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Dr. Mohd Kamil Hussain
Department of Chemistry
Govt. Raza P.G. College Rampur, U.P. India
Hyperconjugation
Lockdown
222
Hyperconjugation
The delocalization of σ-electron in to adjacent π orbital or p-orbital is called hyperconjugation. The contributing
structures involving sigma electrons of C - H bond do not show any covalent bond between C and H.
Hyperconjugation, therefore, is also called as "no bond resonance" or "Baker-Nathan effect
Dr. Mohd Kamil Hussain
Requirements for Hyperconjugation:
There must be an α-C-H group or a lone pair on atom adjacent to sp2 hybrid carbon or other atoms like nitrogen, oxygen etc.
Alkenes, alkyl carbocations, alkyl free radicals, nitro compounds with α- hydrogen.
33
Consequences and Applications of Hyperconjugation
Dr. Mohd Kamil Hussain
•Stability of alkenes
As a general rule, greater the number of α-H of alkyl group attached on the double bond greater is the stability of
alkene. With rise in the stability of alkene, the value of heat of hydrogenation deceases
Dr. Mohd Kamil Hussain
Stability of carbocations :
In general, As the number of α-H of alkyl group attached to the positively charged carbon increases, the stability of carbonium ions
increases because of increase in the number of contributing structures to hyperconjugation contributing structures to hyperconjugation.
Thus the increasing order of stability of carbocations can be given as:
methyl < primary < secondary < tertiary as depicted below
5
Stability of free radicals
The stability of free radicals is influenced by hyperconjugation just as in case of carbonium ions. Due to hyperconjugation, the
stability of free radicals also follow the same order as that of carbonium ions
i.e., methyl < primary < secondary < tertiary

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Hyperconjugation

  • 1. 1 Dr. Mohd Kamil Hussain Department of Chemistry Govt. Raza P.G. College Rampur, U.P. India Hyperconjugation Lockdown
  • 2. 222 Hyperconjugation The delocalization of σ-electron in to adjacent π orbital or p-orbital is called hyperconjugation. The contributing structures involving sigma electrons of C - H bond do not show any covalent bond between C and H. Hyperconjugation, therefore, is also called as "no bond resonance" or "Baker-Nathan effect Dr. Mohd Kamil Hussain Requirements for Hyperconjugation: There must be an α-C-H group or a lone pair on atom adjacent to sp2 hybrid carbon or other atoms like nitrogen, oxygen etc. Alkenes, alkyl carbocations, alkyl free radicals, nitro compounds with α- hydrogen.
  • 3. 33 Consequences and Applications of Hyperconjugation Dr. Mohd Kamil Hussain •Stability of alkenes As a general rule, greater the number of α-H of alkyl group attached on the double bond greater is the stability of alkene. With rise in the stability of alkene, the value of heat of hydrogenation deceases
  • 4. Dr. Mohd Kamil Hussain Stability of carbocations : In general, As the number of α-H of alkyl group attached to the positively charged carbon increases, the stability of carbonium ions increases because of increase in the number of contributing structures to hyperconjugation contributing structures to hyperconjugation. Thus the increasing order of stability of carbocations can be given as: methyl < primary < secondary < tertiary as depicted below
  • 5. 5 Stability of free radicals The stability of free radicals is influenced by hyperconjugation just as in case of carbonium ions. Due to hyperconjugation, the stability of free radicals also follow the same order as that of carbonium ions i.e., methyl < primary < secondary < tertiary