to form pyranose the hydroxyl group from which position of an aldohexose attacks the carbonyl carbon
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To form the pyranose, the hydroxyl group at the fifth (5) position of an aldohexose attacks the carbonyl carbon.
- The hydroxyl at the 5 position forms a hemiacetal with the aldehyde at the position one (1).
- In other words, the pyranose ring structure is formed due to hemiacetal formation between C₁ and C₅ carbon atoms.
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