Hyperconjugation effect
- 1. PT. MOHAN LAL SD COLLEGE FOR WOMEN, GURDASPUR Class- B.Sc SemI Subject – Organic Cemistry Chapter Name – Structure and Bonding Topic – Hyperconjugation Effect Submitted By – Mrs. Gurdeep kaur Asst. Prof. in Chemistry
- 2. WHAT IS HYPERCONJUGATION EFFECT When alkyl groups are attached to an unsaturated system like double bond or a benzene ring, the +I –effect is reversed. This effect is called hyperconjugation.
- 3. ORBITAL CONCEPT Hyper conjugation involves delocalization of σ-electrons through overlapping of p-orbitals of the double bond with σ-orbital of the adjacent single bond . It is also known as σ- π-conjugation or Baker-Nathan effect or no bond resonance.
- 6. SIGNIFICANCE OF HYPERCONJUGATION Directive influence of alkyl groups:- Alkyl groups are o,p-directing in nature because as a result of hyperconjugation, the electron density at o- and p- positions w.r.t the CH3 group increases and hence electrophilic substitution reactions in toluene will occur at o- and p- positions w.r.t the CH3
- 7. 1) Stability of alkenes: The stability of alkenes increases with increase in the number of alkyl groups (containing hydrogens) on the double bond. It is due to increase in the number of contributing no bond resonance structures. For example, 2-butene is more stable than 1-butene. This is because in 2-butene, there are six hydrogens involved in hyperconjugation whereas there are only two hydrogens involved in case of 1-butene. Hence the contributing structures in 2-butene are more and is more stable than 1-butene.
- 8. The increasing order of stability of alkenes with increases in the number of methyl groups on the double bond is depicted below. This order is supported by the heat of hydrogenation data of these alkenes. The values of heats of hydrogenation decrease with increase in the stability of alkenes. Also the heats of formation of more substituted alkenes are higher than expected. .
- 9. It is important to note that the alkyl groups attached to the double bond must contain at least one hydrogen atom for hyperconjugation. For example, in case of the following alkene containing a tert-butyl group on doubly bonded carbon, the hyperconjugation is not possible
- 10. However propene is more stable than 1-butene. This is because there are three hydrogens on α- methyl group involved in hyperconjugation. Whereas, in 1-butene there are only two hydrogen atoms on -CH2 group that can take part in hyperconjugation.
- 11. 2) Stability of carbocations :- The ethyl carbocation, CH3-CH2 + is more stable than the methyl carbocation, CH3 +. This is because, the σ- electrons of the α-C-H bond in ethyl group are delocalized into the empty p-orbital of the positive carbon center and thus by giving rise to 'no bond resonance structures' as shown below. Whereas hyperconjugation is not possible in methyl carbocation and hence is less stable.
- 12. The stability of carbonium ions increases with increase in the number of alkyl groups attached to the positively charged carbon due to increase in the number of contributing structures to hyperconjugation.
- 13. Thus the increasing order of stability of carbocations can be given as: methyl < primary < secondary < tertiary
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