- #1
member 392791
Hello, I am wondering...
If you have two ethylenediamines (en) oriented in a cis en-en fashion, will they always have an optical isomer? I have not found a case yet where they do, and it would probably save time to assume optically active in an environment presseed for time (such as on a test) Thanks.
If you have two ethylenediamines (en) oriented in a cis en-en fashion, will they always have an optical isomer? I have not found a case yet where they do, and it would probably save time to assume optically active in an environment presseed for time (such as on a test) Thanks.