Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
Chapter 22.7, Problem 10P
Interpretation Introduction

a)

Interpretation:

The most acidic hydrogen in molecule CH3CH2CHO is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To give the most acidic hydrogen in molecule of CH3CH2CHO.

Interpretation Introduction

b)

Interpretation:

The most acidic hydrogen in molecule (CH3)3CCOCH is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To give the most acidic hydrogen in molecule of (CH3)3CCOCH.

Interpretation Introduction

c)

Interpretation:

The most acidic hydrogen in molecule CH3CO2H is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To give the most acidic hydrogen in molecule of CH3CO2H.

Interpretation Introduction

d)

Interpretation:

The most acidic hydrogen in Benzamide is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To give the most acidic hydrogen in Benzamide.

Interpretation Introduction

e)

Interpretation:

The most acidic hydrogen in a molecule CH3CH2CH2CN is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To identify the most acidic hydrogen in a molecule CH3CH2CH2CN.

Interpretation Introduction

f)

Interpretation:

The most acidic hydrogen in a molecule CH3CON(CH3)2 is to be given.

Concept introduction:

Hydrogen’s on carbon next to a carbonyl group are acidic. In general, α β dicarbonyl compounds is most acidic, a ketone or aldehyde is next acidic and a carboxylic acid derivative is least acidic. Alcohols, phenols and carboxylic acid are also acidic because of their –OH hydrogen’s.

To give:

To identify the most acidic hydrogen in a molecule CH3CON(CH3)2.

Blurred answer
Students have asked these similar questions
Show work with explanation needed. don't give Ai generated solution
Show work. don't give Ai generated solution
None

Chapter 22 Solutions

Organic Chemistry

Ch. 22.7 - Draw a resonance structure of the acetonitrile...Ch. 22.7 - Why do you suppose ketone halogenations in acidic...Ch. 22.7 - Prob. 13PCh. 22.7 - Prob. 14PCh. 22.7 - Prob. 15PCh. 22.7 - Prob. 16PCh. 22.SE - Prob. 17VCCh. 22.SE - Prob. 18VCCh. 22.SE - Prob. 19VCCh. 22.SE - Prob. 20MPCh. 22.SE - Predict the product(s) and provide the mechanism...Ch. 22.SE - Predict the product(s) and provide the mechanism...Ch. 22.SE - Prob. 23MPCh. 22.SE - In the Hell–Volhard–Zelinskii reaction, only a...Ch. 22.SE - Prob. 25MPCh. 22.SE - Nonconjugated , -unsaturated ketones, such as...Ch. 22.SE - Prob. 27MPCh. 22.SE - Using curved arrows, propose a mechanism for the...Ch. 22.SE - Prob. 29MPCh. 22.SE - One of the later steps in glucose biosynthesis is...Ch. 22.SE - The Favorskii reaction involves treatment of an...Ch. 22.SE - Treatment of a cyclic ketone with diazomethane is...Ch. 22.SE - Prob. 33MPCh. 22.SE - Amino acids can be prepared by reaction of alkyl...Ch. 22.SE - Amino acids can also be prepared by a two-step...Ch. 22.SE - Heating carvone with aqueous sulfuric acid...Ch. 22.SE - Identify all the acidic hydrogens (pKa 25) in the...Ch. 22.SE - Rank the following compounds in order of...Ch. 22.SE - Prob. 39APCh. 22.SE - Base treatment of the following , -unsaturated...Ch. 22.SE - Prob. 41APCh. 22.SE - Prob. 42APCh. 22.SE - Prob. 43APCh. 22.SE - Which, if any, of the following compounds can be...Ch. 22.SE - Prob. 45APCh. 22.SE - Prob. 46APCh. 22.SE - Prob. 47APCh. 22.SE - How might you convert geraniol into either ethyl...Ch. 22.SE - Prob. 49APCh. 22.SE - One way to determine the number of acidic...Ch. 22.SE - Prob. 51APCh. 22.SE - Prob. 52APCh. 22.SE - Prob. 53APCh. 22.SE - Prob. 54APCh. 22.SE - Prob. 55APCh. 22.SE - Prob. 56APCh. 22.SE - All attempts to isolate primary and secondary...Ch. 22.SE - How would you synthesize the following compounds...Ch. 22.SE - Prob. 59APCh. 22.SE - Prob. 60APCh. 22.SE - Prob. 61APCh. 22.SE - Prob. 62APCh. 22.SE - As far back as the 16th century, South American...Ch. 22.SE - The key step in a reported laboratory synthesis of...Ch. 22.SE - Prob. 65AP
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.
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:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning