Exam 9: Aldehydes and Ketones: Nucleophilic Addition Reactions
Exam 1: Structure and Bonding:acids and Bases40 Questions
Exam 2: Alkanes: The Nature of Organic Compounds47 Questions
Exam 3: Alkenes and Alkynes: the Nature of Organic Reactions37 Questions
Exam 4: Reactions of Alkenes and Alkynes44 Questions
Exam 5: Aromatic Compounds51 Questions
Exam 6: Sterechemistry at Tetrahedral Centers35 Questions
Exam 7: Organohalides: Nucleophilic Substitutions and Eliminations49 Questions
Exam 8: Alcohols, Phenols, Ethers, and Their Sulfur Analogs39 Questions
Exam 9: Aldehydes and Ketones: Nucleophilic Addition Reactions32 Questions
Exam 10: Carboxylic Acids and Derivatives: Nucleophilic Acyl Substitution Reactions66 Questions
Exam 11: Carbonyl Alpha-Substitution Reactions and Condensation Reactions37 Questions
Exam 12: Amines31 Questions
Exam 13: Structure Determination64 Questions
Exam 14: Biomolecules: Carbohydrates41 Questions
Exam 15: Biomolecules: Amino Acids, Peptides, and Proteins43 Questions
Exam 16: Biomolecules: Lipids and Nucleic Acids37 Questions
Exam 17: The Organic Chemistry of Metabolic Pathways35 Questions
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Instructions: Consider the reaction below to answer the following question.
Refer to instructions. The electrophile, the nucleophile and the catalyst in this reaction are indicated by letters _____, _____, and _____, respectively.

Free
(Short Answer)
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Correct Answer:
A, B and C
The substance formed in the following reaction is called: 

Free
(Multiple Choice)
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Correct Answer:
E
Many nucleophilic addition reactions of aldehydes and ketones are catalyzed by acid or base. Bases catalyze hydration by:
(Multiple Choice)
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Instructions: Consider the reaction below to answer the following question.
Refer to instructions. Write the complete stepwise mechanism for the reaction shown above. Show all intermediate structures and all electron flow with arrows.

(Essay)
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Draw structures corresponding to each of the following names.
Draw:
5,5-dimethylcyclohexane-1,3-dione (dimedone)
(Essay)
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Instructions: Predict the products from the information given for the following question(s).
Predict: 

(Essay)
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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.
Refer to instructions. The reaction of an aldehyde with hydrogen cyanide is an example of _____ reaction.

(Multiple Choice)
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Draw structures corresponding to each of the following names.
Draw:
2,2-dimethylcyclopentane-1,3-dione
(Essay)
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The nucleophillic addition of water to an aldehyde or ketone
(Multiple Choice)
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Instructions: Consider the reaction below to answer the following question.
Refer to instructions. The product of this reaction is called:

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

(Essay)
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Outline the synthetic steps necessary to carry out the conversion below. You may use any organic or inorganic reagents you need. Show the structures of all intermediate compounds that would probably be isolated during the course of your synthesis, and show all necessary reagents 

(Essay)
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Draw structures corresponding to each of the following names.
Draw:
cyclohex-2-enone
(Essay)
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Draw structures corresponding to each of the following names.
Draw:
benzophenone
(Essay)
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Draw structures corresponding to each of the following names.
Draw:
trans-3-isopropylcyclohexanecarbaldehyde
(Essay)
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