     A)  I B)  II C)  III D)  IV


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

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

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Which of the following compounds has the most nucleophilic carbon atom? Which of the following compounds has the most nucleophilic carbon atom?   A)  I B)  II C)  III D)  IV


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

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

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What product(s) result in the following reaction? Select all that apply. What product(s)  result in the following reaction? Select all that apply.        A) I B) II C) III D) IV What product(s)  result in the following reaction? Select all that apply.        A) I B) II C) III D) IV What product(s)  result in the following reaction? Select all that apply.        A) I B) II C) III D) IV


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

E) B) and C)
F) None of the above

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Which of the following are advantages of the Suzuki coupling over the Stille coupling? Select all that apply.


A) Organoboron compounds are less expensive than organotin compounds.
B) Organoboron compounds are less toxic than organotin compounds.
C) Formation of alkyl-aryl bonds is possible.
D) The reaction requires a base.

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

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Draw the product(s) of the following reaction: Draw the product(s) of the following reaction:

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Identify the coupling partners that can be used to prepare the following compound in a Heck reaction. Identify the coupling partners that can be used to prepare the following compound in a Heck reaction.   A)  p-nitrostyrene and (E) -(2-bromovinyl) benzene B)  p-nitrostyrene and (Z) -(2-bromovinyl) benzene C)  (E) -1-(2-bromovinyl) -4-nitrobenzene and styrene D)  (Z) -1-(2-bromovinyl) -4-nitrobenzene and styrene


A) p-nitrostyrene and (E) -(2-bromovinyl) benzene
B) p-nitrostyrene and (Z) -(2-bromovinyl) benzene
C) (E) -1-(2-bromovinyl) -4-nitrobenzene and styrene
D) (Z) -1-(2-bromovinyl) -4-nitrobenzene and styrene

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

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What is the product of the following reaction? What is the product of the following reaction?

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Explain why the solvent for a Grignard reaction must be free of water.

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Water cons...

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What is the product of the following reaction? What is the product of the following reaction?   A)  (E) -1-phenyl-1-pentene B)  (Z) -1-phenyl-1-pentene C)  (E) -1-phenyl-2-pentene D)  (Z) -1-phenyl-2-pentene E)  2-phenyl-1-pentene


A) (E) -1-phenyl-1-pentene
B) (Z) -1-phenyl-1-pentene
C) (E) -1-phenyl-2-pentene
D) (Z) -1-phenyl-2-pentene
E) 2-phenyl-1-pentene

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

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Which of the following Gilman reagents could be used with a vinyl halide to afford the (E,E) -diene shown below? Select all that apply. Which of the following Gilman reagents could be used with a vinyl halide to afford the (E,E) -diene shown below? Select all that apply.         A)  I B)  II C)  III D)  IV E)  II and III Which of the following Gilman reagents could be used with a vinyl halide to afford the (E,E) -diene shown below? Select all that apply.         A)  I B)  II C)  III D)  IV E)  II and III Which of the following Gilman reagents could be used with a vinyl halide to afford the (E,E) -diene shown below? Select all that apply.         A)  I B)  II C)  III D)  IV E)  II and III Which of the following Gilman reagents could be used with a vinyl halide to afford the (E,E) -diene shown below? Select all that apply.         A)  I B)  II C)  III D)  IV E)  II and III


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

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

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Which of the following R groups (R-SnBu3) would undergo the slowest transmetallation in a Stille coupling reaction?


A) alkyl
B) aryl
C) vinyl
D) benzyl

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

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Which of the following R groups (R-SnBu3) would undergo the fastest transmetallation in a Stille coupling reaction?


A) alkyl
B) aryl
C) vinyl
D) benzyl

E) None of the above
F) C) and D)

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Which of the following would react fastest in the Corey-Posner/Whitesides-House reaction?


A) cyclohexyl chloride
B) cyclohexyl iodide
C) tert-butyl chloride
D) tert-butyl iodide

E) None of the above
F) All of the above

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Identify the product when butanal reacts with one equivalent of a Grignard reagent.


A) primary alcohol
B) secondary alcohol
C) tertiary alcohol
D) carboxylic acid
E) ketone

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

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Which of the following statements is false regarding the reactivity of Gilman reagents?


A) They react with acyl halides to give ketones.
B) They react with α,β-unsaturated ketones to give alcohols.
C) They react with alkyl halides or aryl halides in a coupling reaction.
D) They are unreactive with tertiary halides.

E) None of the above
F) B) and D)

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What is the product of the following sequence? What is the product of the following sequence?

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Which of the following compounds has the most ionic character in the C-M bond?


A) HC≡CMgBr
B) HC≡CK
C) HC≡CNa
D) HC≡CLi

E) B) and C)
F) None of the above

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