The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn. Concept introduction: The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C 1 , instead the carbon to which it is attached is numbered as C 1 . As a substituent, the –COOH group is called as carboxyl group. To draw: The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

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Answer 1

Question

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

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Answer 2

Question

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

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Answer 3

Question

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

Expert Solution & Answer

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Answer 4

Question

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

Expert Solution & Answer

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Answer 5

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

Answer 6

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

Answer 7

Chapter 20.SE, Problem 34AP

Interpretation Introduction

Interpretation:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid is to be drawn.

Concept introduction:

The names of simple carboxylic acids which are derivatives of open-chain alkanes are arrived by replacing the terminal –e of the corresponding alkane name by –oic acid. The numbering starts from carboxyl carbon. Compounds with –COOH bonded to a ring are named using the suffix-carboxylic acid. The –COOH carbon in this case is not numbered as C₁, instead the carbon to which it is attached is numbered as C₁. As a substituent, the –COOH group is called as carboxyl group.

To draw:

The structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 20.1 - Give IUPAC names for the following compounds:Ch. 20.1 - Draw structures corresponding to the following...Ch. 20.2 - Prob. 3P Ch. 20.2 - The Ka for dichloroacetic acid is 3.32 Ă— 10-2....Ch. 20.3 - Calculate the percentages of dissociated and...Ch. 20.4 - Which would you expect to be a stronger acid, the...Ch. 20.4 - Dicarboxylic acids have two dissociation...Ch. 20.4 - The pKa of p-cyclopropylbenzoic acid is 4.45. Is...Ch. 20.4 - Prob. 9P Ch. 20.5 - Prob. 10P

Solution Summary: The author explains the structure of pregabalin with IUPAC name (S)-3-(aminomethyl) 5-methylhexanoic acid.

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