The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined. Concept introduction: 舧 Amino acids are organic compounds containing amine ( − NH 2 ) and carboxyl ( − COOH ) functional group along with a side chain (R group) specific to each amino acid. 舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid. The general reaction is as: 舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α − amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine. 舧 Acrolein and methanethiol on treating with a base gives 3 − ( methylthio ) propanal , which when subjected to Strecker synthesis forms imine from 3 − ( methylthio ) propanal and ammonia, which on addition of hydrogen cyanide produces α − amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

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Answer 1

Question

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

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Answer 2

Question

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

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Answer 3

Question

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

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Answer 4

Question

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

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Answer 5

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

Answer 6

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

Answer 7

Chapter 24, Problem 4PP

Interpretation Introduction

Interpretation:

The Strecker synthesis of DL-phenylalanine is to be outlined, and by preparing the starting aldehyde using acrolein and methanethiol, Strecker synthesis of DL-methanethiol is to be outlined.

Concept introduction:

舧 Amino acids are organic compounds containing amine (−NH2) and carboxyl (−COOH) functional group along with a side chain (R group) specific to each amino acid.

舧 Strecker synthesis involves treating an aldehyde with ammonia and hydrogen cyanide to give an aminonitrile, which can be hydrolyzed to an αa-amino acid.

The general reaction is as:

舧 The Strecker synthesis involves formation of imine from phenyl acetaldehyde and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis to yield DL-phenylalanine.

舧 Acrolein and methanethiol on treating with a base gives 3−(methylthio)propanal, which when subjected to Strecker synthesis forms imine from 3−(methylthio)propanal and ammonia, which on addition of hydrogen cyanide produces α− amino nitrile, and further undergoes hydrolysis in the second step to yield DL-Methionine.

Answer 8

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Answer 11

Ch. 24 - Prob. 1PP Ch. 24 - Practice Problem 24.2 The guanidino group NHNHCNH2...Ch. 24 - Prob. 3PP Ch. 24 - Prob. 4PP Ch. 24 - Prob. 5PP Ch. 24 - Prob. 6PP Ch. 24 - Prob. 7PP Ch. 24 - Practice Problem 24.8 Glutathione is a tripeptide...Ch. 24 - Prob. 9PP Ch. 24 - Prob. 10PP

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