In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated. Concept Introduction: Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions. Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Question

Want to see the full answer?

Answer 1

Question

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

The hydrolysis of an amide in acidic conditions forms A. a carboxylate salt and an alcohol B. a carboxylate salt and an amine C. an alcohol and an amine salt (an ammonium ion) D. a carboxylic acid and an amine salt (an ammonium ion)

why Acetanilide at room temperature is less soluble?

When comparing the structures of aspirin and acetaminophen, why can acetaminophen exist in a liquid state (i.e. childrens drinkable tylenol) and aspirin cannot? Does it have to do with the carboxylic acid? The question says that liquid aspirin cannot be made. Why would that be?

Answer 2

Question

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 6

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 7

Chapter 17, Problem 17.124EP

(a)

Interpretation Introduction

Interpretation:

In aqueous solution, methylethylamine exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 8

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 9

(b)

Interpretation Introduction

Interpretation:

In aqueous solution, butanamide exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 10

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 11

(c)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 12

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 13

(d)

Interpretation Introduction

Interpretation:

In aqueous solution, the given compound exhibit basic behavior or not has to be indicated.

Concept Introduction:

Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.

Amides have a carbonyl group bonded to the nitrogen atom. The carbonyl carbon atom pulls the lone pair of electrons present on the nitrogen strongly. Hence, the nitrogen atom cannot act as a proton acceptor. Amides are not basic in nature.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 17.1 - Prob. 1QQ Ch. 17.1 - Prob. 2QQ Ch. 17.2 - Prob. 1QQ Ch. 17.2 - Prob. 2QQ Ch. 17.2 - Prob. 3QQ Ch. 17.2 - Prob. 4QQ Ch. 17.3 - Prob. 1QQ Ch. 17.3 - Prob. 2QQ Ch. 17.3 - Prob. 3QQ Ch. 17.3 - Prob. 4QQ

Solution Summary: The author explains that methylethylamine exhibits basic behavior or not in aqueous solutions.

Want to see the full answer?

Chapter 17 Solutions