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Provide the major organic product(s) of the reaction shown below. Provide the major organic product(s) of the reaction shown below.

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Draw a correct structure for the reaction below. Draw a correct structure for the reaction below.

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Starting from benzene, how would you make the following compound? Starting from benzene, how would you make the following compound?

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1) Br2, FeB...

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Which of the following compounds will not undergo Friedel-Crafts acylation when treated with Which of the following compounds will not undergo Friedel-Crafts acylation when treated with   A)  toluene B)  p-xylene C)  anisole D)  ethoxybenzene E)  benzophenone


A) toluene
B) p-xylene
C) anisole
D) ethoxybenzene
E) benzophenone

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Complete the following reaction by filling in the necessary reagents. Complete the following reaction by filling in the necessary reagents.

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Provide the major organic product of the following reaction. Provide the major organic product of the following reaction.

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Predict the products from the following reaction. Predict the products from the following reaction.

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Provide the structure of the major organic product in the following reaction. Provide the structure of the major organic product in the following reaction.

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Provide the major organic product of the following reaction. Provide the major organic product of the following reaction.

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Which of the following is an intermediate in the bromination of toluene?


A) Which of the following is an intermediate in the bromination of toluene? A)    B)    C)    D)
B) Which of the following is an intermediate in the bromination of toluene? A)    B)    C)    D)
C) Which of the following is an intermediate in the bromination of toluene? A)    B)    C)    D)
D) Which of the following is an intermediate in the bromination of toluene? A)    B)    C)    D)

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Provide the structure of the major organic product in the following reaction. Provide the structure of the major organic product in the following reaction.

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p-Methoxybenzaldehyde can be prepared from anisole using the Gatterman-Koch formylation. What mixture of reagents is necessary for this process?


A) CO, HCl, AlCl3, CuCl
B) CO, SO3, H2SO4
C) CO2, HCl, AlCl3
D) CO2, SO3, H2SO4
E) CO2, HNO3, H2SO4

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Which of the following compounds will undergo bromination least rapidly when treated with Br2 and FeBr3?


A) p-methylacetanilide
B) bromobenzene
C) acetanilide
D) benzenesulfonic acid
E) benzene

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Which series of reagents would be required to perform the following synthesis? Which series of reagents would be required to perform the following synthesis?   A)  1. ClCH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>, AlCl<sub>3</sub> 2. FeBr<sub>3</sub>, Br<sub>2</sub> B)  1. ClCOCH<sub>2</sub>CH<sub>3</sub>, AlCl<sub>3</sub> 2. FeBr<sub>3</sub>, Br<sub>2</sub> C)  1. ClCOCH<sub>2</sub>CH<sub>3</sub>, AlCl<sub>3</sub> 2. FeBr<sub>3</sub>, Br<sub>2</sub> 3. Zn(Hg) , HCl D)  1. ClCOCH<sub>2</sub>CH<sub>3</sub>, AlCl<sub>3 </sub>2. Zn(Hg) , HCl 3. FeBr<sub>3</sub>, Br<sub>2</sub>


A) 1. ClCH2CH2CH3, AlCl3 2. FeBr3, Br2
B) 1. ClCOCH2CH3, AlCl3 2. FeBr3, Br2
C) 1. ClCOCH2CH3, AlCl3 2. FeBr3, Br2 3. Zn(Hg) , HCl
D) 1. ClCOCH2CH3, AlCl3 2. Zn(Hg) , HCl 3. FeBr3, Br2

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Show how the following product can be made from benzene. Show how the following product can be made from benzene.

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1) isobutyryl chlori...

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Provide the major organic product of the following reaction. Provide the major organic product of the following reaction.

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Explain why -OCH3 is a stronger activator than -OCOCH3.

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Both substituents have nonbonding electr...

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Which sequence correctly ranks the following aromatic rings in order of increasing rate of reactivity in an electrophilic aromatic substitution reaction? Which sequence correctly ranks the following aromatic rings in order of increasing rate of reactivity in an electrophilic aromatic substitution reaction?   A)  1 < 2 < 3 B)  2 < 3 < 1 C)  3 < 1 < 2 D)  2 < 1 < 3


A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 2 < 1 < 3

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Provide the major organic product of the following reaction. Provide the major organic product of the following reaction.

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Draw a mechanism for the reaction shown below. Draw a mechanism for the reaction shown below.

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