The kinetics of the thermal gas‐phase reaction Br 2 + C 6 F 5 I → BrI + C 6 F 5 Br. An attempt to determine the bond dissociation energy D (C 6 F 5 ‐I)
The kinetics of the thermal bromination reaction equation image have been studied in the range of 261°–391°C. The observed rate law is compatible with initiation by the step equation image for which we obtain where Θ = 2.303 RT cal/mol. Using the above value of E 6 , we have This result disagrees wi...
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Veröffentlicht in: | International journal of chemical kinetics 1978-06, Vol.10 (6), p.591-598 |
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creator | Okafo, Ernest N. Whittle, Eric |
description | The kinetics of the thermal bromination reaction
equation image
have been studied in the range of 261°–391°C. The observed rate law is compatible with initiation by the step
equation image
for which we obtain
where Θ = 2.303
RT
cal/mol. Using the above value of
E
6
, we have
This result disagrees with values of
D
(C
6
F
5
‐I) obtained in other ways and we conclude that reaction (3) probably does not involve initiation by reaction (6). Instead, initiation may involve an addition of Br to the ring in C
6
F
5
I followed by decomposition of the adduct to give C
6
F
5
Br. If correct, this implies that the Arrhenius parameters above refer to the addition reaction rather than to reaction (6). |
doi_str_mv | 10.1002/kin.550100606 |
format | Article |
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equation image
have been studied in the range of 261°–391°C. The observed rate law is compatible with initiation by the step
equation image
for which we obtain
where Θ = 2.303
RT
cal/mol. Using the above value of
E
6
, we have
This result disagrees with values of
D
(C
6
F
5
‐I) obtained in other ways and we conclude that reaction (3) probably does not involve initiation by reaction (6). Instead, initiation may involve an addition of Br to the ring in C
6
F
5
I followed by decomposition of the adduct to give C
6
F
5
Br. If correct, this implies that the Arrhenius parameters above refer to the addition reaction rather than to reaction (6).</description><identifier>ISSN: 0538-8066</identifier><identifier>EISSN: 1097-4601</identifier><identifier>DOI: 10.1002/kin.550100606</identifier><language>eng</language><ispartof>International journal of chemical kinetics, 1978-06, Vol.10 (6), p.591-598</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c826-45ffc5411c8e7122f8cbda69b306a00e048b04a0a4053425bf4e4cdf695007f03</citedby><cites>FETCH-LOGICAL-c826-45ffc5411c8e7122f8cbda69b306a00e048b04a0a4053425bf4e4cdf695007f03</cites></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>Okafo, Ernest N.</creatorcontrib><creatorcontrib>Whittle, Eric</creatorcontrib><title>The kinetics of the thermal gas‐phase reaction Br 2 + C 6 F 5 I → BrI + C 6 F 5 Br. An attempt to determine the bond dissociation energy D (C 6 F 5 ‐I)</title><title>International journal of chemical kinetics</title><description>The kinetics of the thermal bromination reaction
equation image
have been studied in the range of 261°–391°C. The observed rate law is compatible with initiation by the step
equation image
for which we obtain
where Θ = 2.303
RT
cal/mol. Using the above value of
E
6
, we have
This result disagrees with values of
D
(C
6
F
5
‐I) obtained in other ways and we conclude that reaction (3) probably does not involve initiation by reaction (6). Instead, initiation may involve an addition of Br to the ring in C
6
F
5
I followed by decomposition of the adduct to give C
6
F
5
Br. If correct, this implies that the Arrhenius parameters above refer to the addition reaction rather than to reaction (6).</description><issn>0538-8066</issn><issn>1097-4601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><recordid>eNpNkLtOwzAUhi0EEqUwsp8RhBKOE9tJxl4oRKrE0j1yHLsNtElle-nGxIzYebk-CaZcxHB0LtL5fukj5JJiTBGT2-e2iznHMAsUR2RAscgiJpAekwHyNI9yFOKUnDn3hIhFQfmAfCxWGsKj9q1y0BvwYQ9lN3INS-n2L2_blXQarJbKt30HYwsJ3MAEBMyAQwn71_dwLP_dxjaGUQfSe73ZevA9NNoHZIg58Ou-a6BpnetVKw9Q3Wm73MEUrn4ZIbi8PicnRq6dvvjpQ7KY3S0mD9H88b6cjOaRyhMRMW6M4oxSleuMJonJVd1IUdQpComokeU1MomSBQss4bVhmqnGiIIjZgbTIYm-scr2zlltqq1tN9LuKorVl9oqGKr-1KafFF9ptA</recordid><startdate>197806</startdate><enddate>197806</enddate><creator>Okafo, Ernest N.</creator><creator>Whittle, Eric</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>197806</creationdate><title>The kinetics of the thermal gas‐phase reaction Br 2 + C 6 F 5 I → BrI + C 6 F 5 Br. An attempt to determine the bond dissociation energy D (C 6 F 5 ‐I)</title><author>Okafo, Ernest N. ; Whittle, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c826-45ffc5411c8e7122f8cbda69b306a00e048b04a0a4053425bf4e4cdf695007f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okafo, Ernest N.</creatorcontrib><creatorcontrib>Whittle, Eric</creatorcontrib><collection>CrossRef</collection><jtitle>International journal of chemical kinetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okafo, Ernest N.</au><au>Whittle, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The kinetics of the thermal gas‐phase reaction Br 2 + C 6 F 5 I → BrI + C 6 F 5 Br. An attempt to determine the bond dissociation energy D (C 6 F 5 ‐I)</atitle><jtitle>International journal of chemical kinetics</jtitle><date>1978-06</date><risdate>1978</risdate><volume>10</volume><issue>6</issue><spage>591</spage><epage>598</epage><pages>591-598</pages><issn>0538-8066</issn><eissn>1097-4601</eissn><abstract>The kinetics of the thermal bromination reaction
equation image
have been studied in the range of 261°–391°C. The observed rate law is compatible with initiation by the step
equation image
for which we obtain
where Θ = 2.303
RT
cal/mol. Using the above value of
E
6
, we have
This result disagrees with values of
D
(C
6
F
5
‐I) obtained in other ways and we conclude that reaction (3) probably does not involve initiation by reaction (6). Instead, initiation may involve an addition of Br to the ring in C
6
F
5
I followed by decomposition of the adduct to give C
6
F
5
Br. If correct, this implies that the Arrhenius parameters above refer to the addition reaction rather than to reaction (6).</abstract><doi>10.1002/kin.550100606</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0538-8066 |
ispartof | International journal of chemical kinetics, 1978-06, Vol.10 (6), p.591-598 |
issn | 0538-8066 1097-4601 |
language | eng |
recordid | cdi_crossref_primary_10_1002_kin_550100606 |
source | Wiley Online Library Journals Frontfile Complete |
title | The kinetics of the thermal gas‐phase reaction Br 2 + C 6 F 5 I → BrI + C 6 F 5 Br. An attempt to determine the bond dissociation energy D (C 6 F 5 ‐I) |
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