The systematic name and IUPAC name of each group substituent in the given molecules should be identified. Concept introduction: Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word. Prefix represents the substituent present in the molecule and its position in the root name. Suffix denotes the presence of functional group if any in the molecule. It can be an alkene , alkyne, alcohol, carboxylic acid , alcohol etc... For alkynes molecules, suffix will be ‘ yne ’. Root word represents the longest continuous carbon skeleton of the organic molecule. Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer . If the bulky groups are in opposite side then it is trans-isomer .

Question

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Answer 1

Question

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

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Answer 2

Question

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

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Answer 3

Question

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

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Answer 4

Question

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

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Answer 5

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

Answer 6

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

Answer 7

Chapter 9, Problem 32PP

(a)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

Answer 8

(a)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(a). 2,2,5-Trimethyl-3-hexene

Answer 9

(a)

Expert Solution

Answer 10

(a)

Expert Solution

Answer 11

Expert Solution

Answer 12

Explanation of Solution

The systematic name for the given molecule (a).

Draw the given molecule (a) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 1

(a). 2,2,5-Trimethyl-3-hexene

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 6 carbons. Hence the root name of the molecule is hexa. Since it is an alkyne with 6 carbons then hexane will be the parent carbon chain name.

The substituents present in the molecule are methyl, bromo (Br) groups on 2 and 5. Therefore on numbering the three methyl groups are present at 2 and 5. Positions is 2,2,5-Trimethyl.

Hence the systematic name for the molecule (a) is 2,2,5-Trimethyl-3-hexene

Answer 13

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

Answer 14

(b)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

Answer 15

(b)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(b). 4,4-Dichloro-2-hexene

Answer 16

(b)

Expert Solution

Answer 17

(b)

Expert Solution

Answer 18

Expert Solution

Answer 19

Explanation of Solution

The systematic name for the given structure (b).

Draw the given molecule (b) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 2

4,4-Dichloro-2-hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain six carbon atoms.

In the given molecule the parent carbon skeleton is linear in nature which consistes of 6 carbons so the root word for the molecule is 4,4- Dichloro-2-hexyne. The suffix ‘yne’ is used since it is an alkyne.

The substituent present in the molecule are 2-chloro atoms in C4 carbon.

Hence the systematic name for the molecule (b) is 4,4-Dichloro-2-hexyne.

Answer 20

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

Answer 21

(c)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

Answer 22

(c)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(c). 1-Hexyne

Answer 23

(c)

Expert Solution

Answer 24

(c)

Expert Solution

Answer 25

Expert Solution

Answer 26

Explanation of Solution

The systematic name for the given structure (c).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 3

1-Hexyne

The given molecule is drawn. The parent carbon skeleton is the longest continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is linear in nature which consists of 6 carbons so that root word for the molecule is 1-Hexyne. The suffix ‘yne’ is used since it is an alkyne.

The parent chain is numbered so that the triple bond is assigned the lowest possible locate (1 indicates that the the triple bond is located between C1 and C2).

Hence the systematic name for the molecule (c) is 1-Hexyne.

Answer 27

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.

Answer 28

(d)

Interpretation Introduction

Interpretation:

The systematic name and IUPAC name of each group substituent in the given molecules should be identified.

Concept introduction:

Any organic molecule can be named by using certain rules given by IUPAC (International Union for Pure and applied chemistry). IUPAC name consists of three parts in major namely Prefix suffix and root word.

Prefix represents the substituent present in the molecule and its position in the root name.

Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc...

For alkynes molecules, suffix will be ‘yne’.

Root word represents the longest continuous carbon skeleton of the organic molecule.

Two stereoisomers are there for an alkyne molecule. It depends upon the location of bulky group (or high molecular weight) on the triple bonded carbon atoms. If the bulky groups are in same side then it is cis-isomer. If the bulky groups are in opposite side then it is trans-isomer.

Answer 29

(d)

Expert Solution

Answer to Problem 32PP

Answer

The systematic names for the given molecules (a-c) are shown below.

(d). 3-Bromo-3-methyl-1-butyne

Answer 30

(d)

Expert Solution

Answer 31

(d)

Expert Solution

Answer 32

Expert Solution

Answer 33

Explanation of Solution

The systematic name for the given structure (d).

Draw the given molecule (d) and find the longest parent carbon chain or carbon skeleton and the substituents for naming the compound.

ORGANIC CHEMISTRY-NEXTGEN+BOX (2 SEM.), Chapter 9, Problem 32PP , additional homework tip 4

3-Bromo-3-methyl-1-butyne

The given molecule is drawn. The parent carbon skeleton is the continuous carbon chain that should contain more number of carbons. In the given molecule the parent carbon skeleton is the chain which contains 4 carbons. Hence the root name of the molecule is butane. Since it is an alkene with 4 carbons then butyne will be the parent carbon chain name.

In the given molecule parent chain is numbered so that the triple bond assigned the lowest possible locate (1 indicates that the triple bond is located between C₁ and C₂). The one methyl group, one bromo groups are present at C₃ positions is 3-Bromo-3-methyl (The alphabetized in the name, Br and CH₃).

Hence the systematic name for the molecule (a) is 3-Bromo-3-methyl-1-butyne.