Heteroatom

The chemical properties of a heterocyclic compound depend on the nature of its heteroatom.

The heteroatom in the molecule can affect its solubility in different solvents.

The heteroatom in the molecule is responsible for its acidic properties.

The introduction of a heteroatom into a polymer can alter its physical properties.

The heteroatom in the heteropolyacid enhances its catalytic activity.

The protein contains a sulfur heteroatom in its active site.

Oxygen is a common heteroatom found in organic molecules.

The heteroatom nitrogen is present in most organic bases.

The nitrogen heteroatom in the molecule is responsible for its basicity.

The presence of a heteroatom in the compound increases its polarity.

The heteroatom in the molecule can act as a nucleophile in organic reactions.

The heteroatom in this DNA base pair is responsible for its hydrogen bonding with the complementary base pair.

The reactivity of this organic compound is determined by the presence of a heteroatom.

The heteroatom in the pesticide molecule determines its specificity for pests.

The heteroatom in this particular compound is responsible for its unique odor.

The heteroatom oxygen is responsible for the acidic properties of furan.

The heteroatom in the molecule determines its biological activity.

The heteroatom sulfur plays a key role in the function of certain enzymes.

The heteroatom nitrogen is commonly found in many pharmaceutical compounds.

The heteroatom in the drug molecule is responsible for its therapeutic effects.

The heteroatom oxygen in this molecule is responsible for its ability to form hydrogen bonds with water molecules.

The heteroatom nitrogen gives pyridine its characteristic basicity.

The heteroatom in the fragrance molecule contributes to its unique aroma.

The nitrogen heteroatom in pyridine gives it a basic character.

The oxygen heteroatom in the carbonyl group of acetone allows it to participate in hydrogen bonding.

The nitrogen heteroatom in caffeine is responsible for its stimulating effect.

The heteroatom in this molecule is bonded to four other atoms, giving it a different shape than the rest.

The heteroatom in this molecule has a lone pair of electrons.

The heteroatom chlorine is used in the production of many industrial chemicals.

The heteroatom in this pesticide molecule makes it more effective against pests.

The heteroatom in this polymer chain affects its physical and chemical properties.

The drug contains a heteroatom that makes it more effective against bacteria.

The nitrogen heteroatom is the key functional group in this class of molecules.

The heteroatom sulfur in the molecule is responsible for the garlic-like odor.

The presence of a heteroatom can affect the physical properties of the compound, such as its melting point.

The nitrogen heteroatom in pyridine makes it a basic molecule.

The presence of a heteroatom in a molecule can affect its physical properties such as melting point and boiling point.

The reactivity of a heteroatom in a molecule can be altered by changing its electronic environment.

The heteroatom in the polymer backbone imparts unique properties to the material.

This metal complex has a heteroatom that coordinates to the metal ion.

The nitrogen heteroatom in caffeine gives it its stimulating effects.

The presence of a nitrogen heteroatom in the compound is necessary for its biological activity.

Oxygen is a common heteroatom in many organic molecules.

The heteroatom in a molecule can influence its biological activity and pharmacological properties.

The presence of a heteroatom in the molecule increases its polarity.

The heteroatom in the molecule determines its reactivity with other compounds.

The sulfur heteroatom in cysteine is important for its role in protein structure.

Nitrogen is a heteroatom present in the amino acids that make up proteins.

The heteroatom in a molecule can be identified using various spectroscopic techniques.

The heteroatom in the molecule can act as a Lewis base.