Amide example sentences

"Amide" Example Sentences

1. Acetamide is a derivative of acetic acid.
2. The formation of amide bonds is a common reaction in organic chemistry.
3. Polyacrylamide is a water-soluble amide polymer.
4. The amide functional group is important in biochemistry.
5. Formamide can be used as a solvent and a reactant in chemical synthesis.
6. Amide bonds are found in proteins and peptides.
7. N,N-Dimethylformamide is a common solvent in organic chemistry.
8. The amide functional group contains a carbonyl group bonded to a nitrogen atom.
9. The process of amidation involves the formation of an amide bond.
10. Amides are compounds formed by the reaction of a carboxylic acid and an amine.
11. Succinimide is a cyclic imide with an amide functional group.
12. Thioamides contain a sulfur atom in place of the oxygen atom in amides.
13. Lactams are cyclic amides derived from amino acids.
14. The synthesis of peptides involves the formation of amide bonds between amino acids.
15. Amides have a higher boiling point than alkanes due to hydrogen bonding between molecules.
16. The amide group in proteins is formed between the carboxyl terminus of one amino acid and the amino terminus of another amino acid.
17. Urea is an amide compound found in urine and other body fluids.
18. The polymer Nylon 66 contains alternating amide and alkane groups in its backbone.
19. The structure of amides allows for extensive hydrogen bonding between molecules, leading to high melting and boiling points.
20. Aldehyde groups can react with ammonia to form imines or with primary amines to form amides.
21. Infrared spectroscopy can be used to identify the presence of amide bonds in a compound.
22. Benzamide is an aromatic amide with the molecular formula C7H7NO.
23. Amides are commonly used in organic synthesis as protecting groups for carboxylic acid functional groups.
24. Amides are important building blocks for the synthesis of pharmaceuticals and agrochemicals.
25. The pharmacological properties of many drugs can be attributed to their unique amide functional groups.
26. The solubility of amides in water decreases as the size and complexity of the molecule increases.
27. The amide bond in proteins is relatively stable under physiological conditions, allowing for the formation of complex three-dimensional structures.
28. Amides can undergo hydrolysis in the presence of acid or base, yielding the corresponding carboxylic acid and amine.
29. Secondary amides contain two alkyl or aryl groups bonded to the nitrogen atom.
30. Asparagine is an amino acid that contains an amide functional group in its side chain.

Common Phases

1. Acetamide;
2. Acrylamide;
3. Butyramide;
4. Chloroacetamide;
5. Ethylacetamide;
6. Glycine amide;
7. Hexanamide;
8. Isobutyramide;
9. Methanesulfonamide;
10. N-methylformamide;
11. Propionamide;
12. Succinimide;
13. Thioacetamide.