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The specific rotation of a pure enantiom...

The specific rotation of a pure enantiomer is `+10^(@)`. The observed rotation, if it is isolated from a reaction with `30%` recemisation and `70%` inversion is

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The specific rotation of a pure enantiomer is +16^@ . The observed rotation, if it is isolated from a reaction with 25% racemisation and 75% inversion is

The specific rotation of a pure enantiomer is +16^@ . The observed rotation, if it is isolated from a reaction with 25% racemisation and 75% inversion is

The specific rotation of a pure enantiomer is +10^(@) . What will be its observed rotation if its is isolated from a reaction with i. 30% racemisation and 70% retention. ii. 70% racemisation and 30% inversion.

a. The specific rotation of a pure enantiomer is +10^(@) . What will be its observed rotation if its is isolated from a reaction with i. 30% racemisation and 70% retention. ii. 70% racemisation and 30% inversion. b. What is the percentage composition of a mixtrue of two enantiomers whose rotation is -10^(@) ? The specific rotation of pure enantiomers is -20^(@) . c. What is the optical purity of a sample having an [alpha]_(obs.)=+9.0^(@) if [alpha]_(D)=+12^(@) .

The specific rotation of a pure enantiomer is +16^(@) its observed rotation if it is isolated from a reaction with 25% racemisation and 75% retention is,

The specific rotation of a pure enantiomers is +12^(@) . What will be its observed rotation if it is isolated form a reaction with 80% racemization and 20% inversion.

The specific rotation of a pure enantiomers is +12^(@) . What will be its observed rotation if it is isolated form a reaction with 20% racemization and 80% retention.

An organic compound P exists in two enantiomeric forms, which have specific optical rotation values [alpha] = +-100^(@) . The optical rotation of a mixture of these two enantiomers is -50^(@) . Calculate the percentage of that enantiomer which is in lower concentration in the mixture.

(+) Mandelic acid has a specific rotation of +158^@ . What would be the observed rotation of a mixture of 30% (-) mandelic acid and 70% (+) mandelic acid