The reason for insolubility of amino acids in diethyl ether unlike most of the amines and carboxylic acids has to be explained. Concept introduction: Polar compound soluble in polar solvents and non-polar compounds dissolves in non-polar solvents (like dissolves like). Amino acids exist as zwitterion at certain p H , in which the amount of positive charge and negative charge on an amino acid becomes balanced. Zwitter ion: Zwitter ion has both positive as well as negative charge, thus it is also called neutral dipolar ion. Zwitter ion accepts proton in acidic condition and in basic condition zwitter ion lose electrons. Example: Zwitter ion

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 17.3, Problem 3P

Interpretation Introduction

Interpretation:

The reason for insolubility of amino acids in diethyl ether unlike most of the amines and carboxylic acids has to be explained.

Concept introduction:

Polar compound soluble in polar solvents and non-polar compounds dissolves in non-polar solvents (like dissolves like).

Amino acids exist as zwitterion at certain pH, in which the amount of positive charge and negative charge on an amino acid becomes balanced.

Zwitter ion: Zwitter ion has both positive as well as negative charge, thus it is also called neutral dipolar ion.

Zwitter ion accepts proton in acidic condition and in basic condition zwitter ion lose electrons.

Example: Zwitter ion

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

General reactions for drugs belonging to the group of aliphatic amino acids: A) with iodine solution B) With ninhydrin C) With copper sulfate in an alkaline environment D) With resorcinol

α-Amino acids can be prepared by treating an aldehyde with ammonia/trace acid, followed by hydrogen cyanide, followed by acid-catalyzed hydrolysis. What amino acid is formed when the aldehyde that is used is 3-methylbutanal?

α-Amino acids can be prepared by treating an aldehyde with ammonia/trace acid, followed by hydrogen cyanide, followed by acid-catalyzed hydrolysis. What aldehyde is needed to prepare isoleucine?

Answer 2

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 17.3, Problem 3P

Interpretation Introduction

Interpretation:

The reason for insolubility of amino acids in diethyl ether unlike most of the amines and carboxylic acids has to be explained.

Concept introduction:

Polar compound soluble in polar solvents and non-polar compounds dissolves in non-polar solvents (like dissolves like).

Amino acids exist as zwitterion at certain pH, in which the amount of positive charge and negative charge on an amino acid becomes balanced.

Zwitter ion: Zwitter ion has both positive as well as negative charge, thus it is also called neutral dipolar ion.

Zwitter ion accepts proton in acidic condition and in basic condition zwitter ion lose electrons.

Example: Zwitter ion

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 17.3, Problem 3P

Interpretation Introduction

Interpretation:

The reason for insolubility of amino acids in diethyl ether unlike most of the amines and carboxylic acids has to be explained.

Concept introduction:

Polar compound soluble in polar solvents and non-polar compounds dissolves in non-polar solvents (like dissolves like).

Amino acids exist as zwitterion at certain pH, in which the amount of positive charge and negative charge on an amino acid becomes balanced.

Zwitter ion: Zwitter ion has both positive as well as negative charge, thus it is also called neutral dipolar ion.

Zwitter ion accepts proton in acidic condition and in basic condition zwitter ion lose electrons.

Example: Zwitter ion

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 17.3, Problem 3P

Interpretation Introduction