Search Results
| Search type | Search syntax |
|---|---|
| Tags | [tag] |
| Exact | "words here" |
| Author |
user:1234 user:me (yours) |
| Score |
score:3 (3+) score:0 (none) |
| Answers |
answers:3 (3+) answers:0 (none) isaccepted:yes hasaccepted:no inquestion:1234 |
| Views | views:250 |
| Code | code:"if (foo != bar)" |
| Sections |
title:apples body:"apples oranges" |
| URL | url:"*.example.com" |
| Saves | in:saves |
| Status |
closed:yes duplicate:no migrated:no wiki:no |
| Types |
is:question is:answer |
| Exclude |
-[tag] -apples |
| For more details on advanced search visit our help page | |
Results tagged with enolate-chemistry
Search options questions only
not deleted
user 91756
Enolates are anions derived from the deprotonation of carbonyl compounds. This tag must be used while dealing with the enolates or its derivatives including its resonance forms.
1
vote
1
answer
116
views
Why can't the N- end of the nitrile anion attack the alkyl halide in an SN2 fashion during a...
I'm reading my Clayden textbook and something keeps nagging me. It says that when we're carrying out alkylation reactions with an enol attacking an alkyl halide with strong base catalysis (with hydrox …
- 129