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Conjugated dienes are more stable than isolated dienes due to delocalization of pi electrons across the double bonds in the conjugated system. This delocalization lowers the overall energy of the system, making it more stable. In contrast, isolated dienes have localized pi electrons which do not benefit from this delocalization and are therefore less stable.

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Why cumulative dienes are less stable than isolated?

Cumulative dienes, which have two double bonds adjacent to each other, are less stable than isolated dienes due to increased electron repulsion and steric strain between the overlapping π bonds. This proximity makes the double bonds more reactive and less stable compared to isolated dienes, where the double bonds are separated by at least one single bond, allowing for greater spatial separation and reduced electron repulsion. Additionally, cumulative dienes lack the resonance stabilization that can be present in isolated dienes, further contributing to their lower stability.


What are the three types of alkadienes?

Cumulated dienes have the double bonds sharing a common atom as in a group of compounds called allenes.Conjugated dienes have conjugated double bonds separated by one single bond.Unconjugated dienes have the double bonds separated by two or more single bonds. They are usually less stable than isomeric conjugated dienes. This can also be known as an isolated diene.


What are the key differences between antiaromatic and nonaromatic compounds in terms of their electronic structures and aromaticity?

Antiaromatic compounds have a fully conjugated ring system with 4n electrons, making them highly unstable and reactive. Nonaromatic compounds do not have a fully conjugated ring system or have an odd number of electrons, making them more stable. Aromatic compounds have a fully conjugated ring system with 4n2 electrons, making them stable and less reactive than antiaromatic compounds.


Comparison of stability of 1 2- benzylethene and 1- benzylethene?

Benzyl ethene is not a proper name it means 3-phenyl propene similarly 1,2 dibenzyl ethene means 1,4 diphenyl -2- butene, the later is more stable due to possibilities of more resonating structures.


What is a graph of isolated points?

It is a graph of isolated points - nothing more, nothing less!


When atoms combine to form compound do they become more stable or less stable?

More stable


Why 13-cis lycopene more stable than 7-cis and 11-cis?

13-cis lycopene is more stable than 7-cis and 11-cis because it has a more extended conjugated system, making it less prone to isomerization and oxidation. The increased delocalization of electrons in 13-cis lycopene results in higher stability compared to 7-cis and 11-cis isomers.


What is a more stable atom between lithium and gold?

Gold is more stable.


Is olivine more stable and weathering faster than quartz?

Following Goldich Dissolution Series (Or going backwards by Bowen's Reaction Series), olivine weathers before Quartz. Quartz has a framework silicate structure and olivine has a isolated silicate structure.


What is meant by resonance stabilized?

Resonance stabilization refers to the delocalization of electrons in a molecule through different possible resonance structures. This distribution helps to lower the overall energy of the molecule, making it more stable. Resonance stabilization is commonly seen in molecules with conjugated systems, such as in aromatic compounds like benzene.


How stable is the UK?

A t least as stable as, say, the USA or Canada, if not more stable. More stable than Iran, Iraq, Pakistan, Afghanistan, Congo. But not as stable as Saudi Arabia, UAE, Oman, Qatar.


What is the formula for conjugate base of acid HS?

Remember that a conjugated acid has one proton H+ more than the (conjugated) base of it.So H2S is conjugated as acidto the base HS- .