
Define the term hyperconjugation.
Answer
477.3k+ views
Hint: We know that in organic chemistry, electron displacement plays a vital role for chemical and physical properties of the molecule. Inductive effect, electromeric effect and hyperconjugation are important electron displacement effects in organic molecules. Some of these effects show permanent and temporary effects in molecules.
Complete step by step answer:
We have to remember that in organic molecules most of them are formed by covalent bonds. These covalent bond are classified as two types
There are
1.Sigma bond
2.Pi bond
We need to know that the mutual sharing two electrons in between two atoms, overlapping orbitals to form sigma and pi bond. Sigma bond means overlapping in head to head overlap in orbitals. Pi bond means overlapping occurs side wise in orbitals.
We need to know that hyperconjugation is one of the displacements of the electron in organic chemistry. The delocalisation of the sigma electron in bond is known as hyperconjugation. This hyperconjugation gives the special stability of the molecule, because one sigma electron delocalisation to form bonding or antibonding pi bond in conjugated carbon atom. This hyperconjugation is also called “no bond resonance”.
For example, propene having three canonical forms due to hyperconjugation. An electron in sigma bond is changed to form a pi bond ( ) in conjugated carbon atoms. In this hyperconjugation three resonance structures arise to increase the stability of propene.
Note: We need to know that the stability of the carbocation is dependent on the hyperconjugation. The tertiary carbocation is more stable than secondary and primary carbocation. The hyperconjugation to produce the various resonance structures of the one molecule. The more resonance structure possible in one molecule means that molecule is more stable. This stability is used to identify by the substitution reaction in the molecules. Hyperconjugation is a permanent effect in the molecule. In some reactions, hyperconjugation is known as the “Baker-Nathan effect”.
Complete step by step answer:
We have to remember that in organic molecules most of them are formed by covalent bonds. These covalent bond are classified as two types
There are
1.Sigma bond
2.Pi bond
We need to know that the mutual sharing two electrons in between two atoms, overlapping
We need to know that hyperconjugation is one of the displacements of the electron in organic chemistry. The delocalisation of the sigma electron in bond is known as hyperconjugation. This hyperconjugation gives the special stability of the molecule, because one sigma electron delocalisation to form bonding or antibonding pi bond in conjugated carbon atom. This hyperconjugation is also called “no bond resonance”.
For example, propene having three canonical forms due to hyperconjugation. An electron in

Note: We need to know that the stability of the carbocation is dependent on the hyperconjugation. The tertiary carbocation is more stable than secondary and primary carbocation. The hyperconjugation to produce the various resonance structures of the one molecule. The more resonance structure possible in one molecule means that molecule is more stable. This stability is used to identify by the substitution reaction in the molecules. Hyperconjugation is a permanent effect in the molecule. In some reactions, hyperconjugation is known as the “Baker-Nathan effect”.
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