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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kumar, D Santhosh | - |
| dc.contributor.author | Balachandran, S | - |
| dc.date.accessioned | 2009-12-09T11:07:18Z | - |
| dc.date.available | 2009-12-09T11:07:18Z | - |
| dc.date.issued | 2006-12 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6785 | - |
| dc.description | 2751-2753 | en_US |
| dc.description.abstract | 1-Chloro-1-(4-methoxyphenyl)-2-phenylethane undergoes dehydrochlorination in acetonitrile to give trans-p-methoxy stilbene by E1 mechanism. The presence of electron donating p-methoxy group and the delocalisation of charge throughout the structure proposes a stable cation. The mass law effect and special salt effect are characteristic for a reaction involving the stable cation and these effects have been reported for the first time in a pure E1 reaction. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.8 C07D | en_US |
| dc.source | IJC-B Vol.45B(12) December 2006] | en_US |
| dc.subject | Kinetic study | en_US |
| dc.subject | elimination reaction | en_US |
| dc.subject | dehydrochl-orination | en_US |
| dc.subject | phenylethane | en_US |
| dc.subject | trans-p-methoxy stilbene | en_US |
| dc.subject | acetonitrile | en_US |
| dc.title | Kinetics of elimination reactions of 1-chloro-1-(4-methoxyphenyl)-2-phenylethane in acetonitrile | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(12) December 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(12) 2751-2753.pdf | 149.33 kB | Adobe PDF | View/Open |
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