Radicals masquerading as electrophiles - 7 Angebote vergleichen
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Radicals masquerading as electrophiles (2015)
DE PB NW RPISBN: 9783639668711 bzw. 3639668715, in Deutsch, SPS Feb 2015, Taschenbuch, neu, Nachdruck.
Von Händler/Antiquariat, AHA-BUCH GmbH [51283250], Einbeck, Germany.
This item is printed on demand - Print on Demand Titel. Neuware - This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 320 pp. Englisch.
This item is printed on demand - Print on Demand Titel. Neuware - This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 320 pp. Englisch.
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Radicals masquerading as electrophiles
DE PB NWISBN: 9783639668711 bzw. 3639668715, in Deutsch, Scholar'S Press, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
buecher.de GmbH & Co. KG, [1].
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.2015. 320 S. 220 mmVersandfertig in 3-5 Tagen, Softcover.
buecher.de GmbH & Co. KG, [1].
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.2015. 320 S. 220 mmVersandfertig in 3-5 Tagen, Softcover.
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Symbolbild
Radicals Masquerading as Electrophiles (Paperback) (2015)
DE PB NW RPISBN: 9783639668711 bzw. 3639668715, in Deutsch, Scholars Press, United States, Taschenbuch, neu, Nachdruck.
Lieferung aus: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, The Book Depository EURO [60485773], Slough, United Kingdom.
Language: English Brand New Book ***** Print on Demand *****.This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.
Von Händler/Antiquariat, The Book Depository EURO [60485773], Slough, United Kingdom.
Language: English Brand New Book ***** Print on Demand *****.This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.
4
Symbolbild
Radicals masquerading as electrophiles (2016)
~EN PB NWISBN: 9783639668711 bzw. 3639668715, vermutlich in Englisch, SPS Aug 2016, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, BuchWeltWeit Inh. Ludwig Meier e.K. [57449362], Bergisch Gladbach, Germany.
Neuware - This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may dominate. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 320 pp. Englisch.
Von Händler/Antiquariat, BuchWeltWeit Inh. Ludwig Meier e.K. [57449362], Bergisch Gladbach, Germany.
Neuware - This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may dominate. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 320 pp. Englisch.
5
Radicals masquerading as electrophiles
DE NWISBN: 9783639668711 bzw. 3639668715, in Deutsch, VDM Verlag Dr. Müller, Saarbrücken, Deutschland, neu.
Lieferung aus: Deutschland, zzgl. Versandkosten.
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may ***te. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles.
6
Radicals masquerading as electrophiles - Exploring frontier orbital interactions in free radical reactions (2015)
~EN PB NWISBN: 9783639668711 bzw. 3639668715, vermutlich in Englisch, 320 Seiten, Scholar's Press, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkosten nach: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, Syndikat Buchdienst, [4235284].
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may dominate. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 2015, Taschenbuch / Paperback, Neuware, H: 220mm, B: 150mm, T: 16mm, 441g, 320, Internationaler Versand, Selbstabholung und Barzahlung, PayPal, offene Rechnung, Banküberweisung.
Von Händler/Antiquariat, Syndikat Buchdienst, [4235284].
This work was undertaken to gain insights into mechanistic pathways in radical addition reactions. The multicomponent orbital interactions observed in this study revealed that the radical centre may not be the only or the most reacting centre in the free radical moiety. Contrary to widespread belief, radicals may be subjected to the same driving forces that operate during nucleophile-electrophile reactions. It appears that the charge transfer interaction between the radical and substrate will depend on the electrophilicity of the radical and charges operating during the reaction phase. In the reactions of radicals with strong electrophilic character, where charge separation exists in the transition state, coulombic interactions may dominate. In this instance neglect of charges can lead to misleading results. The orbital interactions observed in this study appear to have a profound effect on the geometry of the reacting systems. Two reacting moieties tend to orient themselves in such a way so as to maximize the energy gained through all possible orbital interactions. This is the principal factor in site specific reactions between electrophiles and nucleophiles. 2015, Taschenbuch / Paperback, Neuware, H: 220mm, B: 150mm, T: 16mm, 441g, 320, Internationaler Versand, Selbstabholung und Barzahlung, PayPal, offene Rechnung, Banküberweisung.
7
Radicals masquerading as electrophiles
EN NWISBN: 9783639668711 bzw. 3639668715, in Englisch, OmniScriptum GmbH & Co. KG, OmniScriptum GmbH & Co. KG, neu.
Lieferung aus: Vereinigte Staaten von Amerika, zzgl. Versandkosten, Free Shipping on eligible orders over $25.
Sambor Ina, Paperback, English-language edition, Pub by OmniScriptum GmbH & Co. KG.
Sambor Ina, Paperback, English-language edition, Pub by OmniScriptum GmbH & Co. KG.
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