The expected product has to be drawn for the given reaction. Concept Introduction: Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is s p hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond. Ozonolysis of Alkynes: Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne, If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid . The general scheme can be shown for the reaction that involves terminal alkyne is,

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Answer 1

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

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Name 1) 3-fluoro, 1-butene 2) 2-heptene 2,3-difluoro- 1-pentene 4) 6-iodo,4-methyl- 2-decyne 5) 4,4-dibromo- 1,2-butandiol Complete structural formula F -C=C-C-C- Line formula Condensed structural formula N F CH2=CHCHFCH3

1. Part 1: Naming Organic Compounds он H₁C-C-CH3 CH3 Br CI CI 2. Br-CH-CH-CH₂ H₂C-CH-C= -CH-CH2-CH3 3. HC-CH-CH-C-OH 5. H₂C-CH-CH₂-OH 7. OH 4. CH CH₂-CH₂ 6. сно CH-CH-CH-CH₂-CH₂ H₁₂C-CH-CH-CH-CH₁₂-CH₁₂ 8. OH

11 Organic Chemistry Organic Nomenclature Practice Name/Functional Group n-butane Formula Structural Formula (1) C4tt10 H3C C- (2) CH3CH2CH2 CH 3 H₂ -CH3 Н2 name & functional group (1) and (2) OH H₁₂C Н2 name only (1) and (2) name only (1) and (2) H₁C - = - CH₂ Н2 HC=C-C CH3

Answer 2

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

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Answer 3

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 4

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

Want to see more full solutions like this?

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Answer 5

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

Answer 6

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6

Conclusion

The expected product was drawn for the given reaction.

Answer 7

Chapter 12.7, Problem 12.35P

Interpretation Introduction

Interpretation:

The expected product has to be drawn for the given reaction.

Concept Introduction:

Alkynes are the compounds that contain a triple bond between two carbon atoms. The carbon atom present in the triple bond is sp hybridised. Due to this, the geometry of alkyne will be linear. Terminal alkyne are the one which has a proton attached to the triple bond and internal alkyne are the one in which there are no protons attached to the triple bond.

Ozonolysis of Alkynes:

Alkynes undergo ozonolysis with ozone. The reaction that takes place when an alkyne is treated with ozone is that an oxidative cleavage. This is followed by treatment with water to give carboxylic acids as products. If the considered alkyne is an internal alkyne then the product will be two carboxylic acids. The general scheme can be shown as given below for reaction involving internal alkyne,

If the alkyne that is considered is a terminal alkyne, then the terminal end is converted into carbon dioxide and the other end gets converted to carboxylic acid. The general scheme can be shown for the reaction that involves terminal alkyne is,

Answer 8

Expert Solution & Answer

Answer to Problem 12.35P

The expected product is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 4

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Explanation of Solution

Given reaction is,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 5

From the given reaction condition, it is clear that the given reaction is ozonolysis reaction. The considered alkyne is an internal alkyne. Hence, two carboxylic acids will be obtained as products from oxidative cleavage of alkyne. This can be shown as given below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 12.7, Problem 12.35P , additional homework tip 6