Why are n-π* transitions generally of low intensities/low absorptions?

Macroscale and Microscale Organic Experiments
7th Edition
ISBN:9781305577190
Author:Kenneth L. Williamson, Katherine M. Masters
Publisher:Kenneth L. Williamson, Katherine M. Masters
Chapter56: The Synthesis Of 2,2-dimethyl-1,5-dioxolane; The Acetonide Derivative Of A Vicinal Diol
Section: Chapter Questions
Problem 5Q
icon
Related questions
Question
  1. Why are n-π* transitions generally of low intensities/low absorptions? 

  2. What photon energy and wavelength would you need to send on a compound having an energy gap (Eg) of 2.7 eV? Detail your answer with appropriate information.

  3.  Using molecular orbital theory/concept (draw the important molecular orbitals), explain the difference in absorption for the phenolphthalein in neutral medium or in basic medium, both for the n-π* and the π-π* transition. 

Expert Solution
steps

Step by step

Solved in 2 steps

Blurred answer
Knowledge Booster
Nuclear Magnetic Resonance
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Macroscale and Microscale Organic Experiments
Macroscale and Microscale Organic Experiments
Chemistry
ISBN:
9781305577190
Author:
Kenneth L. Williamson, Katherine M. Masters
Publisher:
Brooks Cole
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning