(a) Interpretation: The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn. Concept introduction: For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

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Answer 1

Question

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

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Answer 2

Question

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

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Answer 3

Question

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

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Answer 4

Question

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

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Answer 5

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 6

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 7

Chapter B, Problem B.31P

Interpretation Introduction

(a)

Interpretation:

The structure for 2-methyl-1, 3, 5-hexatriene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The structure for 1, 6-dimethoxyhexa-1, 5-diene is to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicate the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 10

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 11

Interpretation Introduction

(b)

Interpretation:

The structures for penta-1, 4-diene and cyclopenta-1, 3-diene are to be drawn.

Concept introduction:

For a molecule that has more than one double bond, the IUPAC name indicates the number of double bonds present as well as their locations. To draw the structure from the given name, first, it is important to identify the root. The longest carbon chain or the largest carbon ring containing all the C=C groups is the root. The prefixes used in the IUPAC name such as di, tri indicates the number of double bonds in the root. The locator numbers added in the IUPAC name indicate the successive C=C groups as they are encountered in the root. Immediately before the ‘ene’ suffix, a letter ‘a’ is added followed by the above set of locator numbers. The substituents attached to the root are named in alphabetical order.

Answer 12

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Answer 13

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Answer 14

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Answer 15

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

Solution Summary: The structure for 2-methyl-1, 3, 5-hexatriene is drawn using the IUPAC name, which indicates the number of double bonds present and their locations.

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