Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions
Exam 1: Structure and Bonding30 Questions
Exam 2: Polar Covalent Bonds: Acids and Bases35 Questions
Exam 3: Organic Compounds: Alkanes and Their Stereochemistry32 Questions
Exam 4: Organic Compounds: Cycloalkanes and Their Stereochemistry18 Questions
Exam 5: Stereochemistry at Tetrahedral Centers33 Questions
Exam 6: An Overview of Organic Reactions32 Questions
Exam 7: Alkenes and Alkynes34 Questions
Exam 8: Reactions of Alkenes and Alkynes37 Questions
Exam 9: Aromatic Compounds36 Questions
Exam 10: Structure Determination: Mass Spectrometry,infrared Spectroscopy,and Ultraviolet Spectroscopy41 Questions
Exam 11: Structure Determination: Nuclear Magnetic Resonance Spectroscopy37 Questions
Exam 12: Organohalides: Nucleophilic Substitutions and Eliminations37 Questions
Exam 13: Alcohols,phenols,and Thiols: Ethers and Sulfides19 Questions
Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions30 Questions
Exam 15: Carboxylic Acids and Nitriles23 Questions
Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions42 Questions
Exam 17: Carbonyl Alpha-Substitution and Condensation Reactions84 Questions
Exam 18: Amines and Heterocycles28 Questions
Exam 19: Biomolecules: Amino Acids,peptides,and Proteins36 Questions
Exam 20: Amino Acid Metabolism34 Questions
Exam 21: Biomolecules: Carbohydrates42 Questions
Exam 22: Carbohydrate Metabolism41 Questions
Exam 23: Biomolecules: Lipids and Their Metabolism31 Questions
Exam 24: Biomolecules: Nucleic Acids and Their Metabolism23 Questions
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What is the major organic product produced by the following reaction?

(Essay)
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Instructions: Provide the missing structure(s)or reagent(s)for each reaction or sequences of reactions.Show all relevant stereochemistry.
-Provide missing structure(s):

(Essay)
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Instructions: Provide the missing structure(s)or reagent(s)for each reaction or sequences of reactions.Show all relevant stereochemistry.
-Provide missing structure(s):

(Essay)
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Instructions: Consider the reaction below to answer the following question(s).
-Refer to instructions.Write the complete stepwise mechanism for this reaction.Show intermediate structures and all electron flow with arrows.

(Essay)
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Instructions: Provide the missing structure(s)or reagent(s)for each reaction or sequences of reactions.Show all relevant stereochemistry.
-Provide missing structure(s):

(Essay)
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Instructions: Consider the information below to answer the following question(s).
The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification.
-Refer to instructions.The nucleophile in this reaction is indicated by letter _____.

(Multiple Choice)
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Which of the following best describes the key mechanistic steps in the reaction of an acid chloride and an alcohol to form an ester?
(Multiple Choice)
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Instructions: Tell which spectroscopic technique you would use to distinguish between the two members of the pair.Tell what differences you would expect to see.
-Identify spectroscopic technique:

(Essay)
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Of the following,which represents a possible direct conversion of the reactant to product shown?
(Multiple Choice)
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The two spectra below belong to acetic acid (ethanoic acid)and its isomer,methyl formate (methyl methanoate).Which spectrum corresponds to which compound? Explain your answer.
(Spectra obtained from SDBSWeb:http://www.aist.go.jp/RIODB/SDBS)


(Essay)
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Which of the following is the correct assignment of the classes of the following compounds? 

(Multiple Choice)
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Draw the major product of the following reaction (which affords a penicillin derivative).

(Essay)
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Instructions: Consider the information below to answer the following question(s).
The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification.
-Refer to instructions.What would be the identity of A,B and C needed to produce the following compound?


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Instructions: Consider the reaction below to answer the following question(s).
-Refer to instructions.This reaction is an example of:

(Multiple Choice)
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The following a monomer of the polymer used in biodegradable sutures called Lactomerâ.Upon hydrolysis what product(s)form(s)? Draw the appropriate structure(s).

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Rank the following from highest to lowest reactivity toward reaction with EtOH.

(Essay)
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Instructions: Consider the reaction below to answer the following question(s).
-Refer to instructions.The purpose of the base catalyst in this reaction is:

(Multiple Choice)
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Instructions: Consider the information below to answer the following question(s).
The reaction of a carboxylic acid with an alcohol in the presence of acid is termed a Fischer esterification.
-Refer to instructions.Compound C functions as _____ in this reaction.

(Multiple Choice)
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