Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions

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Instructions: Predict the products from the information given for the following question(s). -Predict:Instructions: Predict the products from the information given for the following question(s).  -Predict:

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Instructions: Predict the products from the information given for the following question(s). -Predict:Instructions: Predict the products from the information given for the following question(s). -Predict:

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Which of the following would correctly describe the respective 13C NMR and 1H NMR spectra for the indicated atoms for the compound shown below? Which of the following would correctly describe the respective <sup>13</sup>C NMR and <sup>1</sup>H NMR spectra for the indicated atoms for the compound shown below?

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C

Instructions: Consider the data below to answer the following question(s). C7H14O Instructions: Consider the data below to answer the following question(s). C<sub>7</sub>H<sub>14</sub>O      -Refer to instructions.What functional group is indicated by the IR data? -Refer to instructions.What functional group is indicated by the IR data?

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?

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Instructions: Consider the data below to answer the following question(s). Cyanohydrins are important intermediates in the synthesis of a-hydroxycarboxylic acids from ketones and aldehydes.The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid.Nitriles can also be hydrolyzed to carboxylic acids using aqueous base.When a cyanohydrin is treated with aqueous base,however,the original carbonyl compound is isolated. Instructions: Consider the data below to answer the following question(s). Cyanohydrins are important intermediates in the synthesis of a-hydroxycarboxylic acids from ketones and aldehydes.The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid.Nitriles can also be hydrolyzed to carboxylic acids using aqueous base.When a cyanohydrin is treated with aqueous base,however,the original carbonyl compound is isolated.     -Refer to instructions.Identify the electrophile and nucloephile in the reaction of benzaldehyde with hydrogen cyanide. -Refer to instructions.Identify the electrophile and nucloephile in the reaction of benzaldehyde with hydrogen cyanide.

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What is the name of the major organic product obtained from the following reaction? What is the name of the major organic product obtained from the following reaction?

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Instructions: a,b-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the b carbon,as shown below.Use this information to answer the following question(s). Instructions: a,b-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the b carbon,as shown below.Use this information to answer the following question(s).    -Refer to instructions.This reaction is called a(n)_____ reaction. -Refer to instructions.This reaction is called a(n)_____ reaction.

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Many nucleophilic addition reactions of aldehydes and ketones are catalyzed by acid or base.Bases catalyze hydration by:

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound?

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Instructions: Consider the data below to answer the following question(s). Cyanohydrins are important intermediates in the synthesis of a-hydroxycarboxylic acids from ketones and aldehydes.The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid.Nitriles can also be hydrolyzed to carboxylic acids using aqueous base.When a cyanohydrin is treated with aqueous base,however,the original carbonyl compound is isolated. Instructions: Consider the data below to answer the following question(s). Cyanohydrins are important intermediates in the synthesis of a-hydroxycarboxylic acids from ketones and aldehydes.The nitrile functional group can be hydrolyzed by aqueous acid to yield a carboxylic acid.Nitriles can also be hydrolyzed to carboxylic acids using aqueous base.When a cyanohydrin is treated with aqueous base,however,the original carbonyl compound is isolated.    -Refer to instructions.The reaction of an aldehyde with hydrogen cyanide is an example of _____ reaction. -Refer to instructions.The reaction of an aldehyde with hydrogen cyanide is an example of _____ reaction.

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In the box,what is the name of the reactant used in the following reaction? In the box,what is the name of the reactant used in the following reaction?

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Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a phosphorus ylide.Synthesize the following alkene through the Wittig reaction of a carbonyl compound and a phosphorus ylide.

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Draw the structure of the product obtained from the following reaction.Draw the structure of the product obtained from the following reaction.

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Instructions: Consider the data below to answer the following question(s). C7H14O Instructions: Consider the data below to answer the following question(s). C<sub>7</sub>H<sub>14</sub>O     -Refer to instructions.Propose a structure consistent with the spectral data presented above. -Refer to instructions.Propose a structure consistent with the spectral data presented above.

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The nucleophillic addition of water to an aldehyde or ketone

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Predict whether the following reactions of the depicted carbonyl containing compounds and amines will result in the formation of an enamine or an imine. Predict whether the following reactions of the depicted carbonyl containing compounds and amines will result in the formation of an enamine or an imine.

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

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Instructions: Consider the data below to answer the following question(s). C7H14O Instructions: Consider the data below to answer the following question(s). C<sub>7</sub>H<sub>14</sub>O     -Refer to instructions.Calculate the degree of unsaturation for this compound. -Refer to instructions.Calculate the degree of unsaturation for this compound.

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The substance formed in the following reaction is called: The substance formed in the following reaction is called:

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