Questions tagged [hyperconjugation]

Hyperconjugation involves the donation of electrons from a filled orbital (commonly the bonding C-H sigma molecular orbital) into an adjacent/partially occupied p-orbital (for instance an adjacent carbocation) leading to stabilisation. The tag should be applied to questions where hyperconjugation is involved, even if the question does not explicitly refer to it.

Hyperconjugation involves the donation of electrons from a filled orbital (commonly the bonding C-H sigma molecular orbital) into an adjacent/partially occupied p-orbital (for instance an adjacent carbocation) leading to stabilisation.

In organic chemistry, hyperconjugation is used to explain the increased stability of alkyl-substituted radicals/carbocations and has been invoked in explanations of the anomeric and beta-silicon effects.

Definition:

IUPAC Gold book

In the formalism that separates bonds into sigma and pi types, hyperconjugation is the interaction of sigma-bonds (e.g. C–H, C–C, etc.) with a pi network. This interaction is customarily illustrated by contributing structures, e.g. for toluene (below), sometimes said to be an example of 'heterovalent' or 'sacrificial hyperconjugation', so named because the contributing structure contains one two-electron bond less than the normal Lewis formula for toluene:

Applicability of the tag:

  • will almost always be applied with the tag as the stabilising effect is observed in organic molecules. also fits since the hyper conjugative effect is a result of bonding MO’s donating electron density. It should be applied even if the OP does not realise that hyperconjugation is involved (for instance questions blindly asking why certain cations are stabilised relative to others).
  • additional tags may be applied depending on the nature of the question, such as if discussing the way in which hyperconjugation stabilises a carbocation for example. may also be relevant.

Related tags:

The following tags are related to , with multiple questions on chemistry.se already tagged with one of more of the following which may be useful as additional tags on questions identified as being related to medicinal chemistry:

Further reading:

Hyperconjugation is quite a narrow topic but is covered by many organic chemistry texts (see for references).

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Why does hyperconjugation help for ring cleavage?

The question was to rationalize it the ring cleavage happens concerted or non-concerted. The papers "The Mechanism of the Thermal Decomposition of 1-Pyrazolines and Its Relationship to Cyclopropane Isomerizations" (Crawford 1965/1966; Original…
laminin
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Gauche effect and bond length

Which of the following compounds has the longest bond length? (A) $\ce{H3C-CF3}$ (B) $\ce{FCH2-CH2F}$ (C) $\ce{F2CH-CHF2}$ (D) $\ce{F3C-CF3}$ My logic was based on the relative electronegativities of the two carbons. The more fluorines there are…
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Why are tertiary carbocations so stable?

Today our lecturer provided this data to illustrate the relative stability of carbocations. \begin{array}{|c|c|c|c|c|} \hline \text{Substrate} & \ce{t-BuBr} & \ce{i-PrBr} & \ce{EtBr} & \text{MeBr}\\ \hline \mathrm{Relative~rate~of~S_N1~reaction} &…
bon
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The effect of hyperconjugation on the stability of alkenes with MO theory

Hyperconjugation stabilizes carbocations and that makes sense because electrons are given to the empty p orbital. But how does it stabilize alkenes? Can molecular orbital theory be used to explain it?
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Inductive effect and hyperconjugation - one elephant, different parts?

Are the inductive effect and hyperconjugation both different ways of looking at the same phenomenon - i.e. methyl groups donate negative charge for example. Inductively we can argue that carbon is of greater electronegativity than hydrogen, and so…
Dissenter
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What is hyperconjugation?

What is hyperconjugation and how do you know if there is hyperconjugation in a compound? Which orbitals are involved in hyperconjugation?
Maneesh Dev
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What is the directive influence of the tert-butyl group in electrophilic aromatic substitution?

We know that hydrocarbon side-chains on a benzene ring influence electrophilic substitutions by directing the incoming electrophile to attack at ortho and para positions. The following hyperconjugations are shown to explain directive effect of…
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Why is the eclipsed conformer more stable than the bisected conformer in 1-butene?

I have just started learning conformational analysis, and a major doubt came into my mind. In simple alkanes such as ethane, the staggered conformer is much more stable than the eclipsed conformer. This fact may be explained as follows: In the…
Newton
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How does hyperconjugation affect bond lengths in alkenes?

How does the number of hyperconjugates affect the $\ce{C=C}$ bond length in the compounds propene and 3,3-dimethylbut-1-ene? In general, is bond length directly or inversely proportional to the number of hyperconjugates?
Jay Gitz
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Why is a C–D bond stronger than a C–H bond?

I have heard that the carbon–deuterium bond is stronger than the carbon–hydrogen bond. What are the possible reasons for it? Is this also the reason that C–H bonds participate more in hyperconjugation than C–D bonds? Please explain.
Kartikeya Badola
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How to compare stability between 5‐methylcyclohexa‐1,3‐diene and 3‐methylenecyclohexene?

Problem Compare stability of 1 and 2: Answer 1 is more stable than 2. My approach Both have the same number of π-bonds. Both have one resonance structure. Both are non-aromatic. In 1 there are three α-hydrogens, whereas in 2 there are four…
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Hyperconjugation in ethane conformers

I refer you to this set of presentation slides. On slide 8, the author explains the preference for the staggered conformation of ethane by saying that there is a favourable hyperconjugative interaction between $\sigma^{}_{\ce{C-H}}$ of the…
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Hyperconjugation in cresol

In cresol both $+I$ effect as well as hyperconjugation work together to determine its acidity. When the methyl group is present in the ortho- and para-position both of them can act upon phenol. Hyperconjugation as a rule dominates which increases…
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Why are double bonds at more substituted carbon more stable?

That $\ce{C=C}$ bonds are more stable at more substituted carbon atoms is a common argument used throughout Clayden et al., but is never actually explained (at least not in the first 21 chapters). They do explain however, why the HOMO is increased…
Jori
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Why are the unsaturated fatty acids usually unconjugated?

My textbook gives the structures of the unsaturated fatty acids in food including oleic acid, linoleic acid, linolenic acid and docosatetraenoic acid. I figure that when two or more $\ce{C=C}$ double bonds appear in a fatty acid, they tend to…
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