100 Examples of sentences containing the common noun "heteroatom"

Definition

A heteroatom is any atom in a chemical compound that is not carbon or hydrogen. Common heteroatoms include nitrogen, oxygen, sulfur, phosphorus, and halogens. Heteroatoms are significant in organic chemistry as they influence the chemical properties and reactivity of organic molecules.

Synonyms

• Non-carbon atom
• Non-hydrogen atom
• Functional group atom

Antonyms

• Carbon atom
• Hydrogen atom

Examples

1. In organic compounds, the presence of a heteroatom can greatly affect their properties.
2. Many pharmaceuticals contain at least one heteroatom for enhanced activity.
3. The heteroatom in the molecule provides sites for hydrogen bonding.
4. Chemists often study the role of each heteroatom in a reaction mechanism.
5. The heteroatom in the ring structure alters its stability.
6. Understanding where the heteroatom is located can help predict reactivity.
7. The heteroatom can increase the solubility of an organic compound in water.
8. Heterocycles contain one or more heteroatom in their ring structure.
9. The presence of a heteroatom can change the acidity of a compound.
10. In synthetic chemistry, adding a heteroatom can create new pathways for synthesis.
11. The heteroatom significantly influences the boiling point of the compound.
12. Research on heteroatom incorporation is essential for developing new materials.
13. The stability of the compound can be affected by the type of heteroatom present.
14. A heteroatom in a polymer can introduce valuable properties.
15. The heteroatom plays a key role in the reactivity of nucleophiles.
16. Many natural products contain a heteroatom in their structures.
17. The heteroatom can participate in various types of bonding.
18. In medicinal chemistry, the heteroatom is often a target for modifications.
19. The heteroatom can affect the color of a compound.
20. A compound's polarity may change due to the presence of a heteroatom.
21. The heteroatom may serve as a site for functionalization in organic synthesis.
22. In coordination chemistry, the heteroatom can coordinate with metal centers.
23. The heteroatom contributes to the overall electronic distribution in the molecule.
24. The introduction of a heteroatom can enhance the biological activity of a compound.
25. Many organic reactions involve a heteroatom acting as a nucleophile.
26. The heteroatom can stabilize charged intermediates during a reaction.
27. Analyzing the heteroatom distribution helps in understanding molecular behavior.
28. The heteroatom can create steric hindrance in a molecule.
29. The heteroatom may affect the fluorescence of certain compounds.
30. The heteroatom in the substrate can influence catalyst design.
31. A heteroatom can be introduced using various synthetic routes.
32. The heteroatom can dictate the solubility of the compound in different solvents.
33. The presence of a heteroatom often leads to unique spectroscopic features.
34. The heteroatom may be involved in the formation of intermolecular forces.
35. Understanding the role of each heteroatom is crucial in reaction optimization.
36. The heteroatom can affect the rate of reaction in organic transformations.
37. The heteroatom may alter the reactivity of functional groups.
38. In many cases, the heteroatom can stabilize transition states.
39. The heteroatom can influence the overall geometry of the molecule.
40. The heteroatom often plays a role in determining the acidity or basicity.
41. The heteroatom can be a target for selective modification in drug design.
42. The heteroatom can introduce chirality into a molecule.
43. The heteroatom may form complexes with transition metals.
44. The heteroatom can facilitate electron transfer in redox reactions.
45. The heteroatom often creates reactive intermediates in synthetic pathways.
46. The heteroatom can influence the molecular weight of the compound.
47. The heteroatom may participate in hydrogen bonding with solvent molecules.
48. The heteroatom can affect the thermal stability of the compound.
49. The heteroatom often determines the nature of the reaction.
50. The heteroatom can impact the molecular orbitals of the compound.
51. The heteroatom can enhance the reactivity of electrophiles.
52. The heteroatom might be involved in catalytic cycles.
53. The heteroatom can play a pivotal role in the mechanism of action of drugs.
54. The heteroatom often determines the compatibility with biological systems.
55. The heteroatom can introduce functional diversity in organic molecules.
56. The heteroatom can help stabilize radical species.
57. The heteroatom can influence the energy levels of molecular orbitals.
58. The heteroatom can affect the interaction of molecules with light.
59. The heteroatom can contribute to the overall reactivity of the compound.
60. The heteroatom can be strategically placed to enhance synthetic pathways.
61. The heteroatom can serve as a point of attachment for other groups.
62. The heteroatom can impact the specificity of biochemical reactions.
63. The heteroatom may lead to the formation of new bonds during reactions.
64. In polymer chemistry, the heteroatom can modify the polymer's properties.
65. The heteroatom can improve the stability of reaction intermediates.
66. The heteroatom can affect the viscosity of a solution.
67. The heteroatom can alter the physical properties of the compound.
68. The heteroatom can serve as a substituent in aromatic systems.
69. The heteroatom plays a critical role in enzyme catalysis.
70. The presence of a heteroatom can enhance the reactivity of alkenes.
71. The heteroatom can participate in complexation reactions.
72. The heteroatom can modify the electrochemical properties of a compound.
73. The heteroatom can influence the stability of the drug candidate.
74. The heteroatom can dictate the interaction with target biomolecules.
75. The heteroatom can affect the pharmacokinetics of a drug.
76. The heteroatom can introduce new functionalities in synthetic chemistry.
77. The heteroatom can enhance the lipophilicity of compounds.
78. The heteroatom can alter the pKa of acidic or basic functional groups.
79. The heteroatom can direct the outcome of a chemical reaction.
80. The heteroatom can cause changes in the melting point of a solid.
81. The heteroatom often plays a role in defining the reactivity of heterocycles.
82. The heteroatom can stabilize certain reaction pathways.
83. The heteroatom can influence the formation of coordination complexes.
84. The heteroatom can enhance the solubility of poorly soluble drugs.
85. The heteroatom can affect the selectivity of catalysts.
86. The heteroatom can participate in the formation of cyclic structures.
87. The heteroatom can alter the rate of degradation in biological systems.
88. The heteroatom can enhance the effectiveness of insecticides.
89. The heteroatom can assist in the formation of stable intermediates.
90. The heteroatom can affect molecular interactions in biological pathways.
91. The heteroatom can be used to create new materials with tailored properties.
92. The heteroatom can introduce new pathways for drug metabolism.
93. The heteroatom can play a role in the formation of drug-drug interactions.
94. The heteroatom can dictate the stability of organometallic compounds.
95. The heteroatom can influence the design of molecular sensors.
96. The heteroatom can participate in the formation of supramolecular structures.
97. The heteroatom can affect the kinetics of chemical reactions.
98. The heteroatom can enhance the stability of reactive intermediates.
99. The heteroatom can be a critical component in the synthesis of complex molecules.
100. The heteroatom can help in the creation of biodegradable plastics.