The equilibrium constant of mutarotation of -d-glucose to -d-glucose is 1.8. If specific rotation of -d-glucose is 112o and that of mixture is 59o ; what is specific rotation of -d-glucose
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The equilibrium constant of mutarotation of -d-glucose to -d-glucose is 1.8 the rotation of the solution slowly increases from the starting value of + 18.7° to the same equilibrium value of + 54° when -d-glucose dissolves in water.
Mutarotation is the name for this progressive shift in rotation toward an equilibrium point.
- There are two conceivable arrangements for the OH group on the C-1 of sugars. This results in the formation of two stereoisomers, referred to as "anomers": the "-" and the "-" anomers.
- An intriguing thing happens when you test the optical rotation of pure "" or pure "" in water. Over time, the optical rotation gradually changes!
- The observed shift in the optical rotation of the - and - anomers of glucose upon solvent dissolution is referred to as "mutarotation" (literally, "change in rotation").
- The - and - forms gradually interconvert until equilibrium is reached as a result of ring-chain tautomerism.
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