Machine-translated by Google. Questions are authored in English.
Top

Discussion

Why does conjugation lower a carbonyl stretching frequency?

  • A.Delocalisation reduces the double bond character
  • B.Conjugation increases the reduced mass of the group
  • C.Conjugated carbonyls are more polar than isolated ones
  • D.The conjugated system absorbs some of the energy

Answer: A

Sharing electron density with the adjacent pi system gives the carbon-oxygen bond some single bond character, lowering its force constant and hence its frequency by twenty or thirty reciprocal centimetres. Reduced mass is unchanged, polarity affects intensity, and no energy is absorbed elsewhere. That a shift of a few tens of wavenumbers reports on the electronic environment is what makes the carbonyl band so informative beyond merely announcing that a carbonyl is present.

No comment is present. Be the first to comment.
Loading…

Post your comment

Please log in or register to post a comment.