The structure of isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic 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 isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic acid.

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Answer 1

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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 20.SE, Problem 35AP

Interpretation Introduction

Interpretation:

The structure of isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic 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 isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic acid.

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The emission data in cps displayed in Table 1 is reported to two decimal places by the chemist. However, the instrument output is shown in Table 2. Table 2. Iron emission from ICP-AES Sample Blank Standard Emission, cps 579.503252562 9308340.13122 Unknown Sample 343.232365741 Did the chemist make the correct choice in how they choose to display the data up in Table 1? Choose the best explanation from the choices below. No. Since the instrument calculates 12 digits for all values, they should all be kept and not truncated. Doing so would eliminate significant information. No. Since the instrument calculates 5 decimal places for the standard, all of the values should be limited to the same number. The other decimal places are not significant for the blank and unknown sample. Yes. The way Saman made the standards was limited by the 250-mL volumetric flask. This glassware can report values to 2 decimal places, and this establishes our number of significant figures. Yes. Instrumental data…

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Answer 2

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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 20.SE, Problem 35AP

Interpretation Introduction

Interpretation:

The structure of isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic 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 isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic acid.

Expert Solution & Answer

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Check out a sample textbook solution

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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 20.SE, Problem 35AP

Interpretation Introduction

Interpretation:

The structure of isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic 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 isocitric acid which has the systematic name (2R, 3S)-3-carboxy-2-hydroxypentanedioic acid.

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 20.SE, Problem 35AP

Interpretation Introduction