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.

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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.

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Students have asked these similar questions

1. Show the steps necessary to make 2-methyl-4-nonene using a Wittig reaction. Start with triphenylphosphine and an alkyl halide. After that you may use any other organic or inorganic reagents. 2. Write in the product of this reaction: CH3 CH₂ (C6H5)₂CuLi H₂O+

3. Name this compound properly, including stereochemistry. H₂C H3C CH3 OH 4. Show the step(s) necessary to transform the compound on the left into the acid on the right. Bri CH2 5. Write in the product of this LiAlH4 Br H₂C OH

What are the major products of the following reaction? Please provide a detailed explanation and a drawing to show how the reaction proceeds.

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