IUPAC name of the given compound has to be assigned. Concept Introduction: IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine. Longest carbon chain has to be identified that is attached to nitrogen atom. Suffix “-e” in name of the parent chain alkane is replaced by “-amine”. Numbering of the carbon chain is done from the end that is near the nitrogen atom. Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name. In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name. If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N -substituted primary amines. Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine. In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

Question

Want to see the full answer?

Answer 1

Question

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Explain why the following names of the structures are incorrect. CH2CH3 CH3-C=CH-CH2-CH3 a. 2-ethyl-2-pentene CH3 | CH3-CH-CH2-CH=CH2 b. 2-methyl-4-pentene

Draw the line-angle formula of cis-2,3-dichloro-2-pentene. Then, draw the line-angle formula of trans-2,3-dichloro-2-pentene below. Draw the dash-wedge formula of cis-1,3-dimethylcyclohexane. Then, draw the dash-wedge formula of trans-1,3-dimethylcyclohexane below.

Record the amounts measured and calculate the percent yield for Part 2 in the table below. Dicyclopentadiene measured in volume Cyclopentadiene measured in grams 0 Measured Calculated Mol Yield Mass (g) or Volume (mL) Mass (g) or Volume (ml) 0.6 2.955 Part 2 Measurements and Results Record the amounts measured and calculate the percent yield for Part 2 in the table below. 0.588 0.0044 2.868 0.0434 N/A Table view List view Measured Calculated Mol $ Yield Melting Point (C) Mass (g) or Volume (ml) Mass (g) or Volume (ml.) Cyclopentadiene 0.1 0.08 0.001189 measured in volume Maleic Anhydride 0.196 N/A cis-norbornene-5,6-endo- dicarboxylic anhydride 0.041 0.0002467 N/A N/A N/A 0.002 N/A N/A 128

Answer 2

Question

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Answer 6

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

Answer 7

Chapter 17, Problem 17.116EP

(a)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

Answer 8

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Answer 9

(b)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Answer 10

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

Answer 11

(c)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

IUPAC nomenclature for amine: There are about five rules to be followed in giving IUPAC name for an amine.

Longest carbon chain has to be identified that is attached to nitrogen atom.

Suffix “-e” in name of the parent chain alkane is replaced by “-amine”.

Numbering of the carbon chain is done from the end that is near the nitrogen atom.

Point of attachment of the nitrogen atom in the carbon chain is indicated by a number before the parent chain name.

In case if substituents are present, then the identity and location of substituents are appended to the front in the parent chain name.

If the compound contains two amine groups, then the suffix “-e” is replaced by diamine. Tertiary and secondary amines are named as N-substituted primary amines.

Common name for amine is given in a single word. Primary amine is named as alkylamine. Secondary amine is named as alkylalkylamine. Tertiary amine is named as alkylalkylalkylamine.

In a line-angle structural formula, the point of intersection and the end points represent a carbon atom.

Answer 12

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Answer 13

(d)

Interpretation Introduction

Interpretation:

IUPAC name of the given compound has to be assigned.

Concept Introduction:

Amides are derivatives of carboxylic acid. This is the reason that their names are completely based on the parent carboxylic acid.

IUPAC rules for naming an amide:

The end in name of the carboxylic acid is changed from “-ic acid” or “-oic acid” to “-amide”.

The groups attached to the nitrogen are appended to front of base name by using N-prefix as locator.

For amides, IUPAC name and common names are given using the same rules.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 17.1 - Prob. 1QQ Ch. 17.1 - Prob. 2QQ Ch. 17.2 - Prob. 1QQ Ch. 17.2 - Prob. 2QQ Ch. 17.2 - Prob. 3QQ Ch. 17.2 - Prob. 4QQ Ch. 17.3 - Prob. 1QQ Ch. 17.3 - Prob. 2QQ Ch. 17.3 - Prob. 3QQ Ch. 17.3 - Prob. 4QQ

Solution Summary: The author explains the IUPAC nomenclature for an amine. The longest carbon chain attached to the nitrogen atom is identified.

Concept explainers

Want to see the full answer?

Chapter 17 Solutions