inductive effect and hyperconjugation -...
TRANSCRIPT
![Page 1: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/1.jpg)
Inductive effects and Hyperconjugation
![Page 2: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/2.jpg)
Inductive effects are electronic effects that occur through sigma σ bonds caused by electronegativity differences of atoms.
Electron donor groups (Z) stabilize a (+) charge; Z→Y+. Electron-withdrawing groups
(W) stabilize a (–) charge; W←Y –.
Inductive effects
![Page 3: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/3.jpg)
p208a
The following is a partial list of inductive electron-withdrawing groups:
In contrast, only a few groups are electron-donating relative to hydrogen because of their inductive effects. Two of these are electron rich because of their negatively charged oxygen atoms. In addition, alkyl groups, such as CH
3 and CH
2CH
3, behave as weak
electron-donating groups in many situations:
![Page 4: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/4.jpg)
Carbocation Stabilities
![Page 5: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/5.jpg)
Hyperconjugation
A second explanation for the observed trend in carbocation stability is based on orbital overlap. A 3° carbocation is more stable than a 2°, 1°, or methyl carbocation because the positive charge is delocalized over more than one atom.
Spreading out charge by the overlap of an empty p orbital with an adjacent σ bond is called hyperconjugation.
For examaple, CH3+ cannot be stabilized by hyperconjugation, but (CH3)2CH+ can:
![Page 6: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/6.jpg)
Chapter 4 6
Carbocation Stability (Continued)
• Stabilized by alkyl substituents in two ways:
1. Inductive effect: Donation of electron density along the sigma bonds.
2. Hyperconjugation: Overlap of sigma bonding orbitals with empty p orbital.
![Page 7: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/7.jpg)
Chapter 4 7
Carbon Reactive Intermediates
![Page 8: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/8.jpg)
Chapter 4 8
Carbocation Structure
• Carbon has 6 electrons, positively charged. • Carbon is sp2 hybridized with vacant p orbital.
![Page 9: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/9.jpg)
Carbocation Stabilities
![Page 10: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/10.jpg)
Chapter 4 10
Free Radicals
• Also electron-deficient. • Stabilized by alkyl substituents. • Order of stability:
3° > 2° > 1° > methyl
![Page 11: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/11.jpg)
Relative Stabilities of Alkyl Radicals
![Page 12: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/12.jpg)
Chapter 4 12
Carbanions
• Eight electrons on carbon: 6 bonding plus one lone pair.
• Carbon has a negative charge.
• Destabilized by alkyl substituents.
• Methyl >1° > 2 ° > 3 °
![Page 13: Inductive effect and Hyperconjugation - staff.du.edu.egstaff.du.edu.eg/upfilestaff/447/courses/8447_1457376704__Inductive.effect..pdf · The following is a partial list of inductive](https://reader033.vdocuments.pub/reader033/viewer/2022042012/5e72b991209df326511de1bc/html5/thumbnails/13.jpg)
Chapter 4 13
Carbenes
• Carbon is neutral. • Vacant p orbital, so can be electrophilic. • Lone pair of electrons, so can be nucleophilic.