Jump to content

Recommended Posts

Posted

Hello everyone,

 

1. As you increase alkalinity of the solution open chain form of monosaccharides increase. I like to know the chemical reason behind this.

2. Aldehydes oxidize things more than Ketones. I know that this is due to the hyrdogen atom but how does that make aldehydes more reactive. Isn't oxygen in ketone a strong oxidizing agent?

3. What happens to monosaccharides in the presence of acid?

 

Thanks for the help :)

  • 2 weeks later...
Posted

About your question of alkalinity helps opening up of ring form, would it be possible to be related to deprotonation of hydroxyl group on C1 favoring cleavage of COC bond?

If this is a possibility, will acidic condition protonate hydroxyl group on C5, also favoring ring opening?

  • 2 weeks later...

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 account

Sign in

Already have an account? Sign in here.

Sign In Now
×
×
  • Create New...

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.