(a) Interpretation: How to synthesize the given compound from an alkyne is to be described. Concept introduction: The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

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Answer 1

Question

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

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You are a Quality Manager for a very well-known food ingredient company that produces umami powder, and you are responsible for setting specification limits. The net weight (in grams) of bags of unami powder is monitored by taking samples of six bags on an hourly basis during production. The label on every bag reports a contents of 1KG umami powder. The process mean is μ = 1012 g, and when the process is properly adjusted, it varies with σ = 11 g. QUESTION: Provide a valid and full justification as to whether you would advise your manager that the process is satisfactory when it is properly adjusted, or would you seek their approval to improve the process?

You are a Quality Manager for a very well-known food ingredient company that produces umami powder, and you are responsible for setting specification limits. The net weight (in grams) of bags of unami powder is monitored by taking samples of six bags on an hourly basis during production. The label on every bag reports a contents of 1KG umami powder. The process mean is μ = 1012 g, and when the process is properly adjusted, it varies with σ = 11 g. QUESTION: Using all the available information, set the upper and lower specification limits.

43) 10.00 ml of vinegar (active ingredient is acetic acid) is titrated to the endpoint using 19.32 ml of 0.250 M sodium hydroxide. What is the molarity of acetic acid in the vinegar? YOU MUST SHOW YOUR WORK. NOTE: MA x VA = MB x VB

Answer 2

Question

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

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Answer 3

Question

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

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Answer 4

Question

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

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Answer 5

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

Answer 6

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Answer 7

Chapter 11, Problem 11.14P

Interpretation Introduction

(a)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen chloride is used as a reagent, the reaction goes through vinylic carbocation intermediate as the chlorine atom will stabilize the positive charge on the carbon atom through resonance. The alkyne must be symmetric to avoid producing a mixture of isomers.

Answer 8

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

Answer 9

Interpretation Introduction

(b)

Interpretation:

How to synthesize the given compound from an alkyne is to be described.

Concept introduction:

The carbon-carbon triple bond in terminal alkynes is electron rich and thus undergoes electrophilic addition reaction with a strong Bronsted acid such as hydrogen halide. Addition of two equivalents of hydrogen halide to a terminal alkyne produces a geminal dihalide, in which both the halide atoms are on the same carbon atom. The regioselectivity is in accordance with the Markovnikov’s rule. The hydrogen halide adds twice to generate the geminal dihalide. If hydrogen bromide is used as a reagent, the reaction goes through formation of a pi complex with an alkyne. This pi complex is stabilized by the attraction between electron rich triple bond and electron poor proton of the acid. The alkyne must be symmetric to avoid producing a mixture of isomers. An unsymmetric alkyne produces a mixture of isomers.

Answer 10

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Answer 13

Ch. 11 - Prob. 11.1P Ch. 11 - Prob. 11.2P Ch. 11 - Prob. 11.3P Ch. 11 - Prob. 11.4P Ch. 11 - Prob. 11.5P Ch. 11 - Prob. 11.6P Ch. 11 - Prob. 11.7P Ch. 11 - Prob. 11.8P Ch. 11 - Prob. 11.9P Ch. 11 - Prob. 11.10P

Solution Summary: The author explains how to synthesize the given compound from an alkyne.

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