ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<
ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<
2nd Edition
ISBN: 9781118872925
Author: Klein
Publisher: JOHN WILEY+SONS INC.CUSTOM
Question
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Chapter 17.11, Problem 29PTS

(a)

Interpretation Introduction

Interpretation:

The expected value for λmax of the given compounds should be determined by using Woodward-Fieser rule.

Concept introduction:

  • The π-systems of conjugated dienes absorb UV or visible light (200nm – 800nm).
  • The wavelength of maximum absorption of a compound is called λmax .
  • The value of λmax is highly depending on the extent of conjugation (number of conjugated double bonds).                                                                                                       Conjugated double bonds are the C=C bonds, which are separated by one σ-bond.
  • According to Woodward-Fieser rule, the portion of the molecule which absorbs UV-visible light is called chromophore and the groups attached to the chromophore are auxochromes. Woodward-Fieser rule gives the estimate value for λmax .
  • The estimate value for λmax are given in below table,
FEATURES λmax - value Example Calculation
Conjugated- diene

  Base value

    = 217

  ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  1    217 nm
Each additional double bond

     +30

ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  2

Base: 217

+2×30

Each auxochromic alkyl group

      +5

           ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  3

 Base: 217                   +3×5

Each exocyclic double bond

      +5

                      ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  4

Base: 217

     + 5

Homoannular diene (both double bonds are situated in a ring)

    + 39

            ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  5

Base: 217

    +39

(b)

Interpretation Introduction

Interpretation:

The expected value for λmax of the given compounds should be determined by using Woodward-Fieser rule.

Concept introduction:

  • The π-systems of conjugated dienes absorb UV or visible light (200nm – 800nm).
  • The wavelength of maximum absorption of a compound is called λmax .
  • The value of λmax is highly depending on the extent of conjugation (number of conjugated double bonds).                                                                                                       Conjugated double bonds are the C=C bonds, which are separated by one σ-bond.
  • According to Woodward-Fieser rule, the portion of the molecule which absorbs UV-visible light is called chromophore and the groups attached to the chromophore are auxochromes. Woodward-Fieser rule gives the estimate value for λmax .
  • The estimate value for λmax are given in below table,
FEATURES λmax - value Example Calculation
Conjugated- diene

  Base value

    = 217

  ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  6    217 nm
Each additional double bond

     +30

ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  7

Base: 217

+2×30

Each auxochromic alkyl group

      +5

           ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  8

 Base: 217                   +3×5

Each exocyclic double bond

      +5

                      ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  9

Base: 217

     + 5

Homoannular diene (both double bonds are situated in a ring)

    + 39

            ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  10

Base: 217

    +39

(c)

Interpretation Introduction

Interpretation:

The expected value for λmax of the given compounds should be determined by using Woodward-Fieser rule.

Concept introduction:

  • The π-systems of conjugated dienes absorb UV or visible light (200nm – 800nm).
  • The wavelength of maximum absorption of a compound is called λmax .
  • The value of λmax is highly depending on the extent of conjugation (number of conjugated double bonds).                                                                                                       Conjugated double bonds are the C=C bonds, which are separated by one σ-bond.
  • According to Woodward-Fieser rule, the portion of the molecule which absorbs UV-visible light is called chromophore and the groups attached to the chromophore are auxochromes. Woodward-Fieser rule gives the estimate value for λmax .
  • The estimate value for λmax are given in below table,
FEATURES λmax - value Example Calculation
Conjugated- diene

  Base value

    = 217

  ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  11    217 nm
Each additional double bond

     +30

ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  12

Base: 217

+2×30

Each auxochromic alkyl group

      +5

           ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  13

 Base: 217                   +3×5

Each exocyclic double bond

      +5

                      ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  14

Base: 217

     + 5

Homoannular diene (both double bonds are situated in a ring)

    + 39

            ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  15

Base: 217

    +39

(d)

Interpretation Introduction

Interpretation:

The expected value for λmax of the given compounds should be determined by using Woodward-Fieser rule.

Concept introduction:

  • The π-systems of conjugated dienes absorb UV or visible light (200nm – 800nm).
  • The wavelength of maximum absorption of a compound is called λmax .
  • The value of λmax is highly depending on the extent of conjugation (number of conjugated double bonds).                                                                                                       Conjugated double bonds are the C=C bonds, which are separated by one σ-bond.
  • According to Woodward-Fieser rule, the portion of the molecule which absorbs UV-visible light is called chromophore and the groups attached to the chromophore are auxochromes. Woodward-Fieser rule gives the estimate value for λmax .
  • The estimate value for λmax are given in below table,
FEATURES λmax - value Example Calculation
Conjugated- diene

  Base value

    = 217

  ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  16    217 nm
Each additional double bond

     +30

ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  17

Base: 217

+2×30

Each auxochromic alkyl group

      +5

           ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  18

 Base: 217                   +3×5

Each exocyclic double bond

      +5

                      ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  19

Base: 217

     + 5

Homoannular diene (both double bonds are situated in a ring)

    + 39

            ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<, Chapter 17.11, Problem 29PTS , additional homework tip  20

Base: 217

    +39

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Students have asked these similar questions
#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv
Don't used Ai solution
I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."

Chapter 17 Solutions

ORG.CHEM EBOOK W/BBWILEY PLUS>CUSTOM<

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