(a) Interpretation: The IUPAC name for the given compound is to be assigned. Concept introduction: In naming organic compounds, the functional groups , other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Question

Want to see the full answer?

Answer 1

Question

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

What is the molar mass of a gas that takes three times longer to effuse than helium?

First image: I have to show the mecanism (with arows and structures) of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary Second image: I have to show the mecanism (with arrows and structures) for the reaction on the left, where the alcohol A is added fast in one portion its not an exam

what is the skeletal structure of a tertiary alkyl fluoride with six carbon atoms and no rings.

Answer 2

Question

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Answer 6

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Answer 7

Chapter E, Problem E.45P

Interpretation Introduction

(a)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups, other than highest priority functional groups, are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. Number the carbon chain in a way the functional group and the substituents attached to it gets the lowest number. The position of the functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing the functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ ending and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from‘ane’, ‘ene’, or ‘yne’ from the ending, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get the lowest number. The position of functional group and substituents on the parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in an alphabetical order when writing the IUPAC name.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The IUPAC name for the given compound is to be assigned.

Concept introduction:

In naming organic compounds, the functional groups other than highest priority functional groups are treated as substituents. The root name is established by identifying the longest carbon chain or a ring containing functional group. Remove the “e” from the normal ‘ane’, ‘ene’, or ‘yne’ and add the suffix that corresponds to the highest-priority functional group. If the highest priority group is present twice, there is no need to remove ‘e’ from ‘ane’, ‘ene’, or ‘yne’, and prefixes are used to denote the number of identical functional groups. Number the carbon chain in a way that the functional group and the substituents attached get lowest number. The position of functional group and substituents on parent chain or ring is indicated by the respective locant number just before the suffix. The substituents are written in alphabetical order when writing the IUPAC name. The stereochemistry of bond is indicated by E/Z notation. E represents the trans double bond where the same priority groups are on opposite side of double bond. Z represents the cis double bond where the same priority groups are on same side of the double bond.

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

Solution Summary: The author explains the IUPAC name for the given compound by identifying the longest carbon chain or a ring containing functional group.

Concept explainers

Videos

Want to see the full answer?

Chapter E Solutions