The nature and behaviour of vinylidene chloride needs to be explained in this problem, due to which it does not shows any of the three stereochemical outcomes. Concept introduction: Isotactic, syndiotactic, and atactic are the stereochemical forms. The polymer having the (-R) group on the same side of the macromolecule backbone (zigzag bone) is known as isotactic polymer. An isotactic macromolecule consists of 100% meso diads. Syndiotactic are the macromolecules in which the (-R) groups are arranged in an alternate manner along the long chain of the polymer. Gutta percha is also an example for Syndiotactic polymer. In atactic form the substituents are placed in a random manner along the long chain. The important point to note here is that the polymer obtained from the chain growth polymerization mechanism must have chiral carbons to possess these structures. If the polymer formed does not have chiral carbon then it cannot occur in isotactic, syndiotactic and atactic forms.

Question

Use the vapor-liquid equilibrium data at 1.0 atm. for methanol-water (Table 2-8 ) for the following: If the methanol vapor mole fraction is 0.600, what is the methanol liquid mole fraction? Is there an azeotrope in the methanol-water system at a pressure of 1.0 atmospheres? If water liquid mole fraction is 0.350, what is the water vapor mole fraction? What are the K values of methanol and of water at a methanol mole fraction in the liquid of 0.200? What is the relative volatility αM-W at a methanol mole fraction in the liquid of 0.200?

Answer 1

Question

Definition Definition Chemical process in which one or more monomers combine to produce a very large chain-like molecule called a polymer. The functional groups present on the monomers and their steric effects are responsible for polymerization through a sequence of reactions that vary in complexity. There exists a stable covalent chemical bond between monomers that sets apart polymerization from other processes.

Chapter 31.2, Problem 4P

Interpretation Introduction

Interpretation:

The nature and behaviour of vinylidene chloride needs to be explained in this problem, due to which it does not shows any of the three stereochemical outcomes.

Concept introduction:

Isotactic, syndiotactic, and atactic are the stereochemical forms. The polymer having the (-R) group on the same side of the macromolecule backbone (zigzag bone) is known as isotactic polymer. An isotactic macromolecule consists of 100% meso diads.

Syndiotactic are the macromolecules in which the (-R) groups are arranged in an alternate manner along the long chain of the polymer. Gutta percha is also an example for Syndiotactic polymer.

In atactic form the substituents are placed in a random manner along the long chain.

The important point to note here is that the polymer obtained from the chain growth polymerization mechanism must have chiral carbons to possess these structures. If the polymer formed does not have chiral carbon then it cannot occur in isotactic, syndiotactic and atactic forms.

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Use the vapor-liquid equilibrium data at 1.0 atm. for methanol-water (Table 2-8 ) for the following: If the methanol vapor mole fraction is 0.600, what is the methanol liquid mole fraction? Is there an azeotrope in the methanol-water system at a pressure of 1.0 atmospheres? If water liquid mole fraction is 0.350, what is the water vapor mole fraction? What are the K values of methanol and of water at a methanol mole fraction in the liquid of 0.200? What is the relative volatility αM-W at a methanol mole fraction in the liquid of 0.200?

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Answer 2

Question

Definition Definition Chemical process in which one or more monomers combine to produce a very large chain-like molecule called a polymer. The functional groups present on the monomers and their steric effects are responsible for polymerization through a sequence of reactions that vary in complexity. There exists a stable covalent chemical bond between monomers that sets apart polymerization from other processes.

Chapter 31.2, Problem 4P

Interpretation Introduction

Interpretation:

The nature and behaviour of vinylidene chloride needs to be explained in this problem, due to which it does not shows any of the three stereochemical outcomes.

Concept introduction:

Isotactic, syndiotactic, and atactic are the stereochemical forms. The polymer having the (-R) group on the same side of the macromolecule backbone (zigzag bone) is known as isotactic polymer. An isotactic macromolecule consists of 100% meso diads.

Syndiotactic are the macromolecules in which the (-R) groups are arranged in an alternate manner along the long chain of the polymer. Gutta percha is also an example for Syndiotactic polymer.

In atactic form the substituents are placed in a random manner along the long chain.

The important point to note here is that the polymer obtained from the chain growth polymerization mechanism must have chiral carbons to possess these structures. If the polymer formed does not have chiral carbon then it cannot occur in isotactic, syndiotactic and atactic forms.

Expert Solution & Answer

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Check out sample textbook solution

Answer 3

Question

Definition Definition Chemical process in which one or more monomers combine to produce a very large chain-like molecule called a polymer. The functional groups present on the monomers and their steric effects are responsible for polymerization through a sequence of reactions that vary in complexity. There exists a stable covalent chemical bond between monomers that sets apart polymerization from other processes.

Chapter 31.2, Problem 4P

Interpretation Introduction

Interpretation:

The nature and behaviour of vinylidene chloride needs to be explained in this problem, due to which it does not shows any of the three stereochemical outcomes.

Concept introduction:

Isotactic, syndiotactic, and atactic are the stereochemical forms. The polymer having the (-R) group on the same side of the macromolecule backbone (zigzag bone) is known as isotactic polymer. An isotactic macromolecule consists of 100% meso diads.

Syndiotactic are the macromolecules in which the (-R) groups are arranged in an alternate manner along the long chain of the polymer. Gutta percha is also an example for Syndiotactic polymer.

In atactic form the substituents are placed in a random manner along the long chain.

The important point to note here is that the polymer obtained from the chain growth polymerization mechanism must have chiral carbons to possess these structures. If the polymer formed does not have chiral carbon then it cannot occur in isotactic, syndiotactic and atactic forms.

Expert Solution & Answer

Trending nowThis is a popular solution!

See solution

Check out sample textbook solution

Answer 4

Question

Definition Definition Chemical process in which one or more monomers combine to produce a very large chain-like molecule called a polymer. The functional groups present on the monomers and their steric effects are responsible for polymerization through a sequence of reactions that vary in complexity. There exists a stable covalent chemical bond between monomers that sets apart polymerization from other processes.

Chapter 31.2, Problem 4P

Interpretation Introduction