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INVESTIGATIONS IN THE BICYCLOHEPTANE SERIES: PART I. THE ELECTRONIC EFFECT OF METHYL GROUPS ON C6 OF THE NORBORNYL CATION
The addition of acetic acid to camphenilene has been carried out. The major products are the two expected from normal addition without rearrangement. From the product ratio it is possible to conclude that the difference between the electronic effect of a methyl and a hydrogen at C 6 of the norbornyl...
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Published in: | Canadian journal of chemistry 1962-08, Vol.40 (8), p.1554-1558 |
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container_end_page | 1558 |
container_issue | 8 |
container_start_page | 1554 |
container_title | Canadian journal of chemistry |
container_volume | 40 |
creator | McGreer, Donald E |
description | The addition of acetic acid to camphenilene has been carried out. The major products are the two expected from normal addition without rearrangement. From the product ratio it is possible to conclude that the difference between the electronic effect of a methyl and a hydrogen at C
6
of the norbornyl cation is small. |
doi_str_mv | 10.1139/v62-234 |
format | article |
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6
of the norbornyl cation is small.</description><identifier>ISSN: 0008-4042</identifier><identifier>EISSN: 1480-3291</identifier><identifier>DOI: 10.1139/v62-234</identifier><language>eng</language><publisher>Ottawa, Canada: NRC Research Press</publisher><ispartof>Canadian journal of chemistry, 1962-08, Vol.40 (8), p.1554-1558</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>McGreer, Donald E</creatorcontrib><title>INVESTIGATIONS IN THE BICYCLOHEPTANE SERIES: PART I. THE ELECTRONIC EFFECT OF METHYL GROUPS ON C6 OF THE NORBORNYL CATION</title><title>Canadian journal of chemistry</title><addtitle>Revue canadienne de chimie</addtitle><description>The addition of acetic acid to camphenilene has been carried out. The major products are the two expected from normal addition without rearrangement. From the product ratio it is possible to conclude that the difference between the electronic effect of a methyl and a hydrogen at C
6
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6
of the norbornyl cation is small.</abstract><cop>Ottawa, Canada</cop><pub>NRC Research Press</pub><doi>10.1139/v62-234</doi><tpages>5</tpages></addata></record> |
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issn | 0008-4042 1480-3291 |
language | eng |
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source | EZB-FREE-00999 freely available EZB journals |
title | INVESTIGATIONS IN THE BICYCLOHEPTANE SERIES: PART I. THE ELECTRONIC EFFECT OF METHYL GROUPS ON C6 OF THE NORBORNYL CATION |
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