Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Locant
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
===Enols and enolates=== The Ξ±-carbon is important for [[enol]]- and [[enolate]]-based [[carbonyl]] chemistry as well. Chemical transformations affected by the conversion to either an enolate or an enol, in general, lead to the Ξ±-carbon acting as a [[nucleophile]], becoming, for example, [[alkylated]] in the presence of primary [[haloalkane]]. An exception is in reaction with [[silyl]] [[chlorosilane|chlorides]], [[bromide]]s, and [[iodide]]s, where the [[oxygen]] acts as the nucleophile to produce [[silyl enol ether]].
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)