(a) Interpretation: Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted. Concept introduction: The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds. There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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Answer 1

Question

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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Can you please help mne with this problem. Im a visual person, so can you redraw it, potentislly color code and then as well explain it. I know im given CO2 use that to explain to me, as well as maybe give me a second example just to clarify even more with drawings (visuals) and explanations.

Part 1. Aqueous 0.010M AgNO 3 is slowly added to a 50-ml solution containing both carbonate [co32-] = 0.105 M and sulfate [soy] = 0.164 M anions. Given the ksp of Ag2CO3 and Ag₂ soy below. Answer the ff: Ag₂ CO3 = 2 Ag+ caq) + co} (aq) ksp = 8.10 × 10-12 Ag₂SO4 = 2Ag+(aq) + soy² (aq) ksp = 1.20 × 10-5 a) which salt will precipitate first? (b) What % of the first anion precipitated will remain in the solution. by the time the second anion starts to precipitate? (c) What is the effect of low pH (more acidic) condition on the separate of the carbonate and sulfate anions via silver precipitation? What is the effect of high pH (more basic)? Provide appropriate explanation per answer

Part 4. Butanoic acid (ka= 1.52× 10-5) has a partition coefficient of 3.0 (favors benzene) when distributed bet. water and benzene. What is the formal concentration of butanoic acid in each phase when 0.10M aqueous butanoic acid is extracted w❘ 25 mL of benzene 100 mL of a) at pit 5.00 b) at pH 9.00

Answer 2

Question

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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Answer 3

Question

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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Answer 4

Question

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

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Answer 5

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 6

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 7

Chapter 7, Problem 7.56AP

Interpretation Introduction

(a)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 8

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 9

Interpretation Introduction

(b)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 10

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 11

Interpretation Introduction

(c)

Interpretation:

Whether the given compound is conformational diastereomers, conformational enantiomers or identical is to be predicted.

Concept introduction:

The saturated six membered ring compounds are mostly expressed and explained in the chair conformations. This is because chair conformation is the most stable conformation of cyclohexane. Therefore, the chair conformation is most helpful in the studies of six carbon ring compounds.

There are two forms of chair conformation one is axial form if the substituent is at axial position and other is equatorial form if the substituent is at equatorial position.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 7 - Prob. 7.1P Ch. 7 - Prob. 7.2P Ch. 7 - Prob. 7.3P Ch. 7 - Prob. 7.4P Ch. 7 - Prob. 7.5P Ch. 7 - Prob. 7.6P Ch. 7 - Prob. 7.7P Ch. 7 - Prob. 7.8P Ch. 7 - Prob. 7.9P Ch. 7 - Prob. 7.10P

Solution Summary: The author explains that the saturated six-membered ring compounds are expressed and explained in the chair conformations.

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