(a) Interpretation: The IUPAC name for the given compound is to be written. Concept introduction: The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups , the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name. If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

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Answer 1

Question

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

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For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? NH2 MgBr Will the first product that forms in this reaction create a new CC bond? ○ Yes ○ No MgBr ? Will the first product that forms in this reaction create a new CC bond? O Yes O No Click and drag to start drawing a structure. :☐ G x c olo Ar HE

Predicting As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C - C bond as its major product: H₂N O H 1. ? 2. H3O+ If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. 0 If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. فا Explanation Check Click and drag to start drawing a structure.

Highlight the chirality (or stereogenic) center(s) in the given compound. A compound may have one or more stereogenic centers. OH OH OH OH OH OH

Answer 2

Question

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

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Answer 3

Question

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

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Answer 4

Question

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

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Answer 5

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 6

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 7

Chapter F, Problem F.2P

Interpretation Introduction

(a)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of the ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 8

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 9

Interpretation Introduction

(b)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 10

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 11

Interpretation Introduction

(c)

Interpretation:

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

Concept introduction:

The IUPAC name of a compound is made of three parts, prefix, root, and suffix. If the compound contains different functional groups, the highest priority group is determined. This determines the suffix. The longest continuous chain of carbons that contains the highest priority group forms the root. The final ‘e’ in the name of the corresponding alkane is replaced by the suffix corresponding to the highest priority group, except in case of nitriles, when the suffix ‘nitrile’ is simply added to the root name. The position (locant) of the highest priority group on the longest chain is inserted between the root name and the suffix unless redundant. The longest carbon chain is numbered in the direction that gives the highest priority group the lowest possible locant. If the root is a ring, the position of highest priority group is always 1. Any other low priority groups are treated as substituents and listed alphabetically in the prefix along with their locants. In case of rings, the numbering of ring carbons is done in the direction that gives the substituents the lowest possible locants. If more than one instance of any functional group (including highest priority) is present, their numbers are specified by adding a di, tri, etc. to the respective functional group name.

If any chiral carbons are present, their absolute configurations are determined on the basis of Cahn-Ingold-Prelog rules, and listed at the start along with the carbon number.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

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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 a compound is made of three parts, prefix, root, and suffix.

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