Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

28. Carbohydrates

Monosaccharides - Forming Cyclic Hemiacetals

Organic Chemistry

28. Carbohydrates

Monosaccharides - Forming Cyclic Hemiacetals

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Multiple Choice

When monosaccharides form cyclic hemiacetals, which type of molecule is released during the linkage process?

Carbon dioxide

Water

Methane

Oxygen

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Verified step by step guidance

Understand that monosaccharides can form cyclic structures through a reaction between the hydroxyl group and the carbonyl group within the same molecule, resulting in a hemiacetal formation.

Recognize that during the formation of a cyclic hemiacetal, a new bond is formed between the carbonyl carbon and the oxygen of the hydroxyl group, creating a ring structure.

Identify that this process involves the removal of a small molecule as a byproduct of the reaction.

Recall that in organic chemistry, the formation of acetals and hemiacetals typically involves the release of a water molecule (H₂O) as the hydroxyl group (OH) and a hydrogen atom (H) from the carbonyl group combine.

Conclude that the molecule released during the formation of cyclic hemiacetals from monosaccharides is water (H₂O), as it is a common byproduct in such condensation reactions.