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INVESTIGATIONS IN THE BICYCLOHEPTANE SERIES: PART I. THE ELECTRONIC EFFECT OF METHYL GROUPS ON C 6 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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Language: | English |
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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
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6
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6
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title | INVESTIGATIONS IN THE BICYCLOHEPTANE SERIES: PART I. THE ELECTRONIC EFFECT OF METHYL GROUPS ON C 6 OF THE NORBORNYL CATION |
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