Jump to content

Catalytic Hydrogenation and stability

Featured Replies

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 ?

Archived

This topic is now archived and is closed to further replies.

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.

Configure browser push notifications

Chrome (Android)
  1. Tap the lock icon next to the address bar.
  2. Tap Permissions → Notifications.
  3. Adjust your preference.
Chrome (Desktop)
  1. Click the padlock icon in the address bar.
  2. Select Site settings.
  3. Find Notifications and adjust your preference.