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 hyperconjugation
Search options not deleted
user 95340
Hyperconjugation involves the donation of electrons from a filled orbital (commonly the bonding C-H sigma molecular orbital) into an adjacent/partially occupied p-orbital (for instance an adjacent carbocation) leading to stabilisation. The tag should be applied to questions where hyperconjugation is involved, even if the question does not explicitly refer to it.
8
votes
Accepted
How to compare stability between 5‐methylcyclohexa‐1,3‐diene and 3‐methylenecyclohexene?
As far as I have read, in general, exocyclic double bonds (which are outside the ring) are stable for 3 or 4 numbered rings while endocyclic double bonds (which are inside the ring) are stable in 5 or …
- 7,050