Following is a retrosynthetic analysis for the synthesis of the herbicide

Chapter 18, Problem 18.49

(choose chapter or problem)

Following is a retrosynthetic analysis for the synthesis of the herbicide (S)-Metolachlorfrom 2-ethyl-6-methylaniline, chloroacetic acid, acetone, and methanol. Show reagents and experimental conditions for the synthesis of Metolachlor from thesefour organic starting materials. Your synthesis will most likely give a racemic mixture.The chiral catalyst used by Novartis for reduction in Step 2 gives 80% enantiomeric ex-cess of the S enantiomer.

Unfortunately, we don't have that question answered yet. But you can get it answered in just 5 hours by Logging in or Becoming a subscriber.

Becoming a subscriber
Or look for another answer

×

Login

Login or Sign up for access to all of our study tools and educational content!

Forgot password?
Register Now

×

Register

Sign up for access to all content on our site!

Or login if you already have an account

×

Reset password

If you have an active account we’ll send you an e-mail for password recovery

Or login if you have your password back