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

+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

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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+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

→ Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?

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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