General, Organic, & Biological Chemistry
General, Organic, & Biological Chemistry
3rd Edition
ISBN: 9780073511245
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Chapter 17, Problem 17.43P
Interpretation Introduction

(a)

Interpretation:

The acceptable name for the following carboxylic acid should be determined:

  General, Organic, & Biological Chemistry, Chapter 17, Problem 17.43P , additional homework tip  1

Concept introduction:

An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.

In order to give the name to the carboxylic acid group, the following steps are followed:

1. The parent (longest) alkane chain is identified.

2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.

3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.

4. Name should be written in alphabetical order and other substituents are shown by the number.

For number of carbons atoms chain, the prefix is given as:

Carbon-1  meth

Carbon-2  eth

Carbon-3  prop

Carbon-4  but

Carbon-5  pent

Carbon-6  hex

Carbon-7  hept

Carbon-8  oct

Carbon-9  non

Carbon-10  dec

Interpretation Introduction

(b)

Interpretation:

The acceptable name for the following carboxylic acid should be determined:

  General, Organic, & Biological Chemistry, Chapter 17, Problem 17.43P , additional homework tip  2

Concept introduction:

An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.

In order to give the name to the carboxylic acid group, the following steps are followed:

1. The parent (longest) alkane chain is identified.

2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.

3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.

4. Name should be written in alphabetical order and other substituents are shown by the number.

For number of carbons atoms chain, the prefix is given as:

Carbon-1  meth

Carbon-2  eth

Carbon-3  prop

Carbon-4  but

Carbon-5  pent

Carbon-6  hex

Carbon-7  hept

Carbon-8  oct

Carbon-9  non

Carbon-10  dec

Interpretation Introduction

(c)

Interpretation:

The acceptable name for the following carboxylic acid should be determined:

  General, Organic, & Biological Chemistry, Chapter 17, Problem 17.43P , additional homework tip  3

Concept introduction:

An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.

In order to give the name to the carboxylic acid group, the following steps are followed:

1. The parent (longest) alkane chain is identified.

2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.

3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.

4. Name should be written in alphabetical order and other substituents are shown by the number.

For number of carbons atoms chain, the prefix is given as:

Carbon-1  meth

Carbon-2  eth

Carbon-3  prop

Carbon-4  but

Carbon-5  pent

Carbon-6  hex

Carbon-7  hept

Carbon-8  oct

Carbon-9  non

Carbon-10  dec

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Chapter 17 Solutions

General, Organic, & Biological Chemistry

Ch. 17.2 - Prob. 17.11PCh. 17.3 - Which compound in each pair has the higher boiling...Ch. 17.4 - Prob. 17.13PCh. 17.5 - In addition to ethyl butanoate (Section 17.5),...Ch. 17.6 - Prob. 17.15PCh. 17.6 - Prob. 17.16PCh. 17.6 - Prob. 17.17PCh. 17.6 - Prob. 17.18PCh. 17.6 - Prob. 17.19PCh. 17.7 - Prob. 17.20PCh. 17.7 - Ibuprofen is another pain reliever that is a...Ch. 17.8 - Prob. 17.22PCh. 17.8 - Prob. 17.23PCh. 17.8 - Prob. 17.24PCh. 17.8 - Prob. 17.25PCh. 17.8 - Prob. 17.26PCh. 17.9 - Prob. 17.27PCh. 17.9 - Prob. 17.28PCh. 17.9 - Prob. 17.29PCh. 17.9 - Prob. 17.30PCh. 17.9 - Prob. 17.31PCh. 17.9 - Prob. 17.32PCh. 17.10 - Prob. 17.33PCh. 17.10 - Prob. 17.34PCh. 17.10 - Prob. 17.35PCh. 17.11 - Prob. 17.36PCh. 17 - Prob. 17.37PCh. 17 - Prob. 17.38PCh. 17 - Prob. 17.39PCh. 17 - Prob. 17.40PCh. 17 - Prob. 17.41PCh. 17 - Prob. 17.42PCh. 17 - Prob. 17.43PCh. 17 - Prob. 17.44PCh. 17 - Prob. 17.45PCh. 17 - Prob. 17.46PCh. 17 - Prob. 17.47PCh. 17 - Give an acceptable name for each ester. a. CH3CO2(...Ch. 17 - Prob. 17.49PCh. 17 - Prob. 17.50PCh. 17 - Prob. 17.51PCh. 17 - Give an acceptable name for each compound. a. b....Ch. 17 - Prob. 17.53PCh. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Prob. 17.57PCh. 17 - Prob. 17.58PCh. 17 - Prob. 17.59PCh. 17 - Prob. 17.60PCh. 17 - Prob. 17.61PCh. 17 - Prob. 17.62PCh. 17 - Prob. 17.63PCh. 17 - Prob. 17.64PCh. 17 - Prob. 17.65PCh. 17 - Prob. 17.66PCh. 17 - What ester is formed when butanoic acid...Ch. 17 - Prob. 17.68PCh. 17 - Prob. 17.69PCh. 17 - Prob. 17.70PCh. 17 - Prob. 17.71PCh. 17 - Prob. 17.72PCh. 17 - Prob. 17.73PCh. 17 - Prob. 17.74PCh. 17 - Prob. 17.75PCh. 17 - Prob. 17.76PCh. 17 - Prob. 17.77PCh. 17 - Prob. 17.78PCh. 17 - Prob. 17.79PCh. 17 - Prob. 17.80PCh. 17 - Prob. 17.81PCh. 17 - Prob. 17.82PCh. 17 - Prob. 17.83PCh. 17 - Prob. 17.84PCh. 17 - Prob. 17.85PCh. 17 - Prob. 17.86PCh. 17 - What is the difference between saponification and...Ch. 17 - You have now learned three different types of...Ch. 17 - Draw the products formed in each reaction. Ch. 17 - Prob. 17.90PCh. 17 - Answer the following questions about A, depicted...Ch. 17 - Answer the following questions about B, depicted...Ch. 17 - Prob. 17.93PCh. 17 - Prob. 17.94PCh. 17 - Prob. 17.95PCh. 17 - Prob. 17.96PCh. 17 - Prob. 17.97PCh. 17 - Prob. 17.98PCh. 17 - Prob. 17.99PCh. 17 - Prob. 17.100PCh. 17 - Prob. 17.101PCh. 17 - Prob. 17.102PCh. 17 - Prob. 17.103CPCh. 17 - Lactams can be hydrolyzed with base, just like...
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