November 25, 2024, 05:41:05 AM
Forum Rules: Read This Before Posting


Topic: Optically active molecules  (Read 3541 times)

0 Members and 1 Guest are viewing this topic.

Offline plankk

  • Full Member
  • ****
  • Posts: 150
  • Mole Snacks: +20/-4
  • Gender: Female
Optically active molecules
« on: July 27, 2009, 12:09:11 PM »
I have had a task to choose a molecules, which are optically active. According to the answer molecule (in attachment) has sterocenter and it is optically active. As far as I know the all subtituents should be different, and in that example we have two the same - methyl - susbtituents. So how could it be optically active?

Offline azmanam

  • Chemist
  • Sr. Member
  • *
  • Posts: 1416
  • Mole Snacks: +160/-24
  • Mediocrity is a handrail -Charles Louis d'Secondat
Re: Optically active molecules
« Reply #1 on: July 27, 2009, 12:12:22 PM »
you're right, it's not.  In general, tetrasubstitued amines can be optically active if a) all four substituents are different and b) the amine cannot invert easily (i.e. the 4th substituent is usually not a proton)
Knowing why you got a question wrong is better than knowing that you got a question right.

Offline plankk

  • Full Member
  • ****
  • Posts: 150
  • Mole Snacks: +20/-4
  • Gender: Female
Re: Optically active molecules
« Reply #2 on: July 27, 2009, 03:56:27 PM »
Thanks a lot.

Sponsored Links