isomerism

There he continued his research on isomerism of the aromatic series.

Now, are there any aspects about the isomerism you want clarifying apart from the whole lot?

This condition usually occasions physical isomerism, with the attendant action on polarized light.

Now the stereo isomerism is all about spatial chemistry, much more than just the way things are attached.

Optical isomerism results when a structure and it's mirror image are non-superimposable.

It is an example of a cycloalkene which exhibits geometric isomerism.

Structural isomerism occurs when the bonds are themselves different.

For example, there may be two (or more) reaction paths for the isomerism above.

Some of his organic research was connected to isomerism of chemical molecules.

An empirical formula makes no reference to isomerism, structure, or absolute number of atoms.

One group of electromers are excited electronic states but isomerism is usually limited to ground state molecules.

Isomerism of the dipolarophile affects reaction rate due to sterics.

Other types of isomerism exist outside this scope.

In position isomerism a functional group or other substituent changes position on a parent structure.

An example of a small hydrocarbon displaying cis/trans isomerism is 2-butene.

Optical isomerism occurs when a molecule is not superimposable with its mirror image.

The only confirmed example of isomerism in bohrium is for the isotope Bh.

Alfred Werner studied the nitro-nitrito isomerism (1 and 2) extensively.

His research in that time was focused on the isomerism of the derivatives of the benzene series.

Usually the rings rotate freely, which simplifies the isomerism.

The symmetry and isomerism of allenes has long fascinated organic chemists.

Most information on conformational isomerism comes from single-crystal X-ray diffraction studies.

Right, let's start with position isomerism.

In larger rings (from around 8 atoms), cis-trans isomerism of the double bond may occur.

A common type of metastability is isomerism.