Timeline for Cyclopentanone is treated with piperidine
Current License: CC BY-SA 4.0
10 events
| when toggle format | what | by | license | comment | |
|---|---|---|---|---|---|
| Jun 1, 2020 at 16:05 | vote | accept | Yashwini | ||
| Jun 1, 2020 at 16:05 | vote | accept | Yashwini | ||
| Jun 1, 2020 at 16:05 | |||||
| Jun 1, 2020 at 16:00 | comment | added | Waylander | Exactly so, you regenerate the ketone | |
| Jun 1, 2020 at 15:56 | answer | added | Thenard Rinmann | timeline score: 3 | |
| Jun 1, 2020 at 15:55 | comment | added | Mathew Mahindaratne | Structure given for (B) is not quite correct. Your question says "(A) on reaction with benzyl bromide followed by hydrolysis gives another organic product (B)." Then what happens to the hydrolysis? | |
| Jun 1, 2020 at 15:51 | comment | added | Yashwini | A ketone with some extra carbons than the enolate! | |
| Jun 1, 2020 at 15:50 | comment | added | Mathew Mahindaratne | If you have a enolate and alkyl halide in a mixture, what product you expect to have? | |
| Jun 1, 2020 at 15:49 | history | edited | Yashwini | CC BY-SA 4.0 |
added 184 characters in body
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| Jun 1, 2020 at 15:47 | comment | added | user55119 | What reactions do enamines undergo? They are isoelectronic with enolates. | |
| Jun 1, 2020 at 15:43 | history | asked | Yashwini | CC BY-SA 4.0 |