a) Interpretation: How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown. Concept introduction: Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond. To show: How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Question

when performing the reaction that involves 2 equivalents of 3-(diethylamino)-phenol and Phthalic anhydride with sulfuric acid and water react to form rhodamine b where the Phthalic anhydride cleaves in acid and how does Excessive Washing (w/ Base) & Subsequent Resonance Structure get affected

Answer 1

Question

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

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when performing the reaction that involves 2 equivalents of 3-(diethylamino)-phenol and Phthalic anhydride with sulfuric acid and water react to form rhodamine b where the Phthalic anhydride cleaves in acid and how does Excessive Washing (w/ Base) & Subsequent Resonance Structure get affected

3. The strongest acid of the following compounds is ___.A. p-nitrophenol; B. m-nitrophenol; C. o-chlorophenol;D. p-methoxyphenol; E. o-methylphenol Please explain your steps and thought process. Thank you!

Using the general properties of equilibrium constants At a certain temperature, the equilibrium constant K for the following reaction is 1.3 × 10 4: Cl2(g) + CHCl3(g) HCl(g) + CC₁(g) Use this information to complete the following table. Suppose a 16. L reaction vessel is filled with 1.6 mol of HCI and 1.6 mol of CCl4. What can you say about the composition of the mixture in the vessel at equilibrium? There will be very little Cl2 and CHCl3. ☐ x10 There will be very little HCI and CCl4. Neither of the above is true. What is the equilibrium constant for the following reaction? Be sure your answer has the correct number of significant digits. HCl(g)+CC14(g) 12 Cl2(9)+CHCl3(9) K = 0 ☐ What is the equilibrium constant for the following reaction? Be sure your answer has the correct number of significant digits. 2 Cl₂(9)+2CHCl3(9) 2 HCl(9)+2CC₁₁(9) K = ✓ 00. 18 Ar

Answer 2

Question

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

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Answer 3

Question

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Expert Solution & Answer

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Answer 4

Question

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Expert Solution & Answer

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Answer 5

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 6

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 7

Chapter 9.SE, Problem 43AP

Interpretation Introduction

a)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 8

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 9

Interpretation Introduction

b)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts. Use of deuterium in the presence of Lindlar catalyst yields cis alkenes with the two deuterium atoms arranged on the same side of the double bond while reduction with Li in liquid deuterated ammonia yields trans alkenes with the two deuterium atoms arranged on the opposite sides of the double bond.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 10

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Answer 11

Interpretation Introduction

c)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺.

To show:

How to carry out the reaction given which yields deuterium incorporated alkyne as the product.

Answer 12

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 13

Interpretation Introduction

d)

Interpretation:

How to carry out the reaction given which yields deuterium incorporated alkene as the product is to be shown.

Concept introduction:

Deuterium incorporated alkynes can be prepared first by converting them in to alkynides by treating with NaNH₂ in NH₃ and then treating the alkynide obtained with D₃O⁺. The alkyne thus obtained when treated with deuterium in the presence of Lindlar catalyst yield an alkene with deuterium atom on both carbons.

To show:

How to carry out the reaction given which yields deuterium incorporated alkene as the product.

Answer 14

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Ch. 9.1 - Prob. 1P Ch. 9.1 - Prob. 2P Ch. 9.3 - What products would you expect from the following...Ch. 9.4 - Prob. 4P Ch. 9.4 - Prob. 5P Ch. 9.4 - Prob. 6P Ch. 9.4 - Prob. 7P Ch. 9.5 - Using any alkyne needed, how would you prepare the...Ch. 9.7 - The pKa of acetone, CH3COCH3, is 19.3. Which of...Ch. 9.8 - Prob. 10P

Solution Summary: The author explains how deuterium incorporated alkenes can be prepared from alkynes by reduction in the presence of catalysts.

Chapter 9 Solutions