Organic Chemistry/Dienes/Diene properties and reactions
Organic chemistry > Dienes >Diene Properties and Reactions
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Common Reactions of Conjugated Dienes edit
Conjugated dienes have enhanced stability as compared to molecules without conjugated double bonds due to resonance. In general, this makes them slightly less reactive than other types of alkenes in general and dienes specifically. However, many reactions proceed through high-energy cation or radical intermediates; in these cases the resonance stabilization of the intermediate allyl species makes conjugated dienes more reactive than non-conjugated dienes or simple alkenes.
Hydrobromination: edit
Adds a Bromine and a Hydrogen to a conjugated Diene.
Example:
Butadiene + HBr--> 3-bromobutene (Low Temperature) + 1-bromobut-2-ene (High Temperature) + 1-bromobutene (Not Observed)
Thermodynamic and Kinetic Control of Reaction:
- At low temperature the reaction is under KINETIC CONTROL: the 3-bromobutene is formed faster because it has a lower transition state free energy, as the intermediate cation is more stable at the secondary carbon.
- At high temperature the reaction is under THERMODYNAMIC CONTROL: the 3-bromobutene still forms more quickly, but the reaction has enough energy to reverse, and the more stable product (1-bromobut-2-ene) is formed.
Diels-Alder Reaction edit
One of the most important of all diene reactions is the Diels-Alder Reaction, in which a conjugated diene reacts with an dienophile to form a cyclohexene.
Requirements:
The diene must be able to access the s-cis conformation for the reaction to take place.
DIENEOPHILES - A species which likes to attack Dienes
- A Dienophile must contain a double or triple bond. Typically, an electron withdrawing group is conjugated to the dienophile to make it electron-poor (nitriles, ketones, and esters are common electron withdrawing groups). Because the reaction is highly stereospecific, the configuration of the dieneophile will determine the relative stereochemistry of the cyclohexene product.
The Diels-Alder reaction occurs most effectively with an electron-poor dieneophile and an electron-rich diene ('normal demand'). 'Inverse demand' Diels-Alder reactions can also be carried out, in which the dienophile is electron-rich and the diene electron-poor.