alkene

What has been debated is the coordination of the alkene.

The major alkene product is formed in over 90% yield.

Even if the reaction is performed cold, some alkene may be formed.

Rather it results in the production of a ketone with an alkene group.

This is the process that results in the alkene products of steam cracking.

These molecules are put together with a double bond that makes it an alkene.

High reactivity of the activated alkene could also be a problem.

The molecule is unsaturated at position 5,6 with an alkene group.

Oxymercuration is not limited to an alkene reacting with water.

The alkene portion of the molecule is reactive in many ways.

This reaction can be used to determine the position of a double bond in an unknown alkene.

At about 200 C, the alkene is formed by an intramolecular elimination.

In a group of related worker bees, half were injected with an alien alkene.

The nitro compound may be aromatic rather than just an alkene.

When using a rhodium catalyst, it is difficult to stop the reaction at the alkene stage.

An alkene's unsaturation means that it will take the color out of bromine.

As a result, this reaction often generates a mixture of alkene stereoisomers.

The reaction mechanism for an alkene bromination can be described as follows.

The values for the alkane, alkene and alkyne families were 10 times greater than average.

Oxymercuration-reduction is another reaction that converts an alkene into an alcohol.

The directly-attached atoms on a simple alkene are all coplanar.

It is composed of both alkyne and alkene groups.

In the transition state for cyclization, the small substituent points toward the alkene.

The less hindered faces of the enone and alkene react.

Thus, coordination of the alkene does not require ligand dissociation.