ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
4th Edition
ISBN: 9781119838791
Author: Klein
Publisher: WILEY
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Chapter 22.11, Problem 27PTS

(a)

Interpretation Introduction

Interpretation: The given sets of azo dyes have to be prepared via an azo coupling reaction using the corresponding reactants which have to be identified.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  1

To find: Identify the reactants involved in the given product of azo dye via an azo coupling reaction (a)

Determine the ring which is more strongly activated

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  2

(b)

Interpretation Introduction

Interpretation: The given sets of azo dyes have to be prepared via an azo coupling reaction using the corresponding reactants which have to be identified.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  3

To find: Identify the reactants involved in the given product of azo dye via an azo coupling reaction (b)

Determine the ring which is more strongly activated

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  4

(c)

Interpretation Introduction

Interpretation: The given sets of azo dyes have to be prepared via an azo coupling reaction using the corresponding reactants which have to be identified.

Concept Introduction:

Aryldiazonium salts on coupling with an activated aromatic ring give an azo dye which produces a deep color in the final product.  This color is due to the extended conjugation in it.  This reaction occurs by electrophilic substitution reaction.  This method is called an azo coupling.  The obtained final compound is known as azo dyes.

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  5

To find: Identify the reactants involved in the given product of azo dye via an azo coupling reaction (c)

Determine the ring which is more strongly activated

ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<, Chapter 22.11, Problem 27PTS , additional homework tip  6

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Students have asked these similar questions
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

Chapter 22 Solutions

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