(a) Interpretation: The enol form should be drawn for given compound. Concept Introduction: A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium. a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Question

Using the Nernst equation to calculate nonstandard cell voltage A galvanic cell at a temperature of 25.0 °C is powered by the following redox reaction: MnO2 (s)+4H* (aq)+2Cr²+ (aq) → Mn²+ (aq)+2H₂O (1)+2Cr³+ (aq) + 2+ 2+ 3+ Suppose the cell is prepared with 7.44 M H* and 0.485 M Cr²+ in one half-cell and 7.92 M Mn² and 3.73 M Cr³+ in the other. Calculate the cell voltage under these conditions. Round your answer to 3 significant digits. ☐ x10 μ Х 5 ? 000 日。

Answer 1

Question

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

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Using the Nernst equation to calculate nonstandard cell voltage A galvanic cell at a temperature of 25.0 °C is powered by the following redox reaction: MnO2 (s)+4H* (aq)+2Cr²+ (aq) → Mn²+ (aq)+2H₂O (1)+2Cr³+ (aq) + 2+ 2+ 3+ Suppose the cell is prepared with 7.44 M H* and 0.485 M Cr²+ in one half-cell and 7.92 M Mn² and 3.73 M Cr³+ in the other. Calculate the cell voltage under these conditions. Round your answer to 3 significant digits. ☐ x10 μ Х 5 ? 000 日。

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Calculating the pH of a weak base titrated with a strong acid b An analytical chemist is titrating 116.9 mL of a 0.7700M solution of aniline (C6H5NH2) with a 0.5300M solution of HNO3. The pK of aniline is 9.37. Calculate the pH of the base solution after the chemist has added 184.2 mL of the HNO 3 solution to it. Note for advanced students: you may assume the final volume equals the initial volume of the solution plus the volume of HNO3 solution added. Round your answer to 2 decimal places. pH = ☐ ☑ 5

Answer 2

Question

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

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Answer 3

Question

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

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Answer 4

Question

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

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Answer 5

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Answer 6

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Answer 7

Chapter 16, Problem 36P

Interpretation Introduction

(a)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a- hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The enol form should be drawn for given compound.

Concept Introduction:

A carbonyl compound that has a -hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound doesn’t have any a -hydrogen is does not undergo Keto-Enol tautomerism.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The enol form should be drawn for given compound.

.

Concept Introduction:

A carbonyl compound that has a hydrogen on a a-carbon changes its form to enol through resonance. Both the form stays in equilibrium.

a hydrogen is the hydrogen which attached to a a-carbon for a carbonyl compound. a-carbon is carbon adjacent to the carbonyl carbon. If a compound don’t have any a hydrogen is does not undergo Keto-Enol tautomerism.

Answer 12

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Ch. 16.2 - Problem 17-1 Wrtie the IUPAC name for each...Ch. 16.2 - Prob. 16.2QC Ch. 16.2 - Prob. 16.3QC Ch. 16.4 - Prob. 16.4QC Ch. 16.4 - Prob. 16.5QC Ch. 16.4 - Problem 17-6 Show the reaction of benzaldehyde...Ch. 16.4 - Problem 17-7 Identify all hemiacetals and acetals...Ch. 16.5 - Prob. 16.8QC Ch. 16 - 17-9 Answer true or false. (a) The one aldehyde...Ch. 16 - Prob. 2P

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