Question 1

Predict the product(s) for the following reaction.

Accepted Answer

The answer of Predict the product(s) for the following reaction....

Question 2

Predict the product for the following reaction.

Accepted Answer

The answer of Predict the product for the following reaction....

Question 3

Provide the reagents necessary to carry out the following conversion.

Accepted Answer

A)  1. CH3Cl/AlCl3
2) Br2/h$v$
3) NaCN 
B)  1. CH3Cl/AlCl3
2) HCN 
C)  1. Br2/FeBr3
2) Mg/ether
3) CO2
4) H3O+
5) SOCl2
6) excess NH3
7) SOCl2 
D)  A and C 
E)  A and B 
A)  1. CH3Cl/AlCl3
2) Br2/h$v$
3) NaCN 
B)  1. CH3Cl/AlCl3
2) HCN 
C)  1. Br2/FeBr3
2) Mg/ether
3) CO2
4) H3O+
5) SOCl2
6) excess NH3
7) SOCl2 
D)  A and C 
E)  A and B

Question 4

Predict the product for the following reaction.

Accepted Answer

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

Question 5

Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion.

Accepted Answer

@#IMG-DLM&_TB4454_00

Question 6

Provide the reagents necessary to carry out the following conversion.

Accepted Answer

1. Mg/ether 2. H₂C=O

Question 7

Which one of the following compounds has the highest boiling point?

Accepted Answer

A)  butanoic acid 
B)  1-butanol 
C)  2-butanone 
D)  methoxyethane 
E)  butanal 
A)  butanoic acid 
B)  1-butanol 
C)  2-butanone 
D)  methoxyethane 
E)  butanal

Question 8

Which one of the following is the strongest acid?

Accepted Answer

A)  2,2-dichlorobutanoic acid 
B)  2,3-dichlorobutanoic acid 
C)  3,3-dichlorobutanoic acid 
D)  3,4-dichlorobutanoic acid 
E)  4,4-dichlorobutanoic acid 
A)  2,2-dichlorobutanoic acid 
B)  2,3-dichlorobutanoic acid 
C)  3,3-dichlorobutanoic acid 
D)  3,4-dichlorobutanoic acid 
E)  4,4-dichlorobutanoic acid

Question 9

What is the IUPAC name for the following compound?

Accepted Answer

A)  methanoic anhydride 
B)  ethanoic anhydride 
C)  acetic anhydride 
D)  formic anhydride 
E)  propanoic anhydride 
A)  methanoic anhydride 
B)  ethanoic anhydride 
C)  acetic anhydride 
D)  formic anhydride 
E)  propanoic anhydride

Question 10

Which one of the following compounds has the highest boiling point?

Accepted Answer

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

Question 11

What is the IUPAC name for the following compound?

Accepted Answer

A)  3-fluorobutanoic acid 
B)  2-fluorobutanoic acid 
C)  β-fluorobutyric acid 
D)  α-fluorobutyric acid 
E)  none of these 
A)  3-fluorobutanoic acid 
B)  2-fluorobutanoic acid 
C)  β-fluorobutyric acid 
D)  α-fluorobutyric acid 
E)  none of these

Question 12

What is the IUPAC name for the following compound?

Accepted Answer

N,N-diethy

Question 13

Predict the product for the following reaction.

Accepted Answer

A)  ethyl 3-methylbutanoate 
B)  ethyl 2-methylpropanoate 
C)  isobutyl ethanoate 
D)  5-methyl-3-hexanone 
E)  none of these 
A)  ethyl 3-methylbutanoate 
B)  ethyl 2-methylpropanoate 
C)  isobutyl ethanoate 
D)  5-methyl-3-hexanone 
E)  none of these

Question 14

What is the common name for the following compound?

Accepted Answer

A)  ($\alpha$-bromoacetyl bromide) 
B)  ($\beta$-bromoacetyl bromide) 
C)  1-bromoethanoyl bromide 
D)  2-bromoethanoyl bromide 
E)  1,2-dibromoacetic acid 
A)  ($\alpha$-bromoacetyl bromide) 
B)  ($\beta$-bromoacetyl bromide) 
C)  1-bromoethanoyl bromide 
D)  2-bromoethanoyl bromide 
E)  1,2-dibromoacetic acid

Question 15

Which of the following is the weakest acid?

Accepted Answer

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

Question 16

What is the IUPAC name for the following compound?

Accepted Answer

A)  propanoic anhydride 
B)  butanoic anhydride 
C)  propionic anhydride 
D)  pentanoic anhydride 
E)  butyric anhydride 
A)  propanoic anhydride 
B)  butanoic anhydride 
C)  propionic anhydride 
D)  pentanoic anhydride 
E)  butyric anhydride

Question 17

Provide the reagents necessary to carry out the following conversion.

Accepted Answer

The answer of Provide the reagents necessary to carry out...

Question 18

Provide the structure for 5-chloro-3-isopropyloctanoic acid.

Accepted Answer

The answer of Provide the structure for 5-chloro-3-isopropyloctanoic acid....

Question 19

Provide the reagents necessary to carry out the following conversion.

Accepted Answer

1. Cl₂/FeCl

Question 20

What is the correct structure for trichloroacetic acid?

Accepted Answer

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

Exam 20: Carboxylic Acids and Their Derivatives

Predict the product(s) for the following reaction.

Predict the product for the following reaction.

Provide the reagents necessary to carry out the following conversion.

Predict the product for the following reaction.

Using ethyl 3-methylbutanoate as your only source of carbon and using any other reagents necessary, propose a stepwise synthesis for the following conversion.

Provide the reagents necessary to carry out the following conversion.

Which one of the following compounds has the highest boiling point?

Which one of the following is the strongest acid?

What is the IUPAC name for the following compound?

Which one of the following compounds has the highest boiling point?

What is the IUPAC name for the following compound?

What is the IUPAC name for the following compound?

Predict the product for the following reaction.

What is the common name for the following compound?

Which of the following is the weakest acid?

What is the IUPAC name for the following compound?

Provide the reagents necessary to carry out the following conversion.

Provide the structure for 5-chloro-3-isopropyloctanoic acid.

Provide the reagents necessary to carry out the following conversion.

What is the correct structure for trichloroacetic acid?

A Review of General Chemistry: Electrons, Bonds, and Molecular Properties

Molecular Representations

Acids and Bases

Alkanes and Cycloalkanes

Stereoisomerism

Chemical Reactivity and Mechanisms

Alkyl Halides: Nucleophilic Substitution and Elimination Reactions

Addition Reactions of Alkenes

Alkynes

Radical Reactions

Synthesis

Alcohols and Phenols

Ethers and Epoxides; Thiols and Sulfides

Infrared Spectroscopy and Mass Spectrometry

Nuclear Magnetic Resonance Spectroscopy

Conjugated Pi Systems and Pericyclic Reactions

Aromatic Compounds

Aromatic Substitution Reactions

Aldehydes and Ketones

Alpha Carbon Chemistry: Enols and Enolates

Amines

Introduction to Organometallic Compounds

Carbohydrates

Amino Acids, Peptides, and Proteins

Lipids

Synthetic Polymers

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