ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI
ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI
6th Edition
ISBN: 9781319306946
Author: LOUDON
Publisher: MAC HIGHER
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 19, Problem 19.41AP
Interpretation Introduction

(a)

Interpretation:

The product formed in the reaction of butyraldehyde and PhMgBr, then with dilute H3O+ is to be predicted.

Concept introduction:

Grignard reagents are organometallic compounds which are prepared using alkyl halides in the presence of magnesium metal in dry ether. These reagents act as strong nucleophiles and bases. The Grignard reagent is used to increase the chain length of the carbon-carbon bond.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and PhMgBr, then with dilute H3O+ is an alcohol as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  1

Explanation of Solution

Butyraldehyde reacts with PhMgBr, then with dilute H3O+ to give 1-phenylbutan-1-ol. The product formed in this reaction is by the help of Grignard reagent.

The reduction of butyraldehyde takes place to form the product. The reaction is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  2

Figure 1

Conclusion

The product formed in the reaction of butyraldehyde and PhMgBr, then with dilute H3O+ is 1-phenylbutan-1-ol as shown in Figure 1.

Interpretation Introduction

(b)

Interpretation:

The product formed in the reaction of butyraldehyde and LiAlH4 in ether, then with dilute H3O+ is to be predicted.

Concept introduction:

The gain of electrons involved in the particular reaction is termed as reduction. The reduction process also involves the removal of an electronegative atom from a molecule followed by the hydrogen atom addition into that molecule.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and LiAlH4 in ether, then with dilute H3O+ is an alcohol as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  3

Explanation of Solution

Butyraldehyde reacts with LiAlH4, then with dilute H3O+ to give butan-1-ol. The product formed in this reaction is by the help of lithium aluminium hydride.

The reduction of butyraldehyde takes place to form the product. The reaction is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  4

Figure 2

Conclusion

The product formed in the reaction of butyraldehyde and LiAlH4, then with dilute H3O+ is butan-1-ol as shown in Figure 2.

Interpretation Introduction

(c)

Interpretation:

The product formed in the reaction of butyraldehyde and alkaline KMnO4, then with dilute H3O+ is to be predicted.

Concept introduction:

Oxidation is the process of addition of oxygen. Oxidation is also defined as loss of electrons. In the oxidation process, there is increase in the oxidation state. The acid is added in the reaction for protonation.

The oxidizing agent is defined as the species which oxidizes others and itself gets reduced.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and KMnO4, then with dilute H3O+ is a butyric acid as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  5

Explanation of Solution

Butyraldehyde reacts with KMnO4, then with dilute H3O+ to give butyric acid. The alkaline KMnO4 is used to oxidize aldehyde into their respective acid. The hydronium ion is used for protonation in the reaction which is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  6

Figure 3

Conclusion

The product formed in the reaction of butyraldehyde and alkaline KMnO4, then with dilute H3O+ is butyric acid as shown in Figure 3.

Interpretation Introduction

(d)

Interpretation:

The product formed in the reaction of butyraldehyde and aqueous H2Cr2O7 is to be predicted.

Concept introduction:

Oxidation is the process of addition of oxygen. Oxidation is also defined as loss of electrons. In the oxidation process, there is increase in the oxidation state. The acid is added in the reaction for protonation.

The oxidizing agent is defined as the species which oxidizes others and itself gets reduced.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and aqueous H2Cr2O7 is a butyric acid as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  7

Explanation of Solution

Butyraldehyde reacts with aqueous H2Cr2O7 to give butyric acid.. The aqueous H2Cr2O7 is used to oxidize aldehyde into their respective acid. The hydronium ion is used for protonation in the reaction which is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  8

Figure 4

Conclusion

The product formed in the reaction of butyraldehyde and aqueous H2Cr2O7 is butyric acid as shown in Figure 4.

Interpretation Introduction

(e)

Interpretation:

The product formed in the reaction of butyraldehyde and NH2OH at pH=5 is to be predicted.

Concept introduction:

Oxime belongs to the family of imines. The formula of oxime is RR'C=NOH. Types of oxime are ketoxime and aldoxime. This reaction proceeds through a nucleophilic addition reaction. The catalyst acts as a nucleophile in the reaction.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and NH2OH at pH=5 is a butyraldehyde oxime as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  9

Explanation of Solution

Butyraldehyde reacts with NH2OH at pH=5 to give butyraldehyde oxime. The NH2OH is used to convert aldehyde into aldehyde oxime. This reaction is based on the importance of ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  10. When the ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  11is high then the product formed is an amine. However, when the ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  12is low then the product is not formed. The reaction is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  13

Figure 5

Conclusion

The product formed in the reaction of butyraldehyde and NH2OH at pH=5 is butyraldehyde oxime as shown in Figure 5.

Interpretation Introduction

(f)

Interpretation:

The product formed in the reaction of butyraldehyde and Ag2O is to be predicted.

Concept introduction:

Oxidation is the process of addition of oxygen. Oxidation is also defined as loss of electrons. In the oxidation process, there is increase in the oxidation state. The acid is added in the reaction for protonation.

The oxidizing agent is defined as the species which oxidizes others and itself gets reduced.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and Ag2O is a butyric acid as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  14

Explanation of Solution

Butyraldehyde reacts with Ag2O to give butyric acid. The Ag2O is used to oxidize aldehyde into their respective acid. The OH acts as a nucleophile which attacks on the carbonyl carbon of the aldehyde.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  15

Figure 6

Conclusion

The product formed in the reaction of butyraldehyde and Ag2O is a butyric acid as shown in Figure 6.

Interpretation Introduction

(g)

Interpretation:

The product formed in the reaction of butyraldehyde and zinc amalgam in the presence of HCl is to be predicted.

Concept introduction:

Clemmensen reduction is defined as the reduction in which aldehydes or ketones are converted into alkane or hydrocarbon. The catalyst is used in this reaction is zinc amalgam in the presence of concentrated hydrochloric acid. This is one of the easy methods to convert aldehydes or ketones into hydrocarbon.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The product formed in the reaction of butyraldehyde and zinc amalgam in the presence of HCl is butane as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  16

Explanation of Solution

Butyraldehyde reacts with zinc amalgam in the presence of HCl to give butane. Zinc is oxidized and the losing electrons are attracted by carbonyl carbon. Then protonation takes place and carbocation is formed. Carbocation taking two electrons and neutralized by acid. The overall reaction is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  17

Figure 7

Conclusion

The product formed in the reaction of butyraldehyde and zinc amalgam in the presence of HCl is butane as shown in Figure 7.

Interpretation Introduction

(h)

Interpretation:

The product formed in the reaction of butyraldehyde and CH3CH=PPh3 is to be predicted.

Concept introduction:

The Wittig reaction is the chemical reaction that involves conversion of an aldehyde or ketone into an alkene. The chemical name of Wittig reagent is triphenyl phosphonium ylide. In the Wittig reaction, aldehydes or a ketone reacts with triphenyl phosphonium ylide to generate an alkene and triphenylphosphine oxide. The Wittig reagent gives good yields of alkene even when other functional groups are present on the aldehydes or ketone. However, as the steric hindrance of the aldehydes or ketone increases, the yield of alkene decreases.

Expert Solution
Check Mark

Answer to Problem 19.41AP

The geometrical isomers are formed in the reaction of butyraldehyde and CH3CH=PPh3 as shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  18

Explanation of Solution

Butyraldehyde reacts with CH3CH=PPh3 forms two geometrical isomeric units. When the butyraldehyde is treated with ylide. The conjugate base of the phosphonium ion leads to the formation of the product. The double bond of the carbonyl bond is converted into an alkene. The cis and trans geometrical isomers are obtained. The reaction is shown below.

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI, Chapter 19, Problem 19.41AP , additional homework tip  19

Figure 8

Conclusion

Butyraldehyde reacts with CH3CH=PPh3 forms two geometrical isomeric units as shown in Figure 8.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Define the Mechanism - Conversion of Carboxylic Acids to Amides with DCC
Isoprene has sometimes been used as a starting material in the laboratory synthesis of terpenes. In one such synthesis, the first step is the electrophilic addition of 2 mol of hydrogen bromide to isoprene to give 1,3-dibromo-3-methylbutane.Write a series of equations describing the mechanism of this reaction.
The treatment of (CH3)2C=CHCH2Br with H2O forms B (molecular formulaC5H10O) as one of the products. Determine the structure of B from its 1H NMR and IR spectra.

Chapter 19 Solutions

ORGANIC CHEMISTRY (LL)+ SAPLING ACC >BI

Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Characteristic Reactions of Benzene and Phenols; Author: Linda Hanson;https://www.youtube.com/watch?v=tjEqEjDd87E;License: Standard YouTube License, CC-BY
An Overview of Aldehydes and Ketones: Crash Course Organic Chemistry #27; Author: Crash Course;https://www.youtube.com/watch?v=-fBPX-4kFlw;License: Standard Youtube License