What is the Difference Between Conjugated and Cumulated Dienes?
🆚 Go to Comparative Table 🆚The main difference between conjugated and cumulated dienes lies in the arrangement of their double bonds and the stability they possess due to resonance.
- Conjugated dienes have two double bonds separated by a single bond, which allows for the sharing of pi electrons across all double bonds, leading to the highest stability among dienes. This conjugation imparts higher stability to the molecule, reducing the electron density on individual double bonds and resulting in resonance. Some reactions of conjugated dienes include the Diels–Alder reaction and additions of polar reagents.
- Cumulated dienes (also called allenes) have two double bonds connected to the same carbon atom, which results in a central carbon atom with sp hybridization and a linear geometry. Cumulated dienes are generally less stable than conjugated dienes because the extended conjugation and delocalization of pi electrons are not possible in this arrangement.
To summarize:
- Conjugated dienes have two double bonds separated by a single bond, leading to stabilization through conjugation and resonance.
- Cumulated dienes have two double bonds connected to the same carbon atom, resulting in a less stable arrangement compared to conjugated dienes.
On this pageWhat is the Difference Between Conjugated and Cumulated Dienes? Comparative Table: Conjugated vs Cumulated Dienes
Comparative Table: Conjugated vs Cumulated Dienes
The main difference between conjugated and cumulated dienes lies in the arrangement of their double bonds. Here is a summary of their characteristics:
Attribute | Conjugated Dienes | Cumulated Dienes |
---|---|---|
Definition | Dienes with two double bonds separated by a single bond | Dienes with two double bonds connected to a similar atom |
Stability | More stable than non-conjugated dienes due to delocalization of charge | Less stable than conjugated dienes |
Heat of Hydrogenation | Lower heat of hydrogenation, indicating higher stability | Higher heat of hydrogenation, indicating lower stability |
Conformations | Adopt "s-cis" and "s-trans" conformations | Not applicable |
Examples | Penta-1,3-diene | 2,3-heptadiene |
Conjugated dienes are more stable than non-conjugated dienes, including cumulated dienes, due to the delocalization of charge in their molecular structure. This stability is reflected in their lower heat of hydrogenation compared to cumulated dienes. On the other hand, cumulated dienes have two double bonds connected to a similar atom, making them less stable.
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