The specific rotation for
`alpha-D-" glucose "= +112^(@)`
For `beta-D-" glucose "= +19^(@)`
An equilibrium mixture containing `alpha" and "beta`- forms has specific rotation of `+52.7^(@)C`. Calculate the % composition of the different anomers.

The optical rotation of the alpha -form of a pyranose is +150.7^(@) , that of the beta -form is +52.8^(@) . In solution an equilibrium mixture of these anomers has an optical rotation of +80.2^(@) . The precentage of the alpha -form in equilibrium mixture is :

alpha-D- glucose and beta-D- glucose are enantiomers. True/False

Equimolar mixture of alpha -D(+)-glucose has specific ([alpha]_(D)) is

How much of the alpha -anomer and beta -anomers are present in an equilibrium mixture with a specific rotation of +52.6^(@) ?

alpha-(D)" glucose "hArr beta-(D) glucose, equilibrium constant for this s 1.8. The percentage of alpha-(D) glucose at equilibrium is

The specific rotation of two glucose anomers are alpha = + 110^(@) and beta = 19^@ and for the constant equilibrium mixtures is +52.7^@ . Calculate the percentage compositions of the anomers in the equilibrium mixture.

alpha -D(+)-glucose and beta -D(+) glucose are

A 10 g mixture of glucose and urea present in 250 mL solution shows the osomotic pressure of 7.4 atm at 27^(@)C . Calculate % composition of mixture.

Rapid interconversion of alpha -D-Glucose and beta -D-Glucose in solution is known as: