ORGANIC CHEMISTRY-OWL V2 ACCESS
ORGANIC CHEMISTRY-OWL V2 ACCESS
8th Edition
ISBN: 9781305582422
Author: Brown
Publisher: CENGAGE L
Question
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Chapter 20.3, Problem 20.4P

(a)

Interpretation Introduction

Interpretation: The given conversion has to be carried out:

Concept Introduction:

UV- spectroscopy :

  • UV- spectroscopy is the technique that is widely used to characterize a compound via conjugation.
  • • Conjugation between double bonds in a compound decreases the energy gap between filled and unfilled π-orbitals.
  • • The smaller energy gap absorbs longer wavelength of ultraviolet radiation and effectively promotes the π-π* transition.
  • • The longer wavelength of UV- radiation can be easily observed in UV- spectroscopy which corresponds to the particular π-π* transition of conjugation.
  • • By this way, UV- spectroscopy characterizes a compound with conjugation.

Example for the conversion of wavelength from μm to nm is shown here:

Let a wavelength has the value as x in the units of μm.

wavelength=xμm

1μm=1000nm1000nm1μm×xμm=x×103nm

(b)

Interpretation Introduction

Interpretation: The given conversion has to be carried out:

Concept Introduction:

UV- spectroscopy :

  • UV- spectroscopy is the technique that is widely used to characterize a compound via conjugation.
  • • Conjugation between double bonds in a compound decreases the energy gap between filled and unfilled π-orbitals.
  • • The smaller energy gap absorbs longer wavelength of ultraviolet radiation and effectively promotes the π-π* transition.
  • • The longer wavelength of UV- radiation can be easily observed in UV- spectroscopy which corresponds to the particular π-π* transition of conjugation.
  • • By this way, UV- spectroscopy characterizes a compound with conjugation.

Example for the conversion of wavelength from nm to μm is shown here:

Let a wavelength has the value as x in the units of nm.

wavelength=xnm

1μm=1000nm1μm1000nm×xnm=x×103μm

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Chapter 20 Solutions

ORGANIC CHEMISTRY-OWL V2 ACCESS

Ch. 20.6 - Prob. 20.11PCh. 20.6 - Prob. 20.12PCh. 20 - If an electron is added to 1,3-butadiene, into...Ch. 20 - Prob. 20.15PCh. 20 - Predict the structure of the major product formed...Ch. 20 - Predict the major product formed by 1,4-addition...Ch. 20 - Predict the structure of the major 1,2-addition...Ch. 20 - Prob. 20.19PCh. 20 - Prob. 20.20PCh. 20 - Prob. 20.21PCh. 20 - Prob. 20.22PCh. 20 - Prob. 20.23PCh. 20 - Pyridine exhibits a UV transition of the type n at...Ch. 20 - Prob. 20.25PCh. 20 - Prob. 20.26PCh. 20 - Prob. 20.27PCh. 20 - Write the frontier molecular orbital analysis for...Ch. 20 - Prob. 20.29PCh. 20 - Draw structural formulas for the products of...Ch. 20 - Propose structural formulas for compounds A and B...Ch. 20 - Under certain conditions, 1,3-butadiene can...Ch. 20 - Prob. 20.33PCh. 20 - Prob. 20.34PCh. 20 - The following triene undergoes an intramolecular...Ch. 20 - Prob. 20.36PCh. 20 - Prob. 20.37PCh. 20 - Prob. 20.38PCh. 20 - Prob. 20.39PCh. 20 - The Diels-Alder reaction is not limited to making...Ch. 20 - The first step in a synthesis of dodecahedrane...Ch. 20 - Bicyclo-2,5-heptadiene can be prepared in two...Ch. 20 - Prob. 20.43PCh. 20 - Prob. 20.44PCh. 20 - Following is a retrosynthetic scheme for the...Ch. 20 - Prob. 20.46PCh. 20 - Prob. 20.47PCh. 20 - Prob. 20.48PCh. 20 - Prob. 20.49PCh. 20 - Prob. 20.50PCh. 20 - What reaction presented in this chapter is...Ch. 20 - Claisen rearrangement of an allyl phenyl ether...Ch. 20 - Prob. 20.53PCh. 20 - Prob. 20.54PCh. 20 - We now continue the use of organic chemistry...Ch. 20 - Write the products of the following sequences of...
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