(a) Interpretation: The IUPAC name of the given ester is to be provided. Concept introduction: IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the − oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Question

Want to see the full answer?

Answer 1

Question

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

> You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: 1. ☑ CI 2. H3O+ O Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. Explanation Check ? DO 18 Ar B © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility

Don't use ai to answer I will report you answer

Consider a solution of 0.00304 moles of 4-nitrobenzoic acid (pKa = 3.442) dissolved in 25 mL water and titrated with 0.0991 M NaOH. Calculate the pH at the equivalence point

Answer 2

Question

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 6

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 7

Chapter F, Problem F.22P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name of the given ester is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 8

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 9

Interpretation Introduction

(b)

Interpretation:

For the given ester, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 10

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 11

Interpretation Introduction

(c)

Interpretation:

For the given compound, the IUPAC name is to be provided.

Concept introduction:

IUPAC names of esters are made up of two parts, alkyl/aryl alkanoate, with the −oate suffix indicating that it is an ester. The alkanoate part is derived from the carboxylic acid from which the ester is formed. The longest carbon chain including the carbonyl carbon determines the root name of molecule. The alkyl/aryl part of the name of the alkyl or aryl group attached to the non-carbonyl oxygen of the ester group. Any lower priority functional groups are treated as substituents and named in the prefix of the corresponding part.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 15

Ch. F - Prob. F.1P Ch. F - Prob. F.2P Ch. F - Prob. F.3P Ch. F - Prob. F.4P Ch. F - Prob. F.5P Ch. F - Prob. F.6P Ch. F - Prob. F.7P Ch. F - Prob. F.8P Ch. F - Prob. F.9P Ch. F - Prob. F.10P

Solution Summary: The author explains that the IUPAC name of the given ester is propyl pentanoate.

Videos

Want to see the full answer?

Chapter F Solutions