Home
Class 12
CHEMISTRY
Mutarotation is the change in specific r...

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon
`alpha-`glucose and `beta-`glucose differ in configuration at ______ and are called

A

`C_(1)`, Anomers

B

`C_(2)`, Anomers

C

`C_(2)`, Epimers

D

`C_(3)`, Tautomers

Text Solution

Verified by Experts

The correct Answer is:
A
Mutarotation
Promotional Banner

Topper's Solved these Questions

  • CARBOHYDRATES

    AAKASH SERIES|Exercise Level -II Lecture Sheet (Exercise-III)|4 Videos

  • CARBOHYDRATES

    AAKASH SERIES|Exercise Level -II Lecture Sheet (Exercise-IV)|4 Videos

  • CARBOHYDRATES

    AAKASH SERIES|Exercise Level -II Lecture Sheet (Exercise-I)|20 Videos

  • BIOMOLECULES

    AAKASH SERIES|Exercise OBJECTIVE EXERCISE-4 (ASSERTION (A) & REASON (R) TYPE QUESTIONS :)|84 Videos

  • CARBOXYLIC ACIDS

    AAKASH SERIES|Exercise PRACTICE SHEET-4 (Integer Type Questions)|9 Videos

Similar Questions

Explore conceptually related problems

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon The anomeric carbon in fructose is

Mutarotation is the change in specific rotation of an optically active compound in solution with time to an equilibrium value. Interconversion is possible only if sugar has anomeric hydroxyl group i.e., sugar is reducing. Diastereomers which differ in configuration of chiral carbon developed in hemiacetal formation are called anomers. Epimers are a pair of stereoisomers which differ in the configuration about one of its chiral carbon On which carbon atom glucose and galactose differ in the position of -H and -OH groups?

Configuration of a chiral molecule can be changed by

The amino acid without chiral carbon is

Accroding to CIP rules, the configuration of chiral carbon atoms in D - (+) - glucose are

The number of Chiral carbons in alpha -D-Glucose are _______

According to CIP rules, the configuration of chircal carbon atoms in D (+) glucose are

The general electronic configuration of carbon group elements is

Inert gas element which has a different valence shell configuration

Which is a reducing sugar?