Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine
The relative reactivities of nuclear-substituted diphenylmethanes, deoxybenzoins (X·C6H4·CH2Bz), and allylbenzenes towards atomic bromine at 80° have been determined by means of competitive reactions by use of allylbenzene, diphenylmethyl methyl ether, and p-bromoethylbenzene, respectively, as refer...
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Royal Society of Chemistry
1970
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my.um.eprints.246152021-03-09T04:28:51Z http://eprints.um.edu.my/24615/ Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine Low, T.P. Lee, K.H. Q Science (General) QD Chemistry The relative reactivities of nuclear-substituted diphenylmethanes, deoxybenzoins (X·C6H4·CH2Bz), and allylbenzenes towards atomic bromine at 80° have been determined by means of competitive reactions by use of allylbenzene, diphenylmethyl methyl ether, and p-bromoethylbenzene, respectively, as reference standard. The results show p-values of -0.93, -0.92, and -0.68 by the Hammett equation for the three systems, the first two systems being better correlated by σ-constants while in the third system σ+-constants gave better correlation in agreement with a previous report. The probable reasons for the correlation with σ-constants are discussed. The ρ-values for these systems fit in well with the consistent inverse relationship with the reactivity values previously observed. Royal Society of Chemistry 1970 Article PeerReviewed Low, T.P. and Lee, K.H. (1970) Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine. Journal of the Chemical Society B: Physical Organic. pp. 535-538. ISSN 0045-6470 https://doi.org/10.1039/J29700000535 doi:10.1039/J29700000535 |
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Q Science (General) QD Chemistry Low, T.P. Lee, K.H. Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
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The relative reactivities of nuclear-substituted diphenylmethanes, deoxybenzoins (X·C6H4·CH2Bz), and allylbenzenes towards atomic bromine at 80° have been determined by means of competitive reactions by use of allylbenzene, diphenylmethyl methyl ether, and p-bromoethylbenzene, respectively, as reference standard. The results show p-values of -0.93, -0.92, and -0.68 by the Hammett equation for the three systems, the first two systems being better correlated by σ-constants while in the third system σ+-constants gave better correlation in agreement with a previous report. The probable reasons for the correlation with σ-constants are discussed. The ρ-values for these systems fit in well with the consistent inverse relationship with the reactivity values previously observed. |
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Article |
author |
Low, T.P. Lee, K.H. |
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Low, T.P. Lee, K.H. |
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Low, T.P. |
title |
Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
title_short |
Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
title_full |
Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
title_fullStr |
Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
title_full_unstemmed |
Polar influences in radical reactions. Part VII. Hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
title_sort |
polar influences in radical reactions. part vii. hydrogen abstraction from nuclear-substituted diphenylmethanes, deoxybenzoins, and allylbenzenes by atomic bromine |
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Royal Society of Chemistry |
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1970 |
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http://eprints.um.edu.my/24615/ https://doi.org/10.1039/J29700000535 |
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1695531096037392384 |
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13.251813 |