Chemistry Homework Solutions
Problem
#47474

synthesis of trans -9-(2-phenylethenyl) anthracene

In synthesis of trans-9-(2-phenylethenyl) anthracene a carbonyl group is converted to a benzylidene group by reaction with the ylide derived from benzyltriphenylphosphorium chloride.  Would it have been possible to use the ylide derived from benzyltrimethylphosphonium chloride in this reaction?  Answer the same question for the case in which benzyl is replaced by ethyl.  What is involved?

Solution
What is this?
By OTA - Overall OTA Rating
Siva Kumar, MSc, MPhil - 4.5/5
Purchase Cost Now
$2.19 CAD (was ~$11.97)
Included in Download
  • Plain text response
  • Attached file(s):
    • 47474_soln1.jpg
    • 47474_soln2.jpg
    • 47474_soln3.jpg
    • 47474_soln4.jpg
$2.19 Instant Download
Add to Cart
Why you can trust BrainMass.com
  • Your Information is Secure
  • Best Online Academic Help Service
  • Students find real academic Success
Related Solutions
  • Diels-Alder Adduct - Offer an explanation of why anthracene preferentially forms a Diels-Alder adduct at 9,10 positions.
  • Resonance Structures for Anthracene - There are four reasonable resonance structures for anthracene. Draw them.
  • 2 Questions (L4) - 1. Offer an explanation of why anthracene preferentially forms a Diels-Alder adduct at 9,10 positions. 4. Outline a synthetic reaction scheme for the preparation of triphenylmethanol from: a. Me ...
  • Questions #2 and #3 (L4) - 2. There are four reasonable resonance structures for anthracene. Draw them. 3. A large number of polycyclic benzenoid aromatic hydrocarbons are known. One of these, benz/a/pyrene, is a powerful ca ...
  • anthracene - Offer an explanation of why anthracene preferentially forms a Diels-Alder adduct at 9,10 positions. Draw the resonance structures for anthracene.
Browse