And at various stages during the organic you'll also be coming to what we call optical isomers.

It is a mixture of four optical isomers which have different insecticidal activities.

Lactic acid is chiral and has two optical isomers.

That's the name for optical isomers.

Two mirror images of a chiral molecule are called enantiomers or optical isomers.

Hence, acetylmethadol has four possible optical isomers.

The racemic mixture can be divided into its optical isomers: levo- and dextro-amphetamine.

While still a graduate student, he patented the method that is used to make the optical isomers of hallucinogenic amphetamines.

Chemists call these enantiomers or optical isomers.

There are many substances encompassed under this general name (9 structural isomers, 5 of which have optical isomers).

In this system too the presence of enantioenriched catalyst drives the reaction towards one of the two possible optical isomers.

You know, optical isomers, alright?

For example, two molecules may be non-superimposible mirror images, in which case the pair of molecules are referred to as "optical isomers".

This also makes macroscopic crystals of the pair of optical isomers mirror images of one another.

Optical isomers can have different detections thresholds since their conformations may cause them to be less perceivable for the human nose.

Pure optical isomers can be obtained by hydration of optically pure propylene oxide.

Cathine is one of the optical isomers of phenylpropanolamine (PPA).

I programmed it as a comparator of optical isomers for a first step in trying to detect where and how our instincts are imprinted on us."

And in the case of organic compounds the crystal structure of optical isomers can result in different crystal structures.

The classic example here is tartaric acid optical isomers separated by Louis Pasteur with tweezers under a microscope.

This means that optical isomers partition identically into lipid, but have differential effects on ion channels and synaptic transmission.

He resolved the first coordination complex called hexol into optical isomers, overthrowing the theory that chirality was necessarily associated with carbon compounds.

The optical isomers (+) limonene and (-) limonene are the characteristic odors of orange and lemon respectively.

Catechin and epicatechin are epimers, with (-)-epicatechin and (+)-catechin being the most common optical isomers found in nature.

As observed in all subsequent experiments, both left-handed (L) and right-handed (D) optical isomers were created in a racemic mixture.