Structure of optically inactive triglyceride need to be drawn from the given glycerol, one equivalent of palmitic acid and two equivalents of myristic acid and also to check whether the formed triglyceride will react with molecular hydrogen. Concept introduction: Esterification is a process in which the carboxylic acid and an alcohol react to form a ester bond. This can take place in presence of acid or base. The bond is formed due to loss of water molecule when the condensation reaction takes place. Simply to say esterification is the reverse process of hydrolysis. From the above scheme we can find out the starting triglyceride considering the fatty acid and glycerol. Molecular hydrogen will react with unsaturated compounds to reduce them. If the compound does not have any unsaturation then that compound wont react with molecular hydrogen. To draw: the structure of optically active triglyceride from the given problem statement.

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 26, Problem 32PP

Interpretation Introduction

Interpretation:

Structure of optically inactive triglyceride need to be drawn from the given glycerol, one equivalent of palmitic acid and two equivalents of myristic acid and also to check whether the formed triglyceride will react with molecular hydrogen.

Concept introduction:

Esterification is a process in which the carboxylic acid and an alcohol react to form a ester bond. This can take place in presence of acid or base. The bond is formed due to loss of water molecule when the condensation reaction takes place. Simply to say esterification is the reverse process of hydrolysis.

From the above scheme we can find out the starting triglyceride considering the fatty acid and glycerol.

Molecular hydrogen will react with unsaturated compounds to reduce them. If the compound does not have any unsaturation then that compound wont react with molecular hydrogen.

To draw: the structure of optically active triglyceride from the given problem statement.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Please help me solve this reaction.

Indicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.

Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.

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 26, Problem 32PP

Interpretation Introduction

Interpretation:

Structure of optically inactive triglyceride need to be drawn from the given glycerol, one equivalent of palmitic acid and two equivalents of myristic acid and also to check whether the formed triglyceride will react with molecular hydrogen.

Concept introduction:

Esterification is a process in which the carboxylic acid and an alcohol react to form a ester bond. This can take place in presence of acid or base. The bond is formed due to loss of water molecule when the condensation reaction takes place. Simply to say esterification is the reverse process of hydrolysis.

From the above scheme we can find out the starting triglyceride considering the fatty acid and glycerol.

Molecular hydrogen will react with unsaturated compounds to reduce them. If the compound does not have any unsaturation then that compound wont react with molecular hydrogen.

To draw: the structure of optically active triglyceride from the given problem statement.

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 26, Problem 32PP

Interpretation Introduction

Interpretation:

Structure of optically inactive triglyceride need to be drawn from the given glycerol, one equivalent of palmitic acid and two equivalents of myristic acid and also to check whether the formed triglyceride will react with molecular hydrogen.

Concept introduction:

Esterification is a process in which the carboxylic acid and an alcohol react to form a ester bond. This can take place in presence of acid or base. The bond is formed due to loss of water molecule when the condensation reaction takes place. Simply to say esterification is the reverse process of hydrolysis.

From the above scheme we can find out the starting triglyceride considering the fatty acid and glycerol.

Molecular hydrogen will react with unsaturated compounds to reduce them. If the compound does not have any unsaturation then that compound wont react with molecular hydrogen.

To draw: the structure of optically active triglyceride from the given problem statement.

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 26, Problem 32PP

Interpretation Introduction