Khyati Posted October 3, 2010 Share Posted October 3, 2010 1)Why can the use of high temperatures in the catalytic hydrogenation of alkenes to alkanes be self-defeating ? 2)We know that if the substituent is present at the equatorial position in cyclohexane then that compound is more stable, then why all trans-1,2,3,4,5,6-Hexaisopropylcyclohexane is a stable molecule in which all isopropyl groups are axial ? 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