Iodobenzene example sentences

"Iodobenzene" Example Sentences

1. Iodobenzene is a crucial reagent in many organic syntheses.
2. The reaction yielded a significant amount of iodobenzene.
3. We analyzed the iodobenzene using gas chromatography.
4. Purification of the iodobenzene proved challenging.
5. The synthesis of iodobenzene requires careful control of temperature.
6. Impurities in the iodobenzene affected the final product.
7. Iodobenzene, a key intermediate, was readily prepared.
8. The NMR spectrum confirmed the presence of iodobenzene.
9. Excess iodobenzene was removed by washing.
10. Further studies are needed to understand the reactivity of iodobenzene.
11. A significant yield of iodobenzene was obtained under optimized conditions.
12. The coupling reaction with iodobenzene proceeded smoothly.
13. Iodobenzene reacted readily with the Grignard reagent.
14. The use of iodobenzene in this reaction is well-established.
15. We observed a high conversion to iodobenzene in this experiment.
16. The properties of iodobenzene make it suitable for this application.
17. Iodobenzene served as a starting material for the synthesis.
18. The researchers successfully synthesized iodobenzene with high purity.
19. Unexpectedly, the reaction produced iodobenzene as a byproduct.
20. Analysis revealed the presence of trace amounts of iodobenzene.
21. Iodobenzene, although expensive, proved essential.
22. The reaction with iodobenzene required anhydrous conditions.
23. Iodobenzene's reactivity is influenced by its electronic properties.
24. Careful handling of iodobenzene is necessary due to its toxicity.
25. The yield of iodobenzene was significantly improved by this modification.
26. We compared the reactivity of iodobenzene with bromobenzene.
27. Iodobenzene is a colorless liquid at room temperature.
28. The synthesis of iodobenzene involved a diazonium salt intermediate.
29. This method provides a convenient synthesis of iodobenzene.
30. The characterization of iodobenzene was performed using various techniques.
31. The article discussed the applications of iodobenzene in medicinal chemistry.
32. Iodobenzene is a versatile building block in organic chemistry.
33. With iodobenzene, the reaction proceeded efficiently.
34. The presence of iodobenzene was confirmed by mass spectrometry.
35. Iodobenzene's density is greater than that of water.
36. Using iodobenzene, we synthesized a novel derivative.
37. The reaction involving iodobenzene was catalytic.
38. Iodobenzene is commercially available in high purity.
39. A new method for the synthesis of iodobenzene was developed.
40. The cost of iodobenzene is a factor to consider.
41. The team found that iodobenzene was superior to other reagents.
42. Iodobenzene, being less reactive, gave a cleaner product.
43. Despite its toxicity, iodobenzene is widely used.
44. The shelf life of iodobenzene is relatively long.
45. Iodobenzene is susceptible to decomposition under certain conditions.
46. They investigated the mechanism of reaction with iodobenzene.
47. Iodobenzene dichloride is a related compound.
48. The experiment required precisely measured amounts of iodobenzene.
49. The purification process removed all traces of iodobenzene.
50. Further research into the applications of iodobenzene is warranted.

Common Phases

1. Iodobenzene diazonium salt formation is a crucial step.
2. Iodobenzene's reactivity in cross-coupling reactions is well-documented.
3. Iodobenzene undergoes facile palladium-catalyzed coupling.
4. The synthesis of iodobenzene often involves iodine-mediated reactions.
5. Iodobenzene is a versatile building block in organic synthesis.
6. Electrophilic aromatic substitution on iodobenzene is relatively slow.
7. Purification of iodobenzene typically involves distillation.
8. The NMR spectrum of iodobenzene shows a characteristic peak.
9. Analyzing the GC-MS of iodobenzene confirms its purity.
10. Iodobenzene's higher boiling point requires careful handling.
11. The yield of iodobenzene in this reaction is moderate.
12. Iodobenzene is a key intermediate in this multi-step synthesis.
13. Storage of iodobenzene should be under inert atmosphere and away from light.
14. The preparation of iodobenzene demands specific reaction conditions.
15. Compare the reactivity of iodobenzene with other aryl halides.
16. Consider the steric hindrance around iodobenzene during reactions.
17. The stability of iodobenzene allows for extended reaction times.
18. Iodobenzene serves as an excellent substrate for various reactions.
19. Monitor the reaction progress of iodobenzene using TLC.
20. Iodobenzene's cost-effectiveness makes it suitable for large-scale synthesis.