Mendelejev Posted May 20, 2005 Share Posted May 20, 2005 Could someone explain me the following : I made a TLC of three amino acids : glycine, leucine and aspartic acid. I used a ethanol-water-ammonia (25%) solution (8 parts ethanol, 1 part water and 1 part ammonia). My calculated Rf values were quite similar with those found on internet : aspartic acid : 0,24 glycine : 0,26 leucine : 0,73 But why does leucine go so high ??? Aspartic acid is the most polar, so i would think it would have the highest Rf value becouse my solution is also polar. Glycine with R = H is less polar, but leucine is quite apolar becouse R = (CH3)2-CH-CH2- ! So it would be logical that leucine would have the smalles Rf-value. Could someone explain me why it's just the opposite of what I've just said ??? Link to comment Share on other sites More sharing options...
Recommended Posts
Create an account or sign in to comment
You need to be a member in order to leave a comment
Create an account
Sign up for a new account in our community. It's easy!
Register a new accountSign in
Already have an account? Sign in here.
Sign In Now